| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | C J Hueck | |
| P2860 | cites work | Sequence analysis of a cDNA encoding a human nuclear pore complex protein, hnup153 | Q24324042 |
| Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold | Q24556499 | ||
| Gentamicin antibacterial activity in the presence of human polymorphonuclear leukocytes | Q24597159 | ||
| ABC transporters: bacterial exporters | Q24634629 | ||
| Common themes in microbial pathogenicity revisited | Q24643808 | ||
| Differential effects of deletions in lcrV on secretion of V antigen, regulation of the low-Ca2+ response, and virulence of Yersinia pestis | Q24673488 | ||
| Analysis of virC, an operon involved in the secretion of Yop proteins by Yersinia enterocolitica | Q24676061 | ||
| HrpI of Erwinia amylovora functions in secretion of harpin and is a member of a new protein family | Q24681626 | ||
| HrpXv, an AraC-type regulator, activates expression of five of the six loci in the hrp cluster of Xanthomonas campestris pv. vesicatoria | Q24683344 | ||
| Flagellar switch of Salmonella typhimurium: gene sequences and deduced protein sequences | Q24684074 | ||
| Basic local alignment search tool | Q25938991 | ||
| The protein kinase family: conserved features and deduced phylogeny of the catalytic domains | Q27860528 | ||
| Integrins: versatility, modulation, and signaling in cell adhesion | Q27860844 | ||
| Plasmids of human strains of Yersinia enterocolitica: molecular relatedness and possible importance for pathogenesis | Q41531839 | ||
| Signal transduction between enteropathogenic Escherichia coli (EPEC) and epithelial cells: EPEC induces tyrosine phosphorylation of host cell proteins to initiate cytoskeletal rearrangement and bacterial uptake | Q41533005 | ||
| Essential virulence determinants of different Yersinia species are carried on a common plasmid | Q41536518 | ||
| Plasmid-mediated tissue invasiveness in Yersinia enterocolitica | Q41540478 | ||
| BIOSYNTHESIS AND PURIFICATION OF V AND W ANTIGEN IN PASTEURELLA PESTIS | Q41564589 | ||
| The record of horizontal gene transfer in Salmonella | Q41570645 | ||
| Molecular intimacy between proteins specifying plant-pathogen recognition | Q41576474 | ||
| Attachment and penetration of Escherichia coli into intestinal epithelium of the ileum in newborn pigs | Q41577121 | ||
| Morphological and cytoskeletal changes in epithelial cells occur immediately upon interaction with Salmonella typhimurium grown under low-oxygen conditions | Q41596545 | ||
| Identification of Salmonella typhimurium invasiveness loci | Q41610517 | ||
| Shigella flexneri induces apoptosis in infected macrophages | Q41614246 | ||
| Cytoskeletal rearrangements accompanying salmonella entry into epithelial cells | Q41681389 | ||
| Temperature-regulated expression of invasion genes inShigella flexneriis controlled through the transcriptional activation of thevirBgene on the large plasmid | Q41689426 | ||
| The specificity of carboxyl group modification during the inactivation of the Escherichia coli F1-ATPase with dicyclohexyl[14C]carbodiimide | Q42243990 | ||
| M ring, S ring and proximal rod of the flagellar basal body of Salmonella typhimurium are composed of subunits of a single protein, FliF. | Q42455767 | ||
| Additional structures associated with bacterial flagellar basal body | Q42481050 | ||
| Structural effects of mutations in Salmonella typhimurium flagellar switch complex | Q42481939 | ||
| Information essential for cell-cycle-dependent secretion of the 591-residue Caulobacter hook protein is confined to a 21-amino-acid sequence near the N-terminus | Q42488271 | ||
| Domain structures of the MS ring component protein (FliF) of the flagellar basal body of Salmonella typhimurium. | Q42498060 | ||
| Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator. | Q42502618 | ||
| FliN is a major structural protein of the C-ring in the Salmonella typhimurium flagellar basal body | Q42521620 | ||
| Cytopathogenic effect of Salmonella typhi GIFU 10007 on M cells of murine ileal Peyer's patches in ligated ileal loops: an ultrastructural study | Q42522319 | ||
| Role of hns in the virulence phenotype of pathogenic salmonellae | Q42595438 | ||
| Characterization of the hrpJ and hrpU operons of Pseudomonas syringae pv. syringae Pss61: similarity with components of enteric bacteria involved in flagellar biogenesis and demonstration of their role in HarpinPss secretion | Q42600314 | ||
| Cloning the structural gene for the 49-kDa form of exoenzyme S (exoS) from Pseudomonas aeruginosa strain 388. | Q42603935 | ||
| Temperature regulation of Shigella virulence: identification of the repressor gene virR, an analogue of hns, and partial complementation by tyrosyl transfer RNA (tRNA1(Tyr)) | Q42604044 | ||
| Identification and characterization of FliY, a novel component of the Bacillus subtilis flagellar switch complex | Q42605493 | ||
| icsB: a Shigella flexneri virulence gene necessary for the lysis of protrusions during intercellular spread | Q42607219 | ||
| Molecular cloning and characterization of a sym plasmid locus that regulates cultivar-specific nodulation of soybean by Rhizobium fredii USDA257. | Q42617995 | ||
| Erwinia stewartii WtsA, a positive regulator of pathogenicity gene expression, is similar to Pseudomonas syringae pv. phaseolicola HrpS. | Q42618042 | ||
| Modulation of bacterial entry into epithelial cells by association between vinculin and the Shigella IpaA invasin. | Q42618086 | ||
| EspA, a protein secreted by enteropathogenic Escherichia coli, is required to induce signals in epithelial cells. | Q42635284 | ||
| hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes | Q42638991 | ||
| Cloning and characterization of bfpTVW, genes required for the transcriptional activation of bfpA in enteropathogenic Escherichia coli | Q42642091 | ||
| Functional organization and nucleotide sequence of virulence Region-2 on the large virulence plasmid in Shigella flexneri 2a. | Q42642226 | ||
| The locus of enterocyte effacement pathogenicity island of enteropathogenic Escherichia coli encodes secretion functions and remnants of transposons at its extreme right end. | Q42649057 | ||
| Suppression of cytokines in mice by protein A-V antigen fusion peptide and restoration of synthesis by active immunization. | Q35429159 | ||
| Increased protein secretion and adherence to HeLa cells by Shigella spp. following growth in the presence of bile salts | Q35439004 | ||
| Spacious phagosome formation within mouse macrophages correlates with Salmonella serotype pathogenicity and host susceptibility | Q35451012 | ||
| Differential secretion of interleukin-8 by human epithelial cell lines upon entry of virulent or nonvirulent Yersinia enterocolitica. | Q35497441 | ||
| Infection of rabbit Peyer's patches by Shigella flexneri: effect of adhesive or invasive bacterial phenotypes on follicle-associated epithelium | Q35506252 | ||
| V antigen-polyhistidine fusion peptide: binding to LcrH and active immunity against plague | Q35526160 | ||
| The gene slyA of Salmonella typhimurium is required for destruction of M cells and intracellular survival but not for invasion or colonization of the murine small intestine | Q35531570 | ||
| In vivo apoptosis in Shigella flexneri infections | Q35532651 | ||
| Shigella flexneri is trapped in polymorphonuclear leukocyte vacuoles and efficiently killed | Q35533491 | ||
| Naturally occurring deletions in the centisome 63 pathogenicity island of environmental isolates of Salmonella spp | Q35545183 | ||
| A third secreted protein that is encoded by the enteropathogenic Escherichia coli pathogenicity island is required for transduction of signals and for attaching and effacing activities in host cells | Q35549056 | ||
| Synergistic effect of mutations in invA and lpfC on the ability of Salmonella typhimurium to cause murine typhoid. | Q35549256 | ||
| IpaB, a Shigella flexneri invasin, colocalizes with interleukin-1 beta-converting enzyme in the cytoplasm of macrophages | Q35567691 | ||
| Transcriptional analysis of the Pseudomonas aeruginosa exoenzyme S structural gene | Q35580149 | ||
| Mutations in yscC, yscD, and yscG prevent high-level expression and secretion of V antigen and Yops in Yersinia pestis | Q35589513 | ||
| Homologs of the Shigella IpaB and IpaC invasins are required for Salmonella typhimurium entry into cultured epithelial cells | Q35589961 | ||
| VirG, a Yersinia enterocolitica lipoprotein involved in Ca2+ dependency, is related to exsB of Pseudomonas aeruginosa | Q35590983 | ||
| Involvement of cpxA, a sensor of a two-component regulatory system, in the pH-dependent regulation of expression of Shigella sonnei virF gene | Q35593700 | ||
| Identification of two targets of the type III protein secretion system encoded by the inv and spa loci of Salmonella typhimurium that have homology to the Shigella IpaD and IpaA proteins | Q35599750 | ||
| Expression and localization of HrpA1, a protein of Xanthomonas campestris pv. vesicatoria essential for pathogenicity and induction ofthe hypersensitive reaction | Q35602596 | ||
| Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp. | Q35604121 | ||
| Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent | Q35617117 | ||
| Delineation and mutational analysis of the Yersinia pseudotuberculosis YopE domains which mediate translocation across bacterial and eukaryotic cellular membranes | Q35618079 | ||
| Analysis of the boundaries of Salmonella pathogenicity island 2 and the corresponding chromosomal region of Escherichia coli K-12. | Q35619848 | ||
| Yersinia pestis LcrV forms a stable complex with LcrG and may have a secretion-related regulatory role in the low-Ca2+ response | Q35620091 | ||
| Altered localization of HrpZ in Pseudomonas syringae pv. syringae hrp mutants suggests that different components of the type III secretion pathway control protein translocation across the inner and outer membranes of gram-negative bacteria | Q35624414 | ||
| Identification of type III secreted products of the Pseudomonas aeruginosa exoenzyme S regulon | Q35632593 | ||
| Analysis of the Streptomyces coelicolor sigE gene reveals the existence of a subfamily of eubacterial RNA polymerase sigma factors involved in the regulation of extracytoplasmic functions | Q35648817 | ||
| Genetics and biogenesis of bacterial flagella | Q35656714 | ||
| Construction and characterization of chromosomal insertional mutations of the Pseudomonas aeruginosa exoenzyme S trans-regulatory locus. | Q35773216 | ||
| Individual chaperones required for Yop secretion by Yersinia | Q35858391 | ||
| The yopM gene of Yersinia pestis encodes a released protein having homology with the human platelet surface protein GPIb alpha | Q35879197 | ||
| Status of YopM and YopN in the Yersinia Yop virulon: YopM of Y.enterocolitica is internalized inside the cytosol of PU5-1.8 macrophages by the YopB, D, N delivery apparatus | Q35909616 | ||
| Signaling in plant-microbe interactions | Q28235774 | ||
| The PTPase YopH inhibits uptake of Yersinia, tyrosine phosphorylation of p130Cas and FAK, and the associated accumulation of these proteins in peripheral focal adhesions | Q28239729 | ||
| Histone-like protein H1 (H-NS), DNA supercoiling, and gene expression in bacteria | Q28242053 | ||
| DNA supercoiling and environmental regulation of virulence gene expression in Shigella flexneri | Q28245605 | ||
| ymoA, a Yersinia enterocolitica chromosomal gene modulating the expression of virulence functions | Q28250224 | ||
| IpaB mediates macrophage apoptosis induced by Shigella flexneri | Q28254424 | ||
| Identification of a ten-amino acid proline-rich SH3 binding site | Q28266446 | ||
| Membrane traffic wardens and protein secretion in gram-negative bacteria | Q28266467 | ||
| A secreted protein kinase of Yersinia pseudotuberculosis is an indispensable virulence determinant | Q28266681 | ||
| Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg | Q28269092 | ||
| A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli | Q28280711 | ||
| The Yersinia YpkA Ser/Thr kinase is translocated and subsequently targeted to the inner surface of the HeLa cell plasma membrane | Q28286030 | ||
| Sequence and domain structure of talin | Q28302349 | ||
| Pathogenicity islands of virulent bacteria: structure, function and impact on microbial evolution | Q28307679 | ||
| Characterization of pilQ, a new gene required for the biogenesis of type 4 fimbriae in Pseudomonas aeruginosa | Q28492632 | ||
| Exoenzyme S of Pseudomonas aeruginosa is secreted by a type III pathway | Q28492720 | ||
| Analyses of the DNA-binding and transcriptional activation properties of ExsA, the transcriptional activator of the Pseudomonas aeruginosa exoenzyme S regulon | Q28492840 | ||
| Cloning and sequence analysis of a trans-regulatory locus required for exoenzyme S synthesis in Pseudomonas aeruginosa | Q28492993 | ||
| A bacterial invasin induces macrophage apoptosis by binding directly to ICE | Q28512900 | ||
| A nuclear pore complex protein that contains zinc finger motifs, binds DNA, and faces the nucleoplasm | Q28582932 | ||
| Protein secretion by enteropathogenic Escherichia coli is essential for transducing signals to epithelial cells | Q28776036 | ||
| Molecular basis of symbiosis between Rhizobium and legumes | Q29393489 | ||
| Integrins and signal transduction pathways: the road taken | Q29547895 | ||
| The complete general secretory pathway in gram-negative bacteria | Q29615298 | ||
| A proline-rich protein, verprolin, involved in cytoskeletal organization and cellular growth in the yeast Saccharomyces cerevisiae | Q30194734 | ||
| Yersinia pestis YopM: thrombin binding and overexpression | Q30451223 | ||
| Cloning and characterization of pathogenicity genes from Xanthomonas campestris pv. glycines | Q30982677 | ||
| Surface presentation of Shigella flexneri invasion plasmid antigens requires the products of the spa locus | Q30982682 | ||
| The Yersinia yop regulon | Q31052468 | ||
| Salmonella typhimurium mutants defective in flagellar filament regrowth and sequence similarity of FliI to F0F1, vacuolar, and archaebacterial ATPase subunits | Q33233253 | ||
| Sequence and molecular characterization of a multicopy invasion plasmid antigen gene, ipaH, of Shigella flexneri | Q33253819 | ||
| The secreted Ipa complex of Shigella flexneri promotes entry into mammalian cells | Q33552436 | ||
| Identification of a chromosomal gene controlling temperature-regulated expression of Shigella virulence | Q33568042 | ||
| Characterization of the Shigella flexneri ipgD and ipgF genes, which are located in the proximal part of the mxi locus | Q33594863 | ||
| Bacillus subtilis FlhA: a flagellar protein related to a new family of signal-transducing receptors | Q36741270 | ||
| Avirulence gene avrRxv from Xanthomonas campestris pv. vesicatoria specifies resistance on tomato line Hawaii 7998. | Q36759211 | ||
| SycE, a chaperone-like protein of Yersinia enterocolitica involved in Ohe secretion of YopE. | Q36783256 | ||
| Insertion of an outer membrane protein in Escherichia coli requires a chaperone-like protein. | Q36796337 | ||
| Yersinia enterocolitica induces apoptosis in macrophages by a process requiring functional type III secretion and translocation mechanisms and involving YopP, presumably acting as an effector protein | Q36827596 | ||
| Identification of a Salmonella typhimurium invasion locus by selection for hyperinvasive mutants | Q36864089 | ||
| Cytoskeletal composition of attaching and effacing lesions associated with enteropathogenic Escherichia coli adherence to HeLa cells | Q36946588 | ||
| Nucleotide sequence and transcriptional regulation of a positive regulatory gene of Shigella dysenteriae. | Q36956542 | ||
| Elevation of intracellular free calcium levels in HEp-2 cells infected with enteropathogenic Escherichia coli | Q36962955 | ||
| Two novel virulence loci, mxiA and mxiB, in Shigella flexneri 2a facilitate excretion of invasion plasmid antigens | Q36964736 | ||
| Distribution of the invA, -B, -C, and -D genes of Salmonella typhimurium among other Salmonella serovars: invA mutants of Salmonella typhi are deficient for entry into mammalian cells | Q36967459 | ||
| Humoral and cellular defense against intestinal murine infection with Yersinia enterocolitica | Q36974797 | ||
| Electron microscopic evidence for in vivo extracellular localization of Yersinia pseudotuberculosis harboring the pYV plasmid | Q36978722 | ||
| Construction and analysis of TnphoA mutants of enteropathogenic Escherichia coli unable to invade HEp-2 cells | Q36982240 | ||
| Expression of Salmonella typhimurium genes required for invasion is regulated by changes in DNA supercoiling | Q36984314 | ||
| Anaerobiosis, type 1 fimbriae, and growth phase are factors that affect invasion of HEp-2 cells by Salmonella typhimurium | Q36985210 | ||
| Plasmid and chromosomal elements involved in the pathogenesis of attaching and effacing Escherichia coli | Q36988590 | ||
| Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector | Q36989608 | ||
| Intracellular targeting of the Yersinia YopE cytotoxin in mammalian cells induces actin microfilament disruption | Q36990392 | ||
| Identification and mapping of the temperature-inducible, plasmid-encoded proteins of Yersinia spp | Q36993448 | ||
| Inhibition of phagocytosis in Yersinia pseudotuberculosis: a virulence plasmid-encoded ability involving the Yop2b protein | Q36998408 | ||
| Genetic analysis of the 9.5-kilobase virulence plasmid of Yersinia pestis. | Q37000237 | ||
| Plasminogen activator/coagulase gene of Yersinia pestis is responsible for degradation of plasmid-encoded outer membrane proteins | Q37000247 | ||
| Serum immune response to Shigella protein antigens in rhesus monkeys and humans infected with Shigella spp | Q37010733 | ||
| Isolation, characterization, and mapping of Tn5 insertions into the 140-megadalton invasion plasmid defective in the mouse Sereny test in Shigella flexneri 2a | Q37011844 | ||
| A low-Ca2+ response operon encodes the V antigen of Yersinia pestis. | Q37013218 | ||
| Identification of Shigella invasion genes by isolation of temperature-regulated inv::lacZ operon fusions | Q37024672 | ||
| Identification and antigenic characterization of virulence-associated, plasmid-coded proteins of Shigella spp. and enteroinvasive Escherichia coli | Q37031232 | ||
| Immune response to plasmid- and chromosome-encoded Yersinia antigens | Q37033115 | ||
| Expression of the temperature-inducible outer membrane proteins of yersiniae. | Q37048498 | ||
| Transfer of the virulence plasmid of Yersinia pestis to Yersinia pseudotuberculosis | Q37048515 | ||
| Cloning of plasmid DNA sequences involved in invasion of HeLa cells by Shigella flexneri | Q37051175 | ||
| Multiplication of Shigella flexneri within HeLa cells: lysis of the phagocytic vacuole and plasmid-mediated contact hemolysis | Q37056339 | ||
| Molecular and functional characterization of the Salmonella typhimurium invasion genes invB and invC: homology of InvC to the F0F1 ATPase family of proteins | Q35967361 | ||
| YscU, a Yersinia enterocolitica inner membrane protein involved in Yop secretion | Q35967399 | ||
| Electron microscope studies of experimental Salmonella infection. I. Penetration into the intestinal epithelium by Salmonella typhimurium | Q35972318 | ||
| Co-ordinate expression of virulence genes by ToxR in Vibrio cholerae | Q35988328 | ||
| Exerimental acute colitis in the Rhesus monkey following peroral infection with Shigella flexneri. An electron microscope study | Q36051645 | ||
| Hrp pilus: an hrp-dependent bacterial surface appendage produced by Pseudomonas syringae pv. tomato DC3000 | Q36086934 | ||
| LcrG, a secreted protein involved in negative regulation of the low-calcium response in Yersinia pestis | Q36101650 | ||
| Analysis of the structure and subcellular location of filamentous phage pIV | Q36102328 | ||
| A PhoP-repressed gene promotes Salmonella typhimurium invasion of epithelial cells | Q36103190 | ||
| A second chromosomal gene necessary for intimate attachment of enteropathogenic Escherichia coli to epithelial cells. | Q36103634 | ||
| Molecular analysis of avirulence gene avrRpt2 and identification of a putative regulatory sequence common to all known Pseudomonas syringae avirulence genes | Q36103789 | ||
| Mutation of flgM attenuates virulence of Salmonella typhimurium, and mutation of fliA represses the attenuated phenotype | Q36104702 | ||
| A low-Ca2+ response (LCR) secretion (ysc) locus lies within the lcrB region of the LCR plasmid in Yersinia pestis | Q36104958 | ||
| YscN, the putative energizer of the Yersinia Yop secretion machinery | Q36105907 | ||
| Transcriptional organization of the trans-regulatory locus which controls exoenzyme S synthesis in Pseudomonas aeruginosa | Q36108615 | ||
| Identification of DNA sequences recognized by VirF, the transcriptional activator of the Yersinia yop regulon | Q36108647 | ||
| Organization and environmental regulation of the Pseudomonas syringae pv. syringae 61 hrp cluster | Q36110044 | ||
| Phenotypic expression of the Pseudomonas syringae pv. syringae 61 hrp/hrm gene cluster in Escherichia coli MC4100 requires a functional porin | Q36110053 | ||
| Expression of Erwinia amylovora hrp genes in response to environmental stimuli | Q36110192 | ||
| A novel protein, LcrQ, involved in the low-calcium response of Yersinia pseudotuberculosis shows extensive homology to YopH | Q36111695 | ||
| Plant and environmental sensory signals control the expression of hrp genes in Pseudomonas syringae pv. phaseolicola | Q36111895 | ||
| Identification of novel loci affecting entry of Salmonella enteritidis into eukaryotic cells | Q36112510 | ||
| Nucleotide sequences of Bacillus subtilis flagellar biosynthetic genes fliP and fliQ and identification of a novel flagellar gene, fliZ | Q36112588 | ||
| Temperature sensing in Yersinia pestis: regulation of yopE transcription by lcrF | Q36113530 | ||
| Molecular and functional characterization of the Salmonella invasion gene invA: homology of InvA to members of a new protein family | Q36113628 | ||
| Structure and regulation of the Yersinia pestis yscBCDEF operon | Q36114525 | ||
| Nonpolar mutagenesis of the ipa genes defines IpaB, IpaC, and IpaD as effectors of Shigella flexneri entry into epithelial cells | Q36122200 | ||
| Genetic and transcriptional organization of the hrp cluster of Pseudomonas syringae pv. phaseolicola | Q36125492 | ||
| Analysis of the V antigen lcrGVH-yopBD operon of Yersinia pseudotuberculosis: evidence for a regulatory role of LcrH and LcrV. | Q36131333 | ||
| Secretion of hybrid proteins by the Yersinia Yop export system | Q36131436 | ||
| The Pseudomonas syringae pv. syringae 61 hrpH product, an envelope protein required for elicitation of the hypersensitive response in plants | Q36132365 | ||
| The Yersinia pestis V antigen is a regulatory protein necessary for Ca2(+)-dependent growth and maximal expression of low-Ca2+ response virulence genes | Q36144953 | ||
| The flaA locus of Bacillus subtilis is part of a large operon coding for flagellar structures, motility functions, and an ATPase-like polypeptide | Q36146762 | ||
| Genetic analysis of an invasion region by use of a Tn3-lac transposon and identification of a second positive regulator gene, invE, for cell invasion of Shigella sonnei: significant homology of invE with ParB of plasmid P1 | Q36157790 | ||
| Interaction of chlamydiae and host cells in vitro | Q37056842 | ||
| Distinctive patterns of adherence of enteropathogenic Escherichia coli to HeLa cells | Q37077312 | ||
| Characterization of common virulence plasmids in Yersinia species and their role in the expression of outer membrane proteins | Q37079843 | ||
| Molecular recognition of pathogen attack occurs inside of plant cells in plant disease resistance specified by the Arabidopsis genes RPS2 and RPM1. | Q37098663 | ||
| Attaching and effacing activities of rabbit and human enteropathogenic Escherichia coli in pig and rabbit intestines. | Q37106331 | ||
| Characterization of virulence plasmids and plasmid-associated outer membrane proteins in Shigella flexneri, Shigella sonnei, and Escherichia coli. | Q37111101 | ||
| Salmonella typhimurium invasion induces apoptosis in infected macrophages | Q37364881 | ||
| Tyrosine phosphate hydrolysis of host proteins by an essential Yersinia virulence determinant | Q37397346 | ||
| Identification of a pathogenicity island required for Salmonella survival in host cells | Q37441337 | ||
| Pseudomonas aeruginosa exoenzyme S: an adenosine diphosphate ribosyltransferase distinct from toxin A | Q37590200 | ||
| The two-component regulatory system ompR-envZ controls the virulence of Shigella flexneri | Q37608464 | ||
| Functional conservation of the secretion and translocation machinery for virulence proteins of yersiniae, salmonellae and shigellae. | Q37621979 | ||
| Identification of a virulence locus encoding a second type III secretion system in Salmonella typhimurium | Q37698755 | ||
| Pore-forming cytolysins of gram-negative bacteria | Q37750817 | ||
| Protein H1: a role for chromatin structure in the regulation of bacterial gene expression and virulence? | Q37834160 | ||
| Actin-membrane interaction in focal adhesions | Q37835360 | ||
| Type III secretion genes identify a putative virulence locus of Chlamydia | Q37882492 | ||
| Origins and functions of the chlamydial inclusion. | Q37882573 | ||
| Chlamydia psittaci IncA is phosphorylated by the host cell and is exposed on the cytoplasmic face of the developing inclusion | Q37883116 | ||
| Chlamydia trachomatis serovar L2 induces protein tyrosine phosphorylation during uptake by HeLa cells | Q37888188 | ||
| Mobilization of F-actin and clathrin during redistribution of Chlamydia trachomatis to an intracellular site in eucaryotic cells | Q37894141 | ||
| Altered pH and lysine signalling mutants of cadC, a gene encoding a membrane-bound transcriptional activator of the Escherichia coli cadBA operon | Q38303972 | ||
| Transcriptional control of the invasion regulatory gene virB of Shigella flexneri: activation by virF and repression by H-NS. | Q38315694 | ||
| ATP synthesis by oxidative phosphorylation | Q39465606 | ||
| The plasmid-encoded outer-membrane proteins of Yersinia pestis | Q39538089 | ||
| Genetic determinants of Shigella pathogenicity | Q39548216 | ||
| Biogenesis of lipoproteins in bacteria. | Q39740997 | ||
| Yersinia enterocolitica, a primary model for bacterial invasiveness | Q39759560 | ||
| Yersinia pseudotuberculosis inhibits Fc receptor-mediated phagocytosis in J774 cells | Q39822718 | ||
| Expression of attaching/effacing activity by enteropathogenic Escherichia coli depends on growth phase, temperature, and protein synthesis upon contact with epithelial cells. | Q39824424 | ||
| Soluble invasion plasmid antigen C (IpaC) from Shigella flexneri elicits epithelial cell responses related to pathogen invasion | Q39826253 | ||
| Intimin-dependent binding of enteropathogenic Escherichia coli to host cells triggers novel signaling events, including tyrosine phosphorylation of phospholipase C-gamma1. | Q39830271 | ||
| Enteropathogenic Escherichia coli protein secretion is induced in response to conditions similar to those in the gastrointestinal tract. | Q39830323 | ||
| Secretion of Shigella flexneri Ipa invasins on contact with epithelial cells and subsequent entry of the bacterium into cells are growth stage dependent | Q39833319 | ||
| Thermoregulation of virB transcription in Shigella flexneri by sensing of changes in local DNA superhelicity | Q39835748 | ||
| hrpL activates Erwinia amylovora hrp gene transcription and is a member of the ECF subfamily of sigma factors | Q39838950 | ||
| Random and directed mutagenesis to elucidate the functional importance of helix II and F-989 in the C-terminal secretion signal of Escherichia coli hemolysin | Q39840412 | ||
| Mutations in fliK and flhB affecting flagellar hook and filament assembly in Salmonella typhimurium | Q39841418 | ||
| The Pseudomonas syringae Hrp regulation and secretion system controls the production and secretion of multiple extracellular proteins | Q39843369 | ||
| Assembly of the switch complex onto the MS ring complex of Salmonella typhimurium does not require any other flagellar proteins | Q39844258 | ||
| Flagellar assembly in Salmonella typhimurium: analysis with temperature-sensitive mutants | Q36159115 | ||
| Constitutive expression of the phoP regulon attenuates Salmonella virulence and survival within macrophages | Q36162205 | ||
| Expression of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria is not under the control of hrp genes and is independent of plant factors | Q36165893 | ||
| LcrD, a membrane-bound regulator of the Yersinia pestis low-calcium response | Q36166049 | ||
| The eukaryotic host factor that activates exoenzyme S of Pseudomonas aeruginosa is a member of the 14-3-3 protein family | Q36167740 | ||
| Homology between virF, the transcriptional activator of the Yersinia virulence regulon, and AraC, the Escherichia coli arabinose operon regulator | Q36173040 | ||
| L-, P-, and M-ring proteins of the flagellar basal body of Salmonella typhimurium: gene sequences and deduced protein sequences | Q36179875 | ||
| The predicted protein product of a pathogenicity locus from Pseudomonas syringae pv. phaseolicola is homologous to a highly conserved domain of several procaryotic regulatory proteins | Q36181850 | ||
| Molecular analysis of lcrGVH, the V antigen operon of Yersinia pestis | Q36182922 | ||
| Molecular cloning of a Pseudomonas syringae pv. syringae gene cluster that enables Pseudomonas fluorescens to elicit the hypersensitive response in tobacco plants | Q36219048 | ||
| The Yersinia tyrosine phosphatase: specificity of a bacterial virulence determinant for phosphoproteins in the J774A.1 macrophage | Q36232127 | ||
| Molecular cloning of invasion plasmid antigen (ipa) genes from Shigella flexneri: analysis of ipa gene products and genetic mapping | Q36238161 | ||
| lcrR, a low-Ca2(+)-response locus with dual Ca2(+)-dependent functions in Yersinia pestis | Q36256151 | ||
| Gene cluster of Pseudomonas syringae pv. "phaseolicola" controls pathogenicity of bean plants and hypersensitivity of nonhost plants | Q36259921 | ||
| The route of enteric infection in normal mice | Q36273394 | ||
| Pseudomonas solanacearum genes controlling both pathogenicity on tomato and hypersensitivity on tobacco are clustered | Q36274769 | ||
| Modular arrangement of proteins as inferred from analysis of homology. | Q36278463 | ||
| Isolation and characterization of Ca2+-blind mutants of Yersinia pestis | Q36279082 | ||
| Temperature-controlled plasmid regulon associated with low calcium response in Yersinia pestis | Q36281599 | ||
| Sequence of the flaA (cheC) locus of Escherichia coli and discovery of a new gene | Q36296969 | ||
| Genetic analysis of the low calcium response in Yersinia pestis mu d1(Ap lac) insertion mutants | Q36304161 | ||
| Consequences of Ca2+ deficiency on macromolecular synthesis and adenylate energy charge in Yersinia pestis | Q36334014 | ||
| Alterations in the pathogenicity of Escherichia coli K-12 after transfer of plasmid and chromosomal genes from Shigella flexneri | Q36347107 | ||
| Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer's patches. | Q36363455 | ||
| Acute inflammation causes epithelial invasion and mucosal destruction in experimental shigellosis | Q36363758 | ||
| Cytoskeletal rearrangements and the functional role of T-plastin during entry of Shigella flexneri into HeLa cells | Q36382504 | ||
| Shigella sonnei plasmids: evidence that a large plasmid is necessary for virulence. | Q36428530 | ||
| Involvement of a plasmid in the invasive ability of Shigella flexneri. | Q36437346 | ||
| Plasmids in Yersinia pestis. | Q36443764 | ||
| A secreted Salmonella protein with homology to an avirulence determinant of plant pathogenic bacteria. | Q36578118 | ||
| Cloning and characterization of a Chlamydia psittaci gene coding for a protein localized in the inclusion membrane of infected cells. | Q36707897 | ||
| A 40 kb chromosomal fragment encoding Salmonella typhimurium invasion genes is absent from the corresponding region of the Escherichia coli K-12 chromosome | Q36707901 | ||
| Map-based cloning of a protein kinase gene conferring disease resistance in tomato | Q36721116 | ||
| Enteropathogenic Escherichia coli of classic serotypes associated with infant diarrhea: epidemiology and pathogenesis | Q40189710 | ||
| Infections caused by Pseudomonas aeruginosa | Q40207100 | ||
| EPITHELIAL CELL PENETRATION AS AN ESSENTIAL STEP IN THE PATHOGENESIS OF BACILLARY DYSENTERY. | Q40250130 | ||
| Yops of Yersinia spp. pathogenic for humans. | Q40268028 | ||
| The basis of virulence in Pasteurella pestis: an antigen determining virulence | Q40293937 | ||
| Role of calcium ions in the stimulation of growth of virulent strains of Pasteurella pestis | Q40314716 | ||
| Studies on the nutrition and physiology of Pasteurella pestis. III. Effects of calcium ions on the growth of virulent and avirulent strains of Pasteurella pestis. | Q40315905 | ||
| YopB and YopD constitute a novel class of Yersinia Yop proteins. | Q40373613 | ||
| The XylS/AraC family of regulators. | Q40405372 | ||
| Role of M cells in initial antigen uptake and in ulcer formation in the rabbit intestinal loop model of shigellosis | Q40426449 | ||
| Actin accumulation at sites of bacterial adhesion to tissue culture cells: basis of a new diagnostic test for enteropathogenic and enterohemorrhagic Escherichia coli | Q40426825 | ||
| Secretion of Yop proteins by Yersiniae | Q40428310 | ||
| Moving through the membrane with filamentous phages. | Q40466973 | ||
| Molecular genetics of plant disease resistance | Q40514697 | ||
| Nucleotide sequence of invasion plasmid antigen gene ipaA from Shigella flexneri 5. | Q40515337 | ||
| Erwinia chrysanthemi and Pseudomonas syringae: plant pathogens trafficking in extracellular virulence proteins. | Q40595522 | ||
| hrp genes of phytopathogenic bacteria | Q40595526 | ||
| High-molecular-weight plasmid correlates with Escherichia coli enteroinvasiveness | Q40598653 | ||
| Common components in the assembly of type 4 fimbriae, DNA transfer systems, filamentous phage and protein-secretion apparatus: a general system for the formation of surface-associated protein complexes | Q40637003 | ||
| Non-invasive Salmonella typhimurium mutants are avirulent because of an inability to enter and destroy M cells of ileal Peyer's patches | Q40651358 | ||
| Simultaneous identification of bacterial virulence genes by negative selection. | Q40682435 | ||
| Typhoid fever and other salmonellosis: a continuing challenge | Q40683373 | ||
| Adaptation of a conjugal transfer system for the export of pathogenic macromolecules | Q40721209 | ||
| Conservation of secretion pathways for pathogenicity determinants of plant and animal bacteria | Q40733114 | ||
| Microbial recognition and activation of plant defense systems | Q40733122 | ||
| PopA1, a protein which induces a hypersensitivity-like response on specific Petunia genotypes, is secreted via the Hrp pathway of Pseudomonas solanacearum. | Q40790729 | ||
| Target cell contact triggers expression and polarized transfer of Yersinia YopE cytotoxin into mammalian cells. | Q40790987 | ||
| The secretion of the Shigella flexneri Ipa invasins is activated by epithelial cells and controlled by IpaB and IpaD. | Q40793797 | ||
| Contact of Shigella with host cells triggers release of Ipa invasins and is an essential function of invasiveness | Q40806867 | ||
| Invasion of epithelial cells by Shigella flexneri induces tyrosine phosphorylation of cortactin by a pp60c-src-mediated signalling pathway | Q40806872 | ||
| Plant disease resistance genes in signal perception and transduction | Q40816982 | ||
| Regulation by Ca2+ in the Yersinia low-Ca2+ response | Q40840513 | ||
| Cognate gene clusters govern invasion of host epithelial cells by Salmonella typhimurium and Shigella flexneri | Q40874006 | ||
| Strategies for development of potential candidate Shigella vaccines | Q40879028 | ||
| Customized secretion chaperones in pathogenic bacteria | Q41057356 | ||
| Invasion and the pathogenesis of Shigella infections | Q41064944 | ||
| A pathogenic bacterium triggers epithelial signals to form a functional bacterial receptor that mediates actin pseudopod formation. | Q41065159 | ||
| Rho-dependent membrane folding causes Shigella entry into epithelial cells | Q41075099 | ||
| The YopB protein of Yersinia pseudotuberculosis is essential for the translocation of Yop effector proteins across the target cell plasma membrane and displays a contact-dependent membrane disrupting activity | Q41077827 | ||
| ExoU expression by Pseudomonas aeruginosa correlates with acute cytotoxicity and epithelial injury | Q41095866 | ||
| Bacterial entry into epithelial cells: the paradigm of Shigella | Q41104097 | ||
| Identification of Pseudomonas aeruginosa genes required for epithelial cell injury | Q41106969 | ||
| Role of the transcriptional activator, VirF, and temperature in the expression of the pYV plasmid genes of Yersinia enterocolitica | Q41114516 | ||
| YopK of Yersinia pseudotuberculosis controls translocation of Yop effectors across the eukaryotic cell membrane | Q41118367 | ||
| Flagellar assembly in Salmonella typhimurium | Q41121961 | ||
| M cells and the pathogenesis of mucosal and systemic infections | Q41125667 | ||
| Plasmid associated with pathogenicity and calcium dependency of Yersinia enterocolitica | Q41157319 | ||
| Presence of a virulence-associated plasmid in Yersinia pseudotuberculosis | Q41170748 | ||
| A secreted protein tyrosine phosphatase with modular effector domains in the bacterial pathogen Salmonella typhimurium | Q41178388 | ||
| YopH of Yersinia pseudotuberculosis interrupts early phosphotyrosine signalling associated with phagocytosis | Q41193873 | ||
| Identification of a novel virulence gene, virA, on the large plasmid of Shigella, involved in invasion and intercellular spreading | Q41333107 | ||
| Functional analysis of the Salmonella typhimurium invasion genes invl and invJ and identification of a target of the protein secretion apparatus encoded in the inv locus | Q41394091 | ||
| Interactions between enteropathogenic Escherichia coli and host epithelial cells. | Q41395888 | ||
| Contact with eukaryotic cells: a new signal triggering bacterial gene expression | Q41435436 | ||
| Molecular and cellular mechanisms of tissue invasion by Shigella flexneri | Q41448226 | ||
| Type III secretion systems: machines to deliver bacterial proteins into eukaryotic cells? | Q41462606 | ||
| A diarrheal pathogen, enteropathogenic Escherichia coli (EPEC), triggers a flux of inositol phosphates in infected epithelial cells | Q41483810 | ||
| Contact with epithelial cells induces the formation of surface appendages on Salmonella typhimurium | Q41486433 | ||
| YscM1 and YscM2, two Yersinia enterocolitica proteins causing downregulation of yop transcription. | Q41487121 | ||
| The exoenzyme S regulon of Pseudomonas aeruginosa | Q41487139 | ||
| A mRNA signal for the type III secretion of Yop proteins by Yersinia enterocolitica | Q41487461 | ||
| Intracellular targeting of exoenzyme S of Pseudomonas aeruginosa via type III-dependent translocation induces phagocytosis resistance, cytotoxicity and disruption of actin microfilaments | Q41487515 | ||
| Two independent type III secretion mechanisms for YopE in Yersinia enterocolitica | Q41488408 | ||
| Functional analysis of ssaJ and the ssaK/U operon, 13 genes encoding components of the type III secretion apparatus of Salmonella Pathogenicity Island 2. | Q41488627 | ||
| Modulation of virulence factor expression by pathogen target cell contact | Q41490662 | ||
| The cytosolic SycE and SycH chaperones of Yersinia protect the region of YopE and YopH involved in translocation across eukaryotic cell membranes | Q41491050 | ||
| Interaction of Ipa proteins of Shigella flexneri with alpha5beta1 integrin promotes entry of the bacteria into mammalian cells | Q41491681 | ||
| Sequence and expression analysis of the hrpB pathogenicity operon of Xanthomonas campestris pv. vesicatoria which encodes eight proteins with similarity to components of the Hrp, Ysc, Spa, and Fli secretion systems | Q41493133 | ||
| Mutational analysis of the Yersinia enterocolitica virC operon: characterization of yscE, F, G, I, J, K required for Yop secretion and yscH encoding YopR. | Q41493350 | ||
| Cell-surface-bound Yersinia translocate the protein tyrosine phosphatase YopH by a polarized mechanism into the target cell | Q41493370 | ||
| The CompletehrpGene Cluster ofPseudomonas syringaepv.syringae61 Includes Two Blocks of Genes Required for HarpinPssSecretion that Are Arranged Colinearly withYersinia yscHomologs | Q41493738 | ||
| The HrpZ proteins of Pseudomonas syringae pvs. syringae, glycinea, and tomato are encoded by an operon containing Yersinia ysc homologs and elicit the hypersensitive response in tomato but not soybean. | Q41493747 | ||
| MxiG, a membrane protein required for secretion of Shigella spp. Ipa invasins: involvement in entry into epithelial cells and in intercellular dissemination | Q41493869 | ||
| PhoP/PhoQ transcriptional repression of Salmonella typhimurium invasion genes: evidence for a role in protein secretion. | Q41494361 | ||
| The chaperone-like protein YerA of Yersinia pseudotuberculosis stabilizes YopE in the cytoplasm but is dispensible for targeting to the secretion loci | Q41494795 | ||
| The hrp gene locus of Pseudomonas solanacearum, which controls the production of a type III secretion system, encodes eight proteins related to components of the bacterial flagellar biogenesis complex. | Q41495226 | ||
| Extracellular association and cytoplasmic partitioning of the IpaB and IpaC invasins of S. flexneri | Q41497452 | ||
| Translocation of a hybrid YopE-adenylate cyclase from Yersinia enterocolitica into HeLa cells | Q41497627 | ||
| Thermoregulation in Yersinia enterocolitica is coincident with changes in DNA supercoiling | Q41499692 | ||
| Characterization of the Pseudomonas syringae pv. syringae 61 hrpJ and hrpI genes: homology of HrpI to a superfamily of proteins associated with protein translocation | Q41502700 | ||
| MxiD, an outer membrane protein necessary for the secretion of the Shigella flexneri lpa invasins | Q41504166 | ||
| Cloning and molecular characterization of a gene involved in Salmonella adherence and invasion of cultured epithelial cells | Q41504292 | ||
| Expression, purification, and physicochemical characterization of a recombinant Yersinia protein tyrosine phosphatase | Q41504858 | ||
| A surface protease and the invasive character of plague | Q41504890 | ||
| Evidence that the hrpB gene encodes a positive regulator of pathogenicity genes from Pseudomonas solanacearum | Q41505154 | ||
| Determinants of pathogenicity in Xanthomonas campestris pv. vesicatoria are related to proteins involved in secretion in bacterial pathogens of animals | Q41505348 | ||
| hrp genes of Pseudomonas solanacearum are homologous to pathogenicity determinants of animal pathogenic bacteria and are conserved among plant pathogenic bacteria | Q41505355 | ||
| The surface-located YopN protein is involved in calcium signal transduction inYersinia pseudotuberculosis | Q41509042 | ||
| Protein tyrosine phosphatase activity of an essential virulence determinant in Yersinia | Q41511214 | ||
| The hrpA and hrpC operons of Erwinia amylovora encode components of a type III pathway that secretes harpin | Q39844794 | ||
| Comparative genetics of the inv-spa invasion gene complex of Salmonella enterica | Q39844957 | ||
| Excision of large DNA regions termed pathogenicity islands from tRNA-specific loci in the chromosome of an Escherichia coli wild-type pathogen. | Q39859232 | ||
| Characterization of the operon encoding the YpkA Ser/Thr protein kinase and the YopJ protein of Yersinia pseudotuberculosis | Q39896187 | ||
| Roles of FliK and FlhB in determination of flagellar hook length in Salmonella typhimurium | Q39897839 | ||
| Isolation and characterization of FliK-independent flagellation mutants from Salmonella typhimurium | Q39899605 | ||
| Molecular characterization of the Salmonella typhimurium flhB operon and its protein products | Q39899611 | ||
| Eight genes in region 5 that form an operon are essential for invasion of epithelial cells by Shigella flexneri 2a | Q39928014 | ||
| Multiple effects of lcrD mutations in Yersinia pestis | Q39928953 | ||
| Molecular characterization, nucleotide sequence, and expression of the fliO, fliP, fliQ, and fliR genes of Escherichia coli | Q39930043 | ||
| Identification of a putative alternate sigma factor and characterization of a multicomponent regulatory cascade controlling the expression of Pseudomonas syringae pv. syringae Pss61 hrp and hrmA genes | Q39930590 | ||
| The lcrB (yscN/U) gene cluster of Yersinia pseudotuberculosis is involved in Yop secretion and shows high homology to the spa gene clusters of Shigella flexneri and Salmonella typhimurium | Q39931711 | ||
| A single promoter sequence recognized by a newly identified alternate sigma factor directs expression of pathogenicity and host range determinants in Pseudomonas syringae | Q39931999 | ||
| A role for H-NS in the thermo-osmotic regulation of virulence gene expression in Shigella flexneri | Q39932607 | ||
| MxiJ, a lipoprotein involved in secretion of Shigella Ipa invasins, is homologous to YscJ, a secretion factor of the Yersinia Yop proteins | Q39939945 | ||
| Genetic analysis of the yopE region of Yersinia spp.: identification of a novel conserved locus, yerA, regulating yopE expression | Q39944282 | ||
| The lcrE gene is part of an operon in the lcr region of Yersinia enterocolitica O:3. | Q39945988 | ||
| DNA sequence analysis, gene product identification, and localization of flagellar motor components of Escherichia coli | Q39948911 | ||
| Virulence-associated genetic regions comprising 31 kilobases of the 230-kilobase plasmid in Shigella flexneri 2a. | Q39953337 | ||
| Large, unstable inserts in the chromosome affect virulence properties of uropathogenic Escherichia coli O6 strain 536. | Q39960997 | ||
| The UNC operon nucleotide sequence, regulation and structure of ATP-synthase | Q40111464 | ||
| mxiA of Shigella flexneri 2a, which facilitates export of invasion plasmid antigens, encodes a homolog of the low-calcium-response protein, LcrD, of Yersinia pestis | Q40147587 | ||
| Anaerobic growth of Salmonella typhimurium results in increased uptake by Henle 407 epithelial and mouse peritoneal cells in vitro and repression of a major outer membrane protein | Q40149767 | ||
| DNA sequence and product analysis of the virF locus responsible for congo red binding and cell invasion in Shigella flexneri 2a. | Q40161711 | ||
| Immunochemical analysis of plasmid-encoded proteins released by enteropathogenic Yersinia sp. grown in calcium-deficient media | Q40161831 | ||
| Genetically manipulated virulence of Yersinia enterocolitica. | Q40167837 | ||
| Expression of antigens encoded by the virulence plasmid of Yersinia enterocolitica under different growth conditions | Q40168144 | ||
| Identification of additional virulence determinants on the pYV plasmid of Yersinia enterocolitica W227 | Q35100760 | ||
| YopM inhibits platelet aggregation and is necessary for virulence of Yersinia pestis in mice | Q35105786 | ||
| Pseudomonas aeruginosa Exoenzyme S | Q35230168 | ||
| Environmental regulation of Shigella virulence | Q35231982 | ||
| Enteropathogenic Escherichia coli. | Q35381252 | ||
| Inhibition of the Fc receptor-mediated oxidative burst in macrophages by the Yersinia pseudotuberculosis tyrosine phosphatase. | Q35387662 | ||
| Functional conservation among members of the Salmonella typhimurium InvA family of proteins | Q35389195 | ||
| Bacterial evasion of host immune defense: Yersinia enterocolitica encodes a suppressor for tumor necrosis factor alpha expression. | Q35399143 | ||
| Characterization of Pseudomonas aeruginosa-induced MDCK cell injury: glycosylation-defective host cells are resistant to bacterial killing. | Q35404665 | ||
| A plasmid-encoded regulatory region activates chromosomal eaeA expression in enteropathogenic Escherichia coli. | Q35409065 | ||
| Virulence plasmid-encoded YopK is essential for Yersinia pseudotuberculosis to cause systemic infection in mice. | Q35417816 | ||
| Transepithelial signaling to neutrophils by salmonellae: a novel virulence mechanism for gastroenteritis. | Q35418436 | ||
| Active immunization with recombinant V antigen from Yersinia pestis protects mice against plague | Q35426559 | ||
| Cytoplasmic and membrane proteins of yersiniae cultivated under conditions simulating mammalian intracellular environment | Q35427286 | ||
| Pseudomonas aeruginosa exoenzyme S requires a eukaryotic protein for ADP-ribosyltransferase activity | Q67985296 | ||
| Transcriptional Organization and Expression of the LargehrpGene Cluster ofPseudomonas solanacearum | Q68181966 | ||
| Molecular characterization of a trans-acting, positive effector (ipaR) of invasion plasmid antigen synthesis in Shigella flexneri serotype 5 | Q68471375 | ||
| Localization of plasmid loci necessary for the entry of Shigella flexneri into HeLa cells, and characterization of one locus encoding four immunogenic polypeptides | Q69841428 | ||
| The role of exoenzyme S in infections with Pseudomonas aeruginosa | Q70101686 | ||
| Cytochalasins block actin filament elongation by binding to high affinity sites associated with F-actin | Q71138072 | ||
| The secretin-specific, chaperone-like protein of the general secretory pathway: separation of proteolytic protection and piloting functions | Q71911352 | ||
| Mutants at conserved positions in gene IV, a gene required for assembly and secretion of filamentous phages | Q72431336 | ||
| Coiled-coil domains in proteins secreted by type III secretion systems | Q73663925 | ||
| Identification and molecular characterization of a Salmonella typhimurium gene involved in triggering the internalization of salmonellae into cultured epithelial cells | Q33612050 | ||
| The lpf fimbrial operon mediates adhesion of Salmonella typhimurium to murine Peyer's patches | Q33616531 | ||
| The ability of Salmonella to enter mammalian cells is affected by bacterial growth state | Q33616743 | ||
| Identification of the YopE and YopH domains required for secretion and internalization into the cytosol of macrophages, using the cyaA gene fusion approach | Q33638561 | ||
| Characterization of invasion plasmid antigen genes (ipaBCD) from Shigella flexneri | Q33682684 | ||
| A genetic locus of enteropathogenic Escherichia coli necessary for the production of attaching and effacing lesions on tissue culture cells | Q33834748 | ||
| Identification of p130Cas as a substrate of Yersinia YopH (Yop51), a bacterial protein tyrosine phosphatase that translocates into mammalian cells and targets focal adhesions | Q33886658 | ||
| Enteropathogenic Escherichia coli contains a putative type III secretion system necessary for the export of proteins involved in attaching and effacing lesion formation | Q34022530 | ||
| Relationship between evolutionary rate and cellular location among the Inv/Spa invasion proteins of Salmonella enterica | Q34040164 | ||
| Effect of silica on the innate resistance of inbred mice to Salmonella typhimurium infection | Q34089517 | ||
| Polymorphonuclear leukocyte transmigration promotes invasion of colonic epithelial monolayer by Shigella flexneri | Q34125052 | ||
| Interleukin 1 is released by murine macrophages during apoptosis induced by Shigella flexneri | Q34186287 | ||
| The cytotoxic protein YopE of Yersinia obstructs the primary host defence | Q34215777 | ||
| Intestinal epithelial cell protein phosphorylation in enteropathogenic Escherichia coli diarrhoea | Q34242044 | ||
| Disulfide oxidoreductase activity of Shigella flexneri is required for release of Ipa proteins and invasion of epithelial cells | Q34275598 | ||
| Characterization of plasmids and plasmid-associated determinants of Yersinia enterocolitica pathogenesis | Q34281821 | ||
| Export of an N-terminal fragment of Escherichia coli flagellin by a flagellum-specific pathway | Q34285883 | ||
| A two-component regulatory system (phoP phoQ) controls Salmonella typhimurium virulence. | Q34286908 | ||
| Penetration of human intestinal epithelial cells by Salmonella: molecular cloning and expression of Salmonella typhi invasion determinants in Escherichia coli | Q34288319 | ||
| Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells | Q34298444 | ||
| HrpG, a key hrp regulatory protein of Xanthomonas campestris pv. vesicatoria is homologous to two-component response regulators. | Q34402712 | ||
| Association between virulence of Yersinia pestis and suppression of gamma interferon and tumor necrosis factor alpha. | Q34520336 | ||
| The eaeB gene of enteropathogenic Escherichia coli is necessary for signal transduction in epithelial cells | Q34531321 | ||
| Identification and characterization of a Salmonella typhimurium oxygen-regulated gene required for bacterial internalization. | Q34536508 | ||
| Passive immunity to yersiniae mediated by anti-recombinant V antigen and protein A-V antigen fusion peptide | Q34539663 | ||
| Essential role of YopD in inhibition of the respiratory burst of macrophages by Yersinia enterocolitica | Q34541189 | ||
| A genetic locus of enterocyte effacement conserved among diverse enterobacterial pathogens | Q34642972 | ||
| Fibronectin receptor structures in the VLA family of heterodimers | Q34684589 | ||
| Requirement for exported proteins in secretion through the invasion-associated type III system of Salmonella typhimurium. | Q34734272 | ||
| A cytolysin encoded by Salmonella is required for survival within macrophages | Q34979023 | ||
| Immunohistochemical and electron microscopic study of interaction of Yersinia enterocolitica serotype O8 with intestinal mucosa during experimental enteritis | Q35091831 | ||
| Differential clearance and host-pathogen interactions of YopE- and YopK- YopL- Yersinia pestis in BALB/c mice | Q35094337 | ||
| Cloning of regions required for contact hemolysis and entry into LLC-MK2 cells from Shigella sonnei form I plasmid: virF is a positive regulator gene for these phenotypes | Q35095347 | ||
| lcrH, a gene necessary for virulence of Yersinia pestis and for the normal response of Y. pestis to ATP and calcium | Q35095821 | ||
| Nucleotide sequence and transcription analysis of yop51 from Yersinia enterocolitica W22703. | Q41515875 | ||
| Comparison of the invasion strategies used by Salmonella cholerae-suis, Shigella flexneri and Yersinia enterocolitica to enter cultured animal cells: endosome acidification is not required for bacterial invasion or intracellular replication | Q41516620 | ||
| The plasmid-encoded Yop2b protein of Yersinia pseudotuberculosis is a virulence determinant regulated by calcium and temperature at the level of transcription | Q41517472 | ||
| The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1 -encoded trans-acting elements controlled by temperature and calcium | Q41517690 | ||
| Post-translational regulation of Lcr plasmid-mediated peptides in pesticinogenic Yersinia pestis | Q41518944 | ||
| Transcription of the yop regulon from Y. enterocolitica requires trans acting pYV and chromosomal genes | Q41519744 | ||
| Molecular cloning and expression of calcium-regulated, plasmid-coded proteins of Y. pseudotuberculosis | Q41520149 | ||
| Genetic analysis of the plasmid region controlling virulence in Yersinia enterocolitica 0:9 by Mini-Mu insertions and lac gene fusions | Q41522027 | ||
| Virulence plasmid-associated HeLa cell induced cytotoxicity of Yersinia pseudotuberculosis | Q41522328 | ||
| IpaB of Shigella flexneri causes entry into epithelial cells and escape from the phagocytic vacuole | Q41524587 | ||
| Genetic Analysis of Essential Plasmid Determinants of Pathogenicity in Yersinia pestis | Q41530578 | ||
| Nucleotide sequence of the invasion plasmid antigen B and C genes (ipaB and ipaC) of Shigella flexneri | Q42653350 | ||
| rho, a small GTP-binding protein, is essential for Shigella invasion of epithelial cells | Q42947720 | ||
| Molecular Basis of Gene-for-Gene Specificity in Bacterial Speck Disease of Tomato | Q43463829 | ||
| Erwinia chrysanthemi harpinEch: an elicitor of the hypersensitive response that contributes to soft-rot pathogenesis. | Q43818903 | ||
| Molecular comparison of virulence plasmids in Shigella and enteroinvasive Escherichia coli | Q43886182 | ||
| The contribution of exoproducts to virulence of Pseudomonas aeruginosa | Q43958510 | ||
| Elicitor- and wound-induced oxidative cross-linking of a proline-rich plant cell wall protein: A novel, rapid defense response | Q44668410 | ||
| The VirF protein from Shigella flexneri is a member of the AraC transcription factor superfamily and is highly homologous to Rns, a positive regulator of virulence genes in enterotoxigenic Escherichia coli | Q45048153 | ||
| Identification and characterization of TnphoA mutants of Salmonella that are unable to pass through a polarized MDCK epithelial cell monolayer | Q46076466 | ||
| Molecular characterization and hrp dependence of the avirulence gene avrPto from Pseudomonas syringae pv. tomato [corrected]. | Q46375280 | ||
| The bundle-forming pili of enteropathogenic Escherichia coli: transcriptional regulation by environmental signals | Q46411600 | ||
| Harpin, elicitor of the hypersensitive response produced by the plant pathogen Erwinia amylovora | Q47932082 | ||
| Enteropathogenic E. coli (EPEC) transfers its receptor for intimate adherence into mammalian cells | Q48042079 | ||
| A secreted effector protein of Salmonella dublin is translocated into eukaryotic cells and mediates inflammation and fluid secretion in infected ileal mucosa | Q48042710 | ||
| Transcriptional activation of Salmonella typhimurium invasion genes by a member of the phosphorylated response-regulator superfamily. | Q48058213 | ||
| SopE, a secreted protein of Salmonella dublin, is translocated into the target eukaryotic cell via a sip-dependent mechanism and promotes bacterial entry | Q48059335 | ||
| Attaching and effacing of host cells by enteropathogenic Escherichia coli in the absence of detectable tyrosine kinase mediated signal transduction. | Q48060524 | ||
| Interacting components of the flagellar motor of Escherichia coli revealed by the two-hybrid system in yeast | Q48066024 | ||
| The tomato gene Pti1 encodes a serine/threonine kinase that is phosphorylated by Pto and is involved in the hypersensitive response | Q48068497 | ||
| The hrpRS locus of Pseudomonas syringae pv. phaseolicola constitutes a complex regulatory unit | Q48076320 | ||
| The Salmonella typhimurium invasion genes invF and invG encode homologues of the AraC and PulD family of proteins | Q48080387 | ||
| Bacillus subtilis flagellar proteins FliP, FliQ, FliR and FlhB are related to Shigella flexneri virulence factors | Q48087031 | ||
| Pseudomonas syringae pv. syringae harpinPss: a protein that is secreted via the Hrp pathway and elicits the hypersensitive response in plants | Q48111472 | ||
| Protein secretion by gram-negative bacteria. Characterization of two membrane proteins required for pullulanase secretion by Escherichia coli K-12. | Q48284533 | ||
| A dual transcriptional activation system for the 230 kb plasmid genes coding for virulence-associated antigens of Shigella flexneri | Q48298555 | ||
| Partition of unit-copy miniplasmids to daughter cells. III. The DNA sequence and functional organization of the P1 partition region | Q48375246 | ||
| Unified nomenclature for broadly conserved hrp genes of phytopathogenic bacteria. | Q48786134 | ||
| The invasion-associated type III system of Salmonella typhimurium directs the translocation of Sip proteins into the host cell. | Q50134497 | ||
| Requirement of CDC42 for Salmonella-induced cytoskeletal and nuclear responses. | Q50136441 | ||
| Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium. | Q50136458 | ||
| Co-ordinate regulation of Salmonella typhimurium invasion genes by environmental and regulatory factors is mediated by control of hilA expression. | Q50136962 | ||
| Salmonella spp. are cytotoxic for cultured macrophages. | Q50137708 | ||
| Mg2+ as an extracellular signal: environmental regulation of Salmonella virulence. | Q50140541 | ||
| Salmonella typhimurium secreted invasion determinants are homologous to Shigella Ipa proteins. | Q50141720 | ||
| Functional conservation of the Salmonella and Shigella effectors of entry into epithelial cells. | Q50142773 | ||
| Preferential interaction of Salmonella typhimurium with mouse Peyer's patch M cells. | Q50147225 | ||
| Morphological pathway of flagellar assembly in Salmonella typhimurium. | Q50175027 | ||
| Initiation of Plant Disease Resistance by Physical Interaction of AvrPto and Pto Kinase | Q52522892 | ||
| Expression of avrPphB, an avirulence gene from Pseudomonas syringae pv. phaseolicola, and the delivery of signals causing the hypersensitive reaction in bean. | Q54570214 | ||
| A cloned pathogenicity island from enteropathogenic Escherichia coli confers the attaching and effacing phenotype on E. coli K-12. | Q54574143 | ||
| Expression of the Pseudomonas syringae avirulence protein AvrB in plant cells alleviates its dependence on the hypersensitive response and pathogenicity (Hrp) secretion system in eliciting genotype-specific hypersensitive cell death. | Q54586263 | ||
| Phenotypic expression of Pseudomonas syringae avr genes in E. coli is linked to the activities of the hrp-encoded secretion system. | Q54589765 | ||
| Analysis of the role of the Pseudomonas syringae pv. syringae HrpZ harpin in elicitation of the hypersensitive response in tobacco using functionally non-polar hrpZ deletion mutations, truncated HrpZ fragments, and hrmA mutations. | Q54594313 | ||
| pIV, a filamentous phage protein that mediates phage export across the bacterial cell envelope, forms a multimer. | Q54635177 | ||
| Expression of four virulence antigens of Shigella flexneri is positively regulated at the transcriptional level by the 30 kiloDalton virF protein. | Q54742538 | ||
| Tyrosine phosphorylation of the gamma subunit of Fc gamma receptors, p72syk, and paxillin during Fc receptor-mediated phagocytosis in macrophages. | Q54762133 | ||
| Recognition of the Bacterial Avirulence Protein AvrBs3 Occurs inside the Host Plant Cell | Q57266285 | ||
| Graphical interface for ProDom domain families | Q57935194 | ||
| Enhanced secretion through the Shigella flexneri Mxi-Spa translocon leads to assembly of extracellular proteins into macromolecular structures | Q64360979 | ||
| Nucleotide sequence of theipaBCDstructural genes ofShigella dysenteriae | Q67816422 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | type III protein secretion system complex | Q21199165 |
| type I protein secretion system complex | Q21760978 | ||
| P304 | page(s) | 379-433 | |
| P577 | publication date | 1998-06-01 | |
| P1433 | published in | Microbiology and Molecular Biology Reviews | Q6839270 |
| P1476 | title | Type III protein secretion systems in bacterial pathogens of animals and plants | |
| P478 | volume | 62 |
| Q54490058 | (1)H, (13)C, and (15)N resonance assignments of the EscJ protein, a structural component of the Type III secretion system of enteropathogenic E. coli (EPEC). |
| Q28822572 | 3'-NADP and 3'-NAADP - Two Metabolites Formed by the Bacterial Type III Effector AvrRxo1 |
| Q39793977 | A Burkholderia pseudomallei type III secreted protein, BopE, facilitates bacterial invasion of epithelial cells and exhibits guanine nucleotide exchange factor activity |
| Q42581042 | A C-terminal domain targets the Pseudomonas aeruginosa cytotoxin ExoU to the plasma membrane of host cells |
| Q35095963 | A C-terminal region of Yersinia pestis YscD binds the outer membrane secretin YscC |
| Q34364158 | A Genomic Island in Salmonella enterica ssp. salamae provides new insights on the genealogy of the locus of enterocyte effacement |
| Q33992012 | A HilA-independent pathway to Salmonella typhimurium invasion gene transcription |
| Q25257826 | A Role for the SmpB-SsrA system in Yersinia pseudotuberculosis pathogenesis |
| Q27349443 | A Salmonella small non-coding RNA facilitates bacterial invasion and intracellular replication by modulating the expression of virulence factors |
| Q64106351 | A Ubiquitous Platform for Bacterial Nanotube Biogenesis |
| Q37350400 | A bacterial sensor of plant cell contact controls the transcriptional induction of Ralstonia solanacearum pathogenicity genes. |
| Q28360416 | A bacterial type III secretion system inhibits actin polymerization to prevent pore formation in host cell membranes |
| Q34980175 | A chlamydial type III-secreted effector protein (Tarp) is predominantly recognized by antibodies from humans infected with Chlamydia trachomatis and induces protective immunity against upper genital tract pathologies in mice |
| Q24814370 | A computational approach for identifying pathogenicity islands in prokaryotic genomes |
| Q35162771 | A conserved amino acid sequence directing intracellular type III secretion by Salmonella typhimurium |
| Q34350887 | A cytotoxic type III secretion effector of Vibrio parahaemolyticus targets vacuolar H+-ATPase subunit c and ruptures host cell lysosomes |
| Q39892111 | A degenerate type III secretion system from septicemic Escherichia coli contributes to pathogenesis |
| Q41006822 | A dynamic and adaptive network of cytosolic interactions governs protein export by the T3SS injectisome |
| Q33315560 | A functional genomic yeast screen to identify pathogenic bacterial proteins |
| Q33279533 | A glimpse of streptococcal toxic shock syndrome from comparative genomics of S. suis 2 Chinese isolates |
| Q33850561 | A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae |
| Q90091525 | A highly conserved complete accessory Escherichia coli type III secretion system 2 is widespread in bloodstream isolates of the ST69 lineage |
| Q36646792 | A lysozyme-like protein in Brucella abortus is involved in the early stages of intracellular replication |
| Q58800559 | A metagenomic study of the gut microbiome in Behcet's disease |
| Q37212009 | A new pathway for the secretion of virulence factors by bacteria: the flagellar export apparatus functions as a protein-secretion system. |
| Q49830539 | A putative LysR-type transcriptional regulator PrhO positively regulates the type III secretion system and contributes to virulence of Ralstonia solanacearum. |
| Q36883886 | A safe bacterial microsyringe for in vivo antigen delivery and immunotherapy. |
| Q35421297 | A secreted Salmonella protein induces a proinflammatory response in epithelial cells, which promotes neutrophil migration |
| Q35029284 | A small-molecule inhibitor of type III secretion inhibits different stages of the infectious cycle of Chlamydia trachomatis |
| Q28538799 | A substrate-fusion protein is trapped inside the Type III Secretion System channel in Shigella flexneri |
| Q36576242 | A type III secretion system is required for Aeromonas hydrophila AH-1 pathogenesis |
| Q34008981 | Absence of all components of the flagellar export and synthesis machinery differentially alters virulence of Salmonella enterica serovar Typhimurium in models of typhoid fever, survival in macrophages, tissue culture invasiveness, and calf enterocol |
| Q36180764 | Abundant toxin-related genes in the genomes of beneficial symbionts from deep-sea hydrothermal vent mussels |
| Q33434470 | Accurate prediction of secreted substrates and identification of a conserved putative secretion signal for type III secretion systems |
| Q30403314 | Acquired type III secretion system determines environmental fitness of epidemic Vibrio parahaemolyticus in the interaction with bacterivorous protists |
| Q39655427 | Activation of the Pseudomonas aeruginosa type III secretion system requires an intact pyruvate dehydrogenase aceAB operon |
| Q34608900 | Adaptive evolution of relish, a Drosophila NF-kappaB/IkappaB protein |
| Q42570485 | Aeromonas hydrophila AH-3 type III secretion system expression and regulatory network. |
| Q24299950 | Alpha 1-antitrypsin binds to and interferes with functionality of EspB from atypical and typical enteropathogenic Escherichia coli strains |
| Q28492911 | An adenylate cyclase-controlled signaling network regulates Pseudomonas aeruginosa virulence in a mouse model of acute pneumonia |
| Q33937788 | An amino-terminal secretion signal is required for YplA export by the Ysa, Ysc, and flagellar type III secretion systems of Yersinia enterocolitica biovar 1B. |
| Q35177202 | An infrequent molecular ruler controls flagellar hook length in Salmonella enterica |
| Q40867738 | Analysis of an engineered Salmonella flagellar fusion protein, FliR-FlhB. |
| Q42957138 | Analysis of cell type-specific responses mediated by the type IV secretion system of Helicobacter pylori |
| Q33785722 | Analysis of interactions of Salmonella type three secretion mutants with 3-D intestinal epithelial cells |
| Q34048332 | Analysis of putative Chlamydia trachomatis chaperones Scc2 and Scc3 and their use in the identification of type III secretion substrates. |
| Q33996354 | Analysis of the PilQ secretin from Neisseria meningitidis by transmission electron microscopy reveals a dodecameric quaternary structure. |
| Q39391975 | Analysis of the contribution of Salmonella pathogenicity islands 1 and 2 to enteric disease progression using a novel bovine ileal loop model and a murine model of infectious enterocolitis |
| Q31160722 | Analysis of the prevalence, secretion and function of a cell cycle-inhibiting factor in the melioidosis pathogen Burkholderia pseudomallei |
| Q34941041 | Analysis of virulence and inflammatory potential of Shigella flexneri purine biosynthesis mutants |
| Q41380601 | Anti-PcrV antibody strategies against virulent Pseudomonas aeruginosa |
| Q37676924 | Anti-virulence strategies to combat bacteria-mediated disease |
| Q35194014 | Antibiotics as intermicrobial signaling agents instead of weapons |
| Q35741537 | Application of β-lactamase reporter fusions as an indicator of effector protein secretion during infections with the obligate intracellular pathogen Chlamydia trachomatis |
| Q33238585 | Assembly of the type III secretion apparatus of enteropathogenic Escherichia coli |
| Q52337397 | Assembly, Biochemical Characterization, Immunogenicity, Adjuvanticity, and Efficacy of Shigella Artificial Invaplex. |
| Q39230405 | Assembly, structure, function and regulation of type III secretion systems. |
| Q27013824 | Association between Pseudomonas aeruginosa type III secretion, antibiotic resistance, and clinical outcome: a review |
| Q35998321 | Attaching-effacing bacteria in animals |
| Q35011309 | Attenuated Yersinia pseudotuberculosis carrier vaccine for simultaneous antigen-specific CD4 and CD8 T-cell induction |
| Q34713775 | Attenuated virulence of a Burkholderia cepacia type III secretion mutant in a murine model of infection |
| Q39499980 | Autodisplay: functional display of active beta-lactamase on the surface of Escherichia coli by the AIDA-I autotransporter. |
| Q37205430 | Autophagic clearance of bacterial pathogens: molecular recognition of intracellular microorganisms |
| Q41362969 | Autoproteolysis of YscU of Yersinia pseudotuberculosis is important for regulation of expression and secretion of Yop proteins |
| Q37413404 | Azithromycin Attenuates Pseudomonas-Induced Lung Inflammation by Targeting Bacterial Proteins Secreted in the Cultured Medium. |
| Q33938208 | Azithromycin inhibits the formation of flagellar filaments without suppressing flagellin synthesis in Salmonella enterica serovar typhimurium |
| Q24548485 | Bacteria in the leaf ecosystem with emphasis on Pseudomonas syringae-a pathogen, ice nucleus, and epiphyte |
| Q46300728 | Bacterial Chat: Intestinal Metabolites and Signals in Host-Microbiota-Pathogen Interactions |
| Q40115511 | Bacterial effector NleL promotes enterohemorrhagic E. coli-induced attaching and effacing lesions by ubiquitylating and inactivating JNK. |
| Q24293521 | Bacterial effector binding to ribosomal protein s3 subverts NF-kappaB function |
| Q38634734 | Bacterial flagellin-a potent immunomodulatory agent. |
| Q35916694 | Bacterial menageries inside insects |
| Q34142106 | Bacterial nanomachines: the flagellum and type III injectisome. |
| Q35621482 | Bacterial pathogens and community composition in advanced sewage treatment systems revealed by metagenomics analysis based on high-throughput sequencing |
| Q37683337 | Bacterial serine/threonine protein kinases in host-pathogen interactions |
| Q58792122 | Bacterial type III secretion systems: a complex device for the delivery of bacterial effector proteins into eukaryotic host cells |
| Q27028058 | Bacterial type III secretion systems: specialized nanomachines for protein delivery into target cells |
| Q36370585 | Bacteriophage ST64B, a Genetic Mosaic of Genes from Diverse Sources Isolated fromSalmonella entericaSerovar Typhimurium DT 64 |
| Q24537501 | Bacteriophage control of bacterial virulence |
| Q33712790 | Bacteriophages in the evolution of pathogen-host interactions |
| Q37040231 | Bartonella and Brucella--weapons and strategies for stealth attack |
| Q37077823 | Beyond good and evil in the oral cavity: insights into host-microbe relationships derived from transcriptional profiling of gingival cells |
| Q28533925 | Biochemical characterization of UDP-N-acetylmuramoyl-L-alanyl-D-glutamate: meso-2,6-diaminopimelate ligase (MurE) from Verrucomicrobium spinosum DSM 4136(T.) |
| Q34328046 | Biochemical characterization of the Yersinia YopT protease: cleavage site and recognition elements in Rho GTPases |
| Q31110190 | Biodiversity of vibrios |
| Q28484742 | Bioinformatic and biochemical evidence for the identification of the type III secretion system needle protein of Chlamydia trachomatis |
| Q24791468 | Bioinformatics analysis of the locus for enterocyte effacement provides novel insights into type-III secretion |
| Q34851073 | Biophysical characterization of Chlamydia trachomatis CT584 supports its potential role as a type III secretion needle tip protein |
| Q37834004 | Biphasic Metabolism and Host Interaction of a Chlamydial Symbiont |
| Q36483610 | Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
| Q38202459 | Building a secreting nanomachine: a structural overview of the T3SS. |
| Q38926185 | CRISPR-Cas and Contact-Dependent Secretion Systems Present on Excisable Pathogenicity Islands with Conserved Recombination Modules |
| Q42145953 | Calcium and iron regulate swarming and type III secretion in Vibrio parahaemolyticus |
| Q34344839 | Candidatus Sodalis melophagi sp. nov.: phylogenetically independent comparative model to the tsetse fly symbiont Sodalis glossinidius |
| Q34678595 | Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria. |
| Q42566826 | Caspase-1-mediated activation of interleukin-1beta (IL-1beta) and IL-18 contributes to innate immune defenses against Salmonella enterica serovar Typhimurium infection |
| Q39512990 | Cell death of human polymorphonuclear neutrophils induced by a Pseudomonas aeruginosa cystic fibrosis isolate requires a functional type III secretion system |
| Q33991711 | Cellular locations of Pseudomonas syringae pv. syringae HrcC and HrcJ proteins, required for harpin secretion via the type III pathway. |
| Q39741755 | CesD2 of enteropathogenic Escherichia coli is a second chaperone for the type III secretion translocator protein EspD. |
| Q34713695 | Change is good: variations in common biological mechanisms in the epsilonproteobacterial genera Campylobacter and Helicobacter |
| Q33884633 | Changes in race-specific virulence in Pseudomonas syringae pv. phaseolicola are associated with a chimeric transposable element and rare deletion events in a plasmid-borne pathogenicity island |
| Q39527110 | Characterization and mutational analysis of three allelic lsc genes encoding levansucrase in Pseudomonas syringae |
| Q33994963 | Characterization of SepL of enterohemorrhagic Escherichia coli |
| Q40477349 | Characterization of an ExoS Type III translocation-resistant cell line. |
| Q43422418 | Characterization of molten globule PopB in absence and presence of its chaperone PcrH. |
| Q61810394 | Characterization of the Mode of Action of Aurodox, a Type III Secretion System Inhibitor from Streptomyces goldiniensis |
| Q37133792 | Characterization of the NleF effector protein from attaching and effacing bacterial pathogens. |
| Q40389859 | Characterization of the Ruler Protein Interaction Interface on the Substrate Specificity Switch Protein in the Yersinia Type III Secretion System |
| Q37032486 | Characterization of the Shigella and Salmonella Type III Secretion System Tip-Translocon Protein-Protein Interaction by Paramagnetic Relaxation Enhancement |
| Q40867634 | Characterization of the cis-acting regulatory element controlling HrpB-mediated activation of the type III secretion system and effector genes in Ralstonia solanacearum. |
| Q37182191 | Characterization of the expression of Salmonella Type III secretion system factor PrgI, SipA, SipB, SopE2, SpaO, and SptP in cultures and in mice |
| Q79204518 | Characterization of the hrp pathogenicity cluster of Erwinia carotovora subsp. carotovora: high basal level expression in a mutant is associated with reduced virulence |
| Q33736489 | Characterization of the hrpC and hrpRS operons of Pseudomonas syringae pathovars syringae, tomato, and glycinea and analysis of the ability of hrpF, hrpG, hrcC, hrpT, and hrpV mutants to elicit the hypersensitive response and disease in plants |
| Q37856790 | Characterization of the putative type III secretion ATPase CdsN (Cpn0707) of Chlamydophila pneumoniae |
| Q42116577 | Characterization of the self-cleaving effector protein NopE1 of Bradyrhizobium japonicum |
| Q28475654 | Chemical genetics reveals bacterial and host cell functions critical for type IV effector translocation by Legionella pneumophila |
| Q36255142 | Chlamydia psittaci comparative genomics reveals intraspecies variations in the putative outer membrane and type III secretion system genes. |
| Q36950073 | Chlamydial effector proteins localized to the host cell cytoplasmic compartment |
| Q35634235 | Chlamydial type III secretion system is encoded on ten operons preceded by sigma 70-like promoter elements |
| Q30168366 | Chunnel vision. Export and efflux through bacterial channel-tunnels |
| Q35019815 | Cis-2-dodecenoic acid signal modulates virulence of Pseudomonas aeruginosa through interference with quorum sensing systems and T3SS |
| Q64071132 | Classical Soybean () Symbionts, USDA191 and USDA110, Reveal Contrasting Symbiotic Phenotype on Pigeon Pea ( (L.) Millsp) |
| Q34855945 | Cloning and characterization of an Ehrlichia canis gene encoding a protein localized to the morula membrane |
| Q36208325 | Co-regulation of Iron Metabolism and Virulence Associated Functions by Iron and XibR, a Novel Iron Binding Transcription Factor, in the Plant Pathogen Xanthomonas |
| Q27664968 | Combination of Two Separate Binding Domains Defines Stoichiometry between Type III Secretion System Chaperone IpgC and Translocator Protein IpaB |
| Q42450071 | Common and distinct structural features of Salmonella injectisome and flagellar basal body |
| Q27023604 | Commonalities and differences of T3SSs in rhizobia and plant pathogenic bacteria |
| Q30010247 | Comparative analysis of EspF variants in inhibition of Escherichia coli phagocytosis by macrophages and inhibition of E. coli translocation through human- and bovine-derived M cells. |
| Q40403768 | Comparative analysis of Salmonella enterica serovar Typhimurium biofilm formation on gallstones and on glass |
| Q33714608 | Comparative genomic analysis of the pPT23A plasmid family of Pseudomonas syringae |
| Q64914632 | Comparative genomics and genome biology of Campylobacter showae. |
| Q37508139 | Comparative genomics of aeschynomene symbionts: insights into the ecological lifestyle of nod-independent photosynthetic bradyrhizobia. |
| Q46882359 | Comparative large-scale analysis of interactions between several crop species and the effector repertoires from multiple pathovars of Pseudomonas and Ralstonia |
| Q42221777 | Comparative proteomic analysis reveals that T3SS, Tfp, and xanthan gum are key factors in initial stages of Citrus sinensis infection by Xanthomonas citri subsp. citri |
| Q34312033 | Comparative sequence analysis of the symbiosis island of Mesorhizobium loti strain R7A. |
| Q37552900 | Comparison of ATPase-encoding type III secretion system hrcN genes in biocontrol fluorescent Pseudomonads and in phytopathogenic proteobacteria |
| Q36376664 | Comparison of two major forms of the Shigella virulence plasmid pINV: positive selection is a major force driving the divergence |
| Q35067020 | Complete genome sequence of a Yersinia enterocolitica "Old World" (3/O:9) strain and comparison with the "New World" (1B/O:8) strain |
| Q21092477 | Complete genome sequence of the N2-fixing broad host range endophyte Klebsiella pneumoniae 342 and virulence predictions verified in mice |
| Q33521772 | Complete genome sequence of the fire blight pathogen Erwinia pyrifoliae DSM 12163T and comparative genomic insights into plant pathogenicity |
| Q24682539 | Complete genome sequence of the oral pathogenic Bacterium porphyromonas gingivalis strain W83 |
| Q33789355 | Complex function for SicA, a Salmonella enterica serovar typhimurium type III secretion-associated chaperone |
| Q40388345 | Components and dynamics of fiber formation define a ubiquitous biogenesis pathway for bacterial pili |
| Q39494402 | Components of the Salmonella flagellar export apparatus and classification of export substrates |
| Q27313367 | Composition, formation, and regulation of the cytosolic c-ring, a dynamic component of the type III secretion injectisome |
| Q36637597 | Computational modeling and experimental validation of the Legionella and Coxiella virulence-related type-IVB secretion signal |
| Q37319107 | Computational prediction shines light on type III secretion origins |
| Q34167887 | Concerted actions of a thermo-labile regulator and a unique intergenic RNA thermosensor control Yersinia virulence |
| Q34261693 | Concomitant cytosolic delivery of two immunodominant listerial antigens by Salmonella enterica serovar typhimurium confers superior protection against murine listeriosis |
| Q50102246 | Construction and evaluation of type III secretion system mutants of the catfish pathogen Edwardsiella piscicida. |
| Q33736851 | Construction of a Tn5-tagged mutant library of Xanthomonas oryzae pv. oryzicola as an invaluable resource for functional genomics |
| Q57023074 | Contribution of SPI-1 bistability to Salmonella enterica cooperative virulence: insights from single cell analysis |
| Q33917651 | Contribution of Salmonella typhimurium type III secretion components to needle complex formation |
| Q33768993 | Contribution of Vibrio parahaemolyticus virulence factors to cytotoxicity, enterotoxicity, and lethality in mice |
| Q33701821 | Control of type III protein secretion using a minimal genetic system |
| Q40017377 | Coordinated regulation of expression of Salmonella pathogenicity island 1 and flagellar type III secretion systems by ATP-dependent ClpXP protease |
| Q35867616 | Correlating levels of type III secretion and secreted proteins with fecal shedding of Escherichia coli O157:H7 in cattle |
| Q30443448 | Cortactin and Crk cooperate to trigger actin polymerization during Shigella invasion of epithelial cells |
| Q34010272 | Coupling of flagellar gene expression to flagellar assembly in Salmonella enterica serovar typhimurium and Escherichia coli |
| Q38280669 | Cross-species cluster co-conservation: a new method for generating protein interaction networks |
| Q52836587 | Cross-talk between a regulatory small RNA, cyclic-di-GMP signalling and flagellar regulator FlhDC for virulence and bacterial behaviours. |
| Q27665064 | Crystal Structure of Legionella DotD: Insights into the Relationship between Type IVB and Type II/III Secretion Systems |
| Q30475802 | Crystal structure of the flagellar rotor protein FliN from Thermotoga maritima |
| Q34553002 | Crystallization and preliminary X-ray diffraction analysis of BipD, a virulence factor from Burkholderia pseudomallei |
| Q28472041 | Cytosolic extract induces Tir translocation and pedestals in EPEC-infected red blood cells |
| Q40004916 | Cytosporone B, an inhibitor of the type III secretion system of Salmonella enterica serovar Typhimurium |
| Q35185082 | Cytotoxicity of Pseudomonas secreted exotoxins requires OxyR expression |
| Q33955395 | DBSecSys: a database of Burkholderia mallei secretion systems. |
| Q35657182 | DNA adenine methylase mutants of Salmonella typhimurium show defects in protein secretion, cell invasion, and M cell cytotoxicity |
| Q30385745 | DNA-Binding Protein HU Coordinates Pathogenicity in Vibrio parahaemolyticus |
| Q33490644 | Deciphering Evolutionary Mechanisms Between Mutualistic and Pathogenic Symbioses |
| Q35213234 | Deciphering chicken gut microbial dynamics based on high-throughput 16S rRNA metagenomics analyses |
| Q54286218 | Derivative of plant phenolic compound inhibits the type III secretion system of Dickeya dadantii via HrpX/HrpY two-component signal transduction and Rsm systems. |
| Q34039055 | Derivatives of plant phenolic compound affect the type III secretion system of Pseudomonas aeruginosa via a GacS-GacA two-component signal transduction system |
| Q33530126 | Designed coiled-coil peptides inhibit the type three secretion system of enteropathogenic Escherichia coli |
| Q24793934 | Detection and characterization of the S. typhimurium HilA protein |
| Q33755197 | Detection of and response to signals involved in host-microbe interactions by plant-associated bacteria |
| Q40782943 | Determination of the Stoichiometry of the Complete Bacterial Type III Secretion Needle Complex Using a Combined Quantitative Proteomic Approach |
| Q34290792 | Development of two animal models to study the function of Vibrio parahaemolyticus type III secretion systems. |
| Q27646583 | Differences in the Electrostatic Surfaces of the Type III Secretion Needle Proteins PrgI, BsaL, and MxiH |
| Q33928888 | Differential expression of Salmonella type III secretion system factors InvJ, PrgJ, SipC, SipD, SopA and SopB in cultures and in mice |
| Q39741576 | Differential modulation by Ca2+ of type III secretion of diffusely adhering enteropathogenic Escherichia coli |
| Q37118484 | Differential protein expression by Porphyromonas gingivalis in response to secreted epithelial cell components |
| Q34001486 | Differential regulation of Salmonella typhimurium type III secreted proteins by pathogenicity island 1 (SPI-1)-encoded transcriptional activators InvF and hilA. |
| Q41923043 | Dimerization of the Agrobacterium tumefaciens VirB4 ATPase and the effect of ATP-binding cassette mutations on the assembly and function of the T-DNA transporter |
| Q33533545 | Discovery and characterization of inhibitors of Pseudomonas aeruginosa type III secretion |
| Q36804209 | Distinct isoforms of phospholipase A2 mediate the ability of Salmonella enterica serotype typhimurium and Shigella flexneri to induce the transepithelial migration of neutrophils |
| Q41826228 | Distribution of flagella secreted protein and integral membrane protein among Campylobacter jejuni isolated from Thailand |
| Q34143709 | Distribution of tccP in clinical enterohemorrhagic and enteropathogenic Escherichia coli isolates |
| Q33348348 | Distribution of the secondary type III secretion system locus found in enterohemorrhagic Escherichia coli O157:H7 isolates among Shiga toxin-producing E. coli strains |
| Q35598624 | Disulfide bonding within components of the Chlamydia type III secretion apparatus correlates with development |
| Q37095412 | Docking of cytosolic chaperone-substrate complexes at the membrane ATPase during flagellar type III protein export |
| Q36201930 | Domain analyses reveal that Chlamydia trachomatis CT694 protein belongs to the membrane-localized family of type III effector proteins |
| Q40735820 | Downregulation of mitogen-activated protein kinases by the Bordetella bronchiseptica Type III secretion system leads to attenuated nonclassical macrophage activation |
| Q39496993 | DsbA is required for stable expression of outer membrane protein YscC and for efficient Yop secretion in Yersinia pestis |
| Q37298457 | Dysbiosis of small intestinal microbiota in liver cirrhosis and its association with etiology |
| Q38337459 | EHEC Adhesins |
| Q34041909 | Early immune response to the components of the type III system of Pseudomonas aeruginosa in children with cystic fibrosis |
| Q36575720 | Effect of metabolic imbalance on expression of type III secretion genes in Pseudomonas aeruginosa |
| Q34672479 | Effective identification of bacterial type III secretion signals using joint element features. |
| Q36046827 | Effector ExoU from the type III secretion system is an important modulator of gene expression in lung epithelial cells in response to Pseudomonas aeruginosa infection |
| Q24797978 | Effects of monoclonal anti-PcrV antibody on Pseudomonas aeruginosa-induced acute lung injury in a rat model |
| Q33965276 | Efficient isolation of Pseudomonas aeruginosa type III secretion translocators and assembly of heteromeric transmembrane pores in model membranes |
| Q35091765 | Electroporation of functional bacterial effectors into mammalian cells |
| Q28290909 | Endofungal bacterium controls its host by an hrp type III secretion system |
| Q37105856 | Enhanced Type III Secretion System Expression of Atypical Shigella flexneri II:(3)4,7(8). |
| Q33996908 | Enhancer-binding proteins HrpR and HrpS interact to regulate hrp-encoded type III protein secretion in Pseudomonas syringae strains |
| Q56949011 | Enhancing functional expression of heterologous lipase B in Escherichia coli by extracellular secretion |
| Q49352515 | Enterococcus faecalis Hydrolyzes Dental Resin Composites and Adhesives. |
| Q33604552 | Enteropathogenic E. coli, Salmonella, and Shigella: masters of host cell cytoskeletal exploitation |
| Q39518696 | Enteropathogenic Escherichia coli (EPEC) Tir receptor molecule does not undergo full modification when introduced into host cells by EPEC-independent mechanisms |
| Q34584852 | Enteropathogenic Escherichia coli mediates antiphagocytosis through the inhibition of PI 3-kinase-dependent pathways |
| Q36104202 | Enteropathogenic and enterohemorrhagic Escherichia coli infections: translocation, translocation, translocation |
| Q39539230 | Enzymology of type IV macromolecule secretion systems: the conjugative transfer regions of plasmids RP4 and R388 and the cag pathogenicity island of Helicobacter pylori encode structurally and functionally related nucleoside triphosphate hydrolases |
| Q30374743 | Epidemiology of Vibrio parahaemolyticus outbreaks, southern Chile. |
| Q33245158 | Epigenetic acquisition of inducibility of type III cytotoxicity in P. aeruginosa |
| Q37873105 | Epithelial cells infected with Chlamydophila pneumoniae (Chlamydia pneumoniae) are resistant to apoptosis. |
| Q35006658 | Eradication of intracellular Salmonella enterica serovar Typhimurium with a small-molecule, host cell-directed agent |
| Q36911591 | EscE and EscG are cochaperones for the type III needle protein EscF of enteropathogenic Escherichia coli |
| Q40600401 | EscO, a functional and structural analog of the flagellar FliJ protein, is a positive regulator of EscN ATPase activity of the enteropathogenic Escherichia coli injectisome |
| Q27022139 | Escherichia coli type III secretion system 2: a new kind of T3SS? |
| Q40642146 | EseE of Edwardsiella tarda Augments Secretion of Translocon Protein EseC and Expression of the escC-eseE Operon |
| Q30276039 | Evolution of atypical enteropathogenic E. coli by repeated acquisition of LEE pathogenicity island variants |
| Q40382973 | Examination of the coordinate effects of Pseudomonas aeruginosa ExoS on Rac1. |
| Q47142170 | Excess labile carbon promotes the expression of virulence factors in coral reef bacterioplankton |
| Q41769175 | Exoenzyme S shows selective ADP-ribosylation and GTPase-activating protein (GAP) activities towards small GTPases in vivo |
| Q34351123 | Expression analysis of a highly adherent and cytotoxic small colony variant of Pseudomonas aeruginosa isolated from a lung of a patient with cystic fibrosis |
| Q37713167 | Expression and targeting of secreted proteins from Chlamydia trachomatis. |
| Q39517996 | Expression of ExsA in trans confers type III secretion system-dependent cytotoxicity on noncytotoxic Pseudomonas aeruginosa cystic fibrosis isolates |
| Q35220416 | Expression of Pseudomonas aeruginosa toxin ExoS effectively induces apoptosis in host cells |
| Q35892833 | Expression of a functional secreted YopN-TyeA hybrid protein in Yersinia pestis is the result of a +1 translational frameshift event |
| Q34079370 | Expression of microbial virulence proteins in Saccharomyces cerevisiae models mammalian infection |
| Q44553890 | Expression profiles of pea pathogenicity ( PEP) genes in vivo and in vitro, characterization of the flanking regions of the PEP cluster and evidence that the PEP cluster region resulted from horizontal gene transfer in the fungal pathogen Nectria ha |
| Q40945901 | Expression profiling of virulence and pathogenicity genes of Xanthomonas axonopodis pv. citri. |
| Q37475018 | ExsE Is a Negative Regulator for T3SS Gene Expression in Vibrio alginolyticus. |
| Q33497618 | Extracellular secretion of Carocin S1 in Pectobacterium carotovorum subsp. carotovorum occurs via the type III secretion system integral to the bacterial flagellum |
| Q33949995 | Flagellin stimulation of intestinal epithelial cells triggers CCL20-mediated migration of dendritic cells. |
| Q27662152 | FlhA provides the adaptor for coordinated delivery of late flagella building blocks to the type III secretion system |
| Q39521493 | FlhA, a component of the flagellum assembly apparatus of Pseudomonas aeruginosa, plays a role in internalization by corneal epithelial cells |
| Q44058928 | Fluorescence-Reported Allelic Exchange Mutagenesis Reveals a Role for Chlamydia trachomatis TmeA in Invasion That Is Independent of Host AHNAK. |
| Q42023974 | Formation of a novel surface structure encoded by Salmonella Pathogenicity Island 2. |
| Q27026390 | From screen to target: insights and approaches for the development of anti-virulence compounds |
| Q34181996 | Fructose-bisphophate aldolase exhibits functional roles between carbon metabolism and the hrp system in rice pathogen Xanthomonas oryzae pv. oryzicola |
| Q39235366 | Functional Characterization of EscK (Orf4), a Sorting Platform Component of the Enteropathogenic Escherichia coli Injectisome |
| Q30320829 | Functional analysis of HrpF, a putative type III translocon protein from Xanthomonas campestris pv. vesicatoria |
| Q37410187 | Functional characterization of SsaE, a novel chaperone protein of the type III secretion system encoded by Salmonella pathogenicity island 2. |
| Q28490001 | Functional characterization of the type III secretion ATPase SsaN encoded by Salmonella pathogenicity island 2 |
| Q37582870 | Functional characterization of two type III secretion systems of Vibrio parahaemolyticus |
| Q29346800 | Functional domains of ExsA, the transcriptional activator of the Pseudomonas aeruginosa type III secretion system |
| Q37196207 | Functional genomic analyses of Enterobacter, Anopheles and Plasmodium reciprocal interactions that impact vector competence. |
| Q33558698 | Functional regions of the Pseudomonas aeruginosa cytotoxin ExoU |
| Q26995596 | Förster resonance energy transfer (FRET) as a tool for dissecting the molecular mechanisms for maturation of the Shigella type III secretion needle tip complex |
| Q24319756 | GEF-H1 mediated control of NOD1 dependent NF-kappaB activation by Shigella effectors |
| Q33988425 | Gene integration and expression and extracellular secretion of Erwinia chrysanthemi endoglucanase CelY (celY) and CelZ (celZ) in ethanologenic Klebsiella oxytoca P2. |
| Q39678808 | Gene transfer between Salmonella enterica serovar Typhimurium inside epithelial cells |
| Q34301243 | Generation and Characterization of a scFv Antibody Against T3SS Needle of Vibrio parahaemolyticus |
| Q33995538 | Genetic analysis of assembly of the Salmonella enterica serovar Typhimurium type III secretion-associated needle complex. |
| Q33979924 | Genetic characterization of conserved charged residues in the bacterial flagellar type III export protein FlhA |
| Q64123672 | Genome analysis of Pseudomonas syringae pv. actinidiae biovar 6, which produces the phytotoxins, phaseolotoxin and coronatine |
| Q30984768 | Genome comparison of the epiphytic bacteria Erwinia billingiae and E. tasmaniensis with the pear pathogen E. pyrifoliae. |
| Q24608507 | Genome degeneration and adaptation in a nascent stage of symbiosis |
| Q24655631 | Genome sequence of the beta-rhizobium Cupriavidus taiwanensis and comparative genomics of rhizobia |
| Q22065998 | Genome sequences of Chlamydia trachomatis MoPn and Chlamydia pneumoniae AR39. |
| Q34036110 | Genome sequencing and our understanding of chlamydiae |
| Q34505744 | Genome-wide analysis of the Pho regulon in a pstCA mutant of Citrobacter rodentium |
| Q30401150 | Genomes of the most dangerous epidemic bacteria have a virulence repertoire characterized by fewer genes but more toxin-antitoxin modules |
| Q35666138 | Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens |
| Q31032708 | Genomic approach for analysis of surface proteins in Chlamydia pneumoniae |
| Q35634482 | Genomic basis of endosymbiont-conferred protection against an insect parasitoid |
| Q30350256 | Genomic characterization of non-O1, non-O139 Vibrio cholerae reveals genes for a type III secretion system. |
| Q47236641 | Genomic features of bacterial adaptation to plants. |
| Q30320765 | Getting across--bacterial type III effector proteins on their way to the plant cell |
| Q34001946 | Global dissemination of Vibrio parahaemolyticus serotype O3:K6 and its serovariants |
| Q33374642 | Global transcriptional response to mammalian temperature provides new insight into Francisella tularensis pathogenesis |
| Q24644676 | Glucoamylase-like domains in the alpha- and beta-subunits of phosphorylase kinase |
| Q35086324 | Growth of Coxiella burnetii in the Ixodes scapularis-derived IDE8 tick cell line |
| Q34981697 | Hamiltonella defensa, genome evolution of protective bacterial endosymbiont from pathogenic ancestors |
| Q36044928 | Heterogeneous Surface Expression of EspA Translocon Filaments by Escherichia coli O157:H7 Is Controlled at the Posttranscriptional Level |
| Q33997017 | Hha is a negative modulator of transcription of hilA, the Salmonella enterica serovar Typhimurium invasion gene transcriptional activator |
| Q31082765 | High extracellular levels of Mycobacterium tuberculosis glutamine synthetase and superoxide dismutase in actively growing cultures are due to high expression and extracellular stability rather than to a protein-specific export mechanism |
| Q34374477 | Hijacking of leguminous nodulation signaling by the rhizobial type III secretion system |
| Q34714166 | HilE interacts with HilD and negatively regulates hilA transcription and expression of the Salmonella enterica serovar Typhimurium invasive phenotype. |
| Q40596580 | HopX1 in Erwinia amylovora functions as an avirulence protein in apple and is regulated by HrpL. |
| Q37374881 | Horizontal gene transfer: sustaining pathogenicity and optimizing host-pathogen interactions |
| Q42782111 | Hpa2 required by HrpF to translocate Xanthomonas oryzae transcriptional activator-like effectors into rice for pathogenicity |
| Q43843424 | HpaP modulates type III effector secretion in Ralstonia solanacearum and harbours a substrate specificity switch domain essential for virulence. |
| Q33598843 | Human response to Escherichia coli O157:H7 infection: antibodies to secreted virulence factors |
| Q37839872 | Hypothetical protein CT398 (CdsZ) interacts with σ(54) (RpoN)-holoenzyme and the type III secretion export apparatus in Chlamydia trachomatis |
| Q33955487 | Identification and analysis of bacterial virulence genes in vivo |
| Q92515642 | Identification and characterization of putative Aeromonas spp. T3SS effectors |
| Q33913383 | Identification and characterization of putative virulence genes and gene clusters in Aeromonas hydrophila PPD134/91 |
| Q37703068 | Identification and discrimination of Burkholderia pseudomallei, B. mallei, and B. thailandensis by real-time PCR targeting type III secretion system genes |
| Q28534112 | Identification and molecular characterization of YsaL (Ye3555): a novel negative regulator of YsaN ATPase in type three secretion system of enteropathogenic bacteria Yersinia enterocolitica |
| Q37442460 | Identification of Chlamydia trachomatis CT621, a protein delivered through the type III secretion system to the host cell cytoplasm and nucleus. |
| Q36187760 | Identification of Mycobacterium avium subsp. hominissuis secreted proteins using an in vitro system mimicking the phagosomal environment |
| Q35949246 | Identification of Pseudomonas syringae pv. syringae 61 type III secretion system Hrp proteins that can travel the type III pathway and contribute to the translocation of effector proteins into plant cells |
| Q39587251 | Identification of SopE2, a Salmonella secreted protein which is highly homologous to SopE and involved in bacterial invasion of epithelial cells |
| Q28293400 | Identification of SycN, YscX, and YscY, three new elements of the Yersinia yop virulon |
| Q42688335 | Identification of Vibrio cholerae type III secretion system effector proteins |
| Q37851947 | Identification of a family of effectors secreted by the type III secretion system that are conserved in pathogenic Chlamydiae |
| Q40705484 | Identification of a novel Citrobacter rodentium type III secreted protein, EspI, and roles of this and other secreted proteins in infection |
| Q38676435 | Identification of bacterial target proteins for the salicylidene acylhydrazide class of virulence-blocking compounds. |
| Q35111099 | Identification of mammalian proteins that collaborate with type III secretion system function: involvement of a chemokine receptor in supporting translocon activity |
| Q42651061 | Identification of new protein-protein interactions involving the products of the chromosome- and plasmid-encoded type IV secretion loci of the phytopathogen Xanthomonas axonopodis pv. citri |
| Q34033494 | Identification of new secreted effectors in Salmonella enterica serovar Typhimurium |
| Q59575223 | Identification of plant-regulated genes in Ustilago maydis by enhancer-trapping mutagenesis |
| Q43197028 | Identification of proteins secreted via Vibrio parahaemolyticus type III secretion system 1. |
| Q39680871 | Identification of the cis-acting site involved in activation of promoters regulated by activity of the type III secretion apparatus in Shigella flexneri |
| Q37008377 | Identification of the secretion and translocation domain of the enteropathogenic and enterohemorrhagic Escherichia coli effector Cif, using TEM-1 beta-lactamase as a new fluorescence-based reporter |
| Q33601534 | Identification of two novel hrp-associated genes in the hrp gene cluster of Xanthomonas oryzae pv. oryzae |
| Q36845195 | Identification of two translocon proteins of Vibrio parahaemolyticus type III secretion system 2 |
| Q52318660 | Identification of virulence factors and type III effectors of phylotype I, Indian Ralstonia solanacearum strains Rs-09-161 and Rs-10-244. |
| Q41388956 | In Silico Molecular Characterization of Cysteine Protease YopT from Yersinia pestis by Homology Modeling and Binding Site Identification |
| Q37701432 | In silico functional elucidation of uncharacterized proteins of Chlamydia abortus strain LLG. |
| Q34009568 | In vivo genetic analysis indicates that PhoP-PhoQ and the Salmonella pathogenicity island 2 type III secretion system contribute independently to Salmonella enterica serovar Typhimurium virulence |
| Q30155524 | In vivo versus in vitro protein abundance analysis of Shigella dysenteriae type 1 reveals changes in the expression of proteins involved in virulence, stress and energy metabolism |
| Q33517849 | Inactivation of the fliY gene encoding a flagellar motor switch protein attenuates mobility and virulence of Leptospira interrogans strain Lai. |
| Q33553163 | Induction of interferon-stimulated genes by Chlamydia pneumoniae in fibroblasts is mediated by intracellular nucleotide-sensing receptors. |
| Q36992556 | Induction of type III secretion by cell-free Chlamydia trachomatis elementary bodies |
| Q64110671 | Infection in Chronic Inflammation and Gastrointestinal Cancer |
| Q33816592 | Inflammasomes are important mediators of cyclophosphamide-induced bladder inflammation |
| Q33999966 | Influence of the Salmonella typhimurium pathogenicity island 2 type III secretion system on bacterial growth in the mouse. |
| Q39488192 | Ingested blood contributes to the specificity of the symbiosis of Aeromonas veronii biovar sobria and Hirudo medicinalis, the medicinal leech |
| Q46727572 | Inheritance of Pantoea type III secretion systems through both vertical and horizontal transfer |
| Q41209709 | Inhibition of expression of virulence genes of Yersinia pestis in Escherichia coli by external guide sequences and RNase P. |
| Q40065562 | Inhibitory effect of obovatol from Magnolia obovata on the Salmonella type III secretion system |
| Q60949777 | InnB, a Novel Type III Effector of USDA61, Controls Symbiosis With Species |
| Q35855643 | Innate and procured immunity inside the digestive tract of the medicinal leech |
| Q34357994 | Innate immune detection of bacterial virulence factors via the NLRC4 inflammasome |
| Q34161941 | Innate recognition of bacteria by a macrophage cytosolic surveillance pathway |
| Q30661663 | Integrating metagenomic and amplicon databases to resolve the phylogenetic and ecological diversity of the Chlamydiae |
| Q30734993 | Inter- and intraclonal diversity of the Pseudomonas aeruginosa proteome manifests within the secretome |
| Q37865819 | Interaction between components of the type III secretion system of Chlamydiaceae |
| Q35839659 | Interaction between innate immune cells and a bacterial type III secretion system in mutualistic and pathogenic associations. |
| Q36083389 | Interactions of Salmonella with host cells: encounters of the closest kind |
| Q37111200 | Interactions of the intestinal epithelium with the pathogen and the indigenous microbiota: a three-way crosstalk |
| Q39514613 | Interferon consensus sequence binding protein confers resistance against Yersinia enterocolitica |
| Q39502769 | Intergenic suppression between the flagellar MS ring protein FliF of Salmonella and FlhA, a membrane component of its export apparatus |
| Q35159314 | Interleukin-10 and inhibition of innate immunity to Yersiniae: roles of Yops and LcrV (V antigen) |
| Q35028632 | Internalization of Escherichia coli o157:h7 by bovine rectal epithelial cells |
| Q33792217 | InvB is a type III secretion chaperone specific for SspA. |
| Q33598570 | Invasion genes are not required for Salmonella enterica serovar typhimurium to breach the intestinal epithelium: evidence that salmonella pathogenicity island 1 has alternative functions during infection |
| Q41808436 | Investigations of Salmonella enterica serovar newport infections of oysters by using immunohistochemistry and knockout mutagenesis |
| Q42654425 | Involvement of NpdA, a Putative 2-Nitropropane Dioxygenase, in the T3SS Expression and Full Virulence in Ralstonia solanacearum OE1-1. |
| Q33196595 | Involvement of the intermediate filament protein cytokeratin-18 in actin pedestal formation during EPEC infection |
| Q42206130 | IpaC induces actin polymerization and filopodia formation during Shigella entry into epithelial cells |
| Q40454544 | IpaD of Shigella flexneri is independently required for regulation of Ipa protein secretion and efficient insertion of IpaB and IpaC into host membranes. |
| Q33749032 | IscR is essential for yersinia pseudotuberculosis type III secretion and virulence |
| Q30669730 | Isolation of Helicobacter pylori genes that modulate urease activity |
| Q36437267 | Isolation of a temperate bacteriophage encoding the type III effector protein SopE from an epidemic Salmonella typhimurium strain |
| Q99604969 | Keeping in Touch with Type-III Secretion System Effectors: Mass Spectrometry-Based Proteomics to Study Effector-Host Protein-Protein Interactions |
| Q39516954 | Key role for DsbA in cell-to-cell spread of Shigella flexneri, permitting secretion of Ipa proteins into interepithelial protrusions |
| Q28776658 | Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis |
| Q39416495 | Knots Untie: Molecular Determinants Involved in Knot Formation Induced by Pseudomonas savastanoi in Woody Hosts. |
| Q94671424 | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
| Q35191908 | Laboratory adaptation of Bordetella pertussis is associated with the loss of type three secretion system functionality |
| Q35026904 | Large-scale label-free quantitative proteomics of the pea aphid-Buchnera symbiosis |
| Q90400965 | Life After Secretion-Yersinia enterocolitica Rapidly Toggles Effector Secretion and Can Resume Cell Division in Response to Changing External Conditions |
| Q39538602 | Living in stools is not as dumb as you think |
| Q40574768 | Lon protease activity causes down-regulation of Salmonella pathogenicity island 1 invasion gene expression after infection of epithelial cells. |
| Q34581241 | Lon, a stress-induced ATP-dependent protease, is critically important for systemic Salmonella enterica serovar typhimurium infection of mice. |
| Q34255633 | Looking deep inside: detection of low-abundance proteins in leaf extracts of Arabidopsis and phloem exudates of pumpkin |
| Q39511017 | Macrophages and epithelial cells respond differently to the Pseudomonas aeruginosa type III secretion system. |
| Q33754588 | Management of Pseudomonas aeruginosa pneumonia: one size does not fit all |
| Q39614560 | Mapping of a YscY binding domain within the LcrH chaperone that is required for regulation of Yersinia type III secretion |
| Q39538062 | Mechanical fractionation reveals structural requirements for enteropathogenic Escherichia coli Tir insertion into host membranes |
| Q24529600 | Mechanisms of protein export across the bacterial outer membrane |
| Q39868407 | Medicinal leech therapy and Aeromonas spp. infection. |
| Q33489891 | Metabolic analysis of the soil microbe Dechloromonas aromatica str. RCB: indications of a surprisingly complex life-style and cryptic anaerobic pathways for aromatic degradation |
| Q35163621 | Metalloprotease NleC suppresses host NF-κB/inflammatory responses by cleaving p65 and interfering with the p65/RPS3 interaction |
| Q33645049 | Microarray Analysis of Response of Salmonella during Infection of HLA-B27- Transfected Human Macrophage-Like U937 Cells |
| Q41871211 | Microarray analysis of the Ler regulon in enteropathogenic and enterohaemorrhagic Escherichia coli strains |
| Q34514415 | Microarray analysis of the osmotic stress response in Pseudomonas aeruginosa |
| Q47138962 | Microbes Tickling Your Tummy: the Importance of the Gut-Brain Axis in Parkinson's Disease |
| Q38647384 | Modelling of the regulation of the hilA promoter of type three secretion system of Salmonella enterica serovar Typhimurium |
| Q29346770 | Modulation of Type III Secretion System in Pseudomonas aeruginosa: Involvement of the PA4857 Gene Product |
| Q33309938 | Modulation of bacterial Type III secretion system by a spermidine transporter dependent signaling pathway |
| Q33768868 | Modulation of host cytoskeleton function by the enteropathogenic Escherichia coli and Citrobacter rodentium effector protein EspG |
| Q64072106 | Molecular Evolution of Type III Secreted Effector Proteins |
| Q33988472 | Molecular and cell biology aspects of plague |
| Q58768402 | Molecular basis for CesT recognition of type III secretion effectors in enteropathogenic Escherichia coli |
| Q29616208 | Molecular basis of bacterial outer membrane permeability revisited |
| Q33558343 | Molecular basis of the interaction of Salmonella with the intestinal mucosa. |
| Q37434696 | Molecular characterization and assembly of the needle complex of the Salmonella typhimurium type III protein secretion system |
| Q42413061 | Molecular characterization and distribution of genes encoding members of the type III effector nleA family among pathogenic Escherichia coli strains |
| Q35695210 | Molecular mechanisms of gastric epithelial cell adhesion and injection of CagA by Helicobacter pylori |
| Q24522458 | Molecular pathogenesis, epidemiology, and clinical manifestations of respiratory infections due to Bordetella pertussis and other Bordetella subspecies |
| Q35280194 | Molecular ruler determines needle length for the Salmonella Spi-1 injectisome. |
| Q37293186 | Molecular signals required for type III secretion and translocation of the Xanthomonas campestris AvrBs2 protein to pepper plants |
| Q39887200 | Molecular typing of, and distribution of genetic markers among, Burkholderia cepacia complex isolates from Brazil. |
| Q21263069 | Moraxella osloensis gene expression in the slug host Deroceras reticulatum |
| Q33557896 | Mouse macrophages are permissive to motile Legionella species that fail to trigger pyroptosis |
| Q33208518 | MucA-mediated coordination of type III secretion and alginate synthesis in Pseudomonas aeruginosa |
| Q30431366 | Multi-Functional Characteristics of the Pseudomonas aeruginosa Type III Needle-Tip Protein, PcrV; Comparison to Orthologs in other Gram-negative Bacteria |
| Q40721285 | Multidrug efflux systems play an important role in the invasiveness of Pseudomonas aeruginosa |
| Q42283500 | Multinucleated giant cell formation and apoptosis in infected host cells is mediated by Burkholderia pseudomallei type III secretion protein BipB. |
| Q36301245 | Multipart Chaperone-Effector Recognition in the Type III Secretion System of Chlamydia trachomatis. |
| Q34976965 | Multiple host kinases contribute to Akt activation during Salmonella infection |
| Q39496612 | Mutagenesis of the Agrobacterium VirE2 single-stranded DNA-binding protein identifies regions required for self-association and interaction with VirE1 and a permissive site for hybrid protein construction |
| Q34316975 | MxiE regulates intracellular expression of factors secreted by the Shigella flexneri 2a type III secretion system |
| Q33997150 | MxiM and MxiJ, base elements of the Mxi-Spa type III secretion system of Shigella, interact with and stabilize the MxiD secretin in the cell envelope |
| Q34618227 | Natural selection drives Drosophila immune system evolution. |
| Q37191809 | Natural selection on the Drosophila antimicrobial immune system |
| Q27664318 | Near-atomic resolution analysis of BipD, a component of the type III secretion system ofBurkholderia pseudomallei |
| Q33664134 | Negative signaling in health and disease. |
| Q39963895 | New protein-protein interactions identified for the regulatory and structural components and substrates of the type III Secretion system of the phytopathogen Xanthomonas axonopodis Pathovar citri. |
| Q92778292 | Nicotiana species as surrogate host for studying the pathogenicity of Acidovorax citrulli, the causal agent of bacterial fruit blotch of cucurbits |
| Q37355875 | Nitrite reductase NirS is required for type III secretion system expression and virulence in the human monocyte cell line THP-1 by Pseudomonas aeruginosa. |
| Q37438837 | Nonhost resistance of tomato to the bean pathogen Pseudomonas syringae pv. syringae B728a is due to a defective E3 ubiquitin ligase domain in avrptobb728a |
| Q39527389 | Nonspecific adherence and fibril biogenesis by Actinobacillus actinomycetemcomitans: TadA protein is an ATPase |
| Q31142460 | NopB, a type III secreted protein of Rhizobium sp. strain NGR234, is associated with pilus-like surface appendages. |
| Q35841646 | NopC Is a Rhizobium-Specific Type 3 Secretion System Effector Secreted by Sinorhizobium (Ensifer) fredii HH103. |
| Q40048925 | Novel Organelles with Elements of Bacterial and Eukaryotic Secretion Systems Weaponize Parasites of Drosophila |
| Q36313508 | Novel candidate virulence factors in rice pathogen Xanthomonas oryzae pv. oryzicola as revealed by mutational analysis |
| Q34853267 | Novel virulence-associated type II secretion system unique to high-pathogenicity Yersinia enterocolitica |
| Q35892099 | Nucleotide sequence and evolution of the five-plasmid complement of the phytopathogen Pseudomonas syringae pv. maculicola ES4326. |
| Q34991119 | O-Antigen Serotypes and Type III Secretory Toxins in Clinical Isolates of Pseudomonas aeruginosa |
| Q39498843 | OmpR regulates the two-component system SsrA-ssrB in Salmonella pathogenicity island 2. |
| Q34558230 | Optimal epitope composition after antigen screening using a live bacterial delivery vector: application to TRP-2. |
| Q35073836 | OspF and OspC1 are Shigella flexneri type III secretion system effectors that are required for postinvasion aspects of virulence |
| Q36421843 | Outer membrane components of the Tad (tight adherence) secreton of Aggregatibacter actinomycetemcomitans |
| Q40942798 | Overexpression of the multidrug efflux pumps MexCD-OprJ and MexEF-OprN is associated with a reduction of type III secretion in Pseudomonas aeruginosa |
| Q49960109 | Pathogen Trojan horse delivers bioactive host protein to alter maize (Zea mays) anther cell behavior in situ. |
| Q34290188 | Pathogenicity islands in bacterial pathogenesis |
| Q34232554 | Pathways leading from BarA/SirA to motility and virulence gene expression in Salmonella. |
| Q24548633 | PcrV immunization enhances survival of burned Pseudomonas aeruginosa-infected mice |
| Q36889954 | Persistent infection with Pseudomonas aeruginosa in ventilator-associated pneumonia |
| Q24562822 | Phages and the evolution of bacterial pathogens: from genomic rearrangements to lysogenic conversion |
| Q31088363 | Phylogenetic analysis of a gene cluster encoding an additional, rhizobial-like type III secretion system that is narrowly distributed among Pseudomonas syringae strains. |
| Q34469628 | Phylogeny of genes for secretion NTPases: identification of the widespread tadA subfamily and development of a diagnostic key for gene classification |
| Q43054516 | Physical characterization of MxiH and PrgI, the needle component of the type III secretion apparatus from Shigella and Salmonella |
| Q35147632 | Physical interaction between RRS1-R, a protein conferring resistance to bacterial wilt, and PopP2, a type III effector targeted to the plant nucleus |
| Q40439695 | Polarity of enteropathogenic Escherichia coli EspA filament assembly and protein secretion |
| Q35623873 | Polyethylene glycol diminishes pathological effects of Citrobacter rodentium infection by blocking bacterial attachment to the colonic epithelia |
| Q35290671 | Polymerization of a single protein of the pathogen Yersinia enterocolitica into needles punctures eukaryotic cells |
| Q33812082 | Polymorphisms in the Pseudomonas aeruginosa type III secretion protein, PcrV - implications for anti-PcrV immunotherapy |
| Q36637903 | Polynucleotide Phosphorylase Regulates Multiple Virulence Factors and the Stabilities of Small RNAs RsmY/Z in Pseudomonas aeruginosa |
| Q35305175 | Potential origins and horizontal transfer of type III secretion systems and effectors |
| Q33995624 | Potential symbiosis-specific genes uncovered by sequencing a 410-kilobase DNA region of the Bradyrhizobium japonicum chromosome |
| Q37560641 | Prediction of bacterial type IV secreted effectors by C-terminal features |
| Q33467383 | Prediction of type III secretion signals in genomes of gram-negative bacteria |
| Q38626784 | Presence of exoY, exoS, exoU and exoT genes, antibiotic resistance and biofilm production among Pseudomonas aeruginosa isolates in Northwest Iran |
| Q33756805 | Presence of genes for type III secretion system 2 in Vibrio mimicus strains |
| Q39455542 | Presence of type III secretion genes in Burkholderia pseudomallei correlates with Ara(-) phenotypes. |
| Q33797791 | Present and future therapeutic strategies for melioidosis and glanders |
| Q35980175 | Process of protein transport by the type III secretion system |
| Q37954303 | Production, secretion and biological activity of Bacillus cereus enterotoxins |
| Q26823960 | Progression of 'OMICS' methodologies for understanding the pathogenicity of Corynebacterium pseudotuberculosis: the Brazilian experience |
| Q38998590 | Protection against Escherichia coli O157:H7 challenge by immunization of mice with purified Tir proteins |
| Q28492902 | Protein binding between PcrG-PcrV and PcrH-PopB/PopD encoded by the pcrGVH-popBD operon of the Pseudomonas aeruginosa type III secretion system |
| Q21563515 | Protein homology network families reveal step-wise diversification of Type III and Type IV secretion systems |
| Q36839222 | Protein secretion and membrane insertion systems in gram-negative bacteria |
| Q88011724 | Protein-Injection Machines in Bacteria |
| Q39741297 | Proteins released by Helicobacter pylori in vitro |
| Q39679978 | Proteolytic cleavage of the FlhB homologue YscU of Yersinia pseudotuberculosis is essential for bacterial survival but not for type III secretion |
| Q36634623 | Proteomic insights into intra- and intercellular plant-bacteria symbiotic association during root nodule formation |
| Q35798768 | Proteomics of protein secretion by Bacillus subtilis: separating the "secrets" of the secretome |
| Q33892913 | Proteomics-based identification of differentially abundant proteins reveals adaptation mechanisms of Xanthomonas citri subsp. citri during Citrus sinensis infection |
| Q27319429 | Pseudomonas aeruginosa ExoT Induces Atypical Anoikis Apoptosis in Target Host Cells by Transforming Crk Adaptor Protein into a Cytotoxin |
| Q34653480 | Pseudomonas aeruginosa cytotoxicity is attenuated at high cell density and associated with the accumulation of phenylacetic acid |
| Q38309387 | Pseudomonas aeruginosa infection of airway epithelial cells modulates expression of Kruppel-like factors 2 and 6 via RsmA-mediated regulation of type III exoenzymes S and Y. |
| Q30478193 | Pseudomonas aeruginosa type III-secreted toxin ExoT inhibits host-cell division by targeting cytokinesis at multiple steps |
| Q35263901 | Pseudomonas and all that |
| Q33988466 | Pseudomonas syringae Hrp type III secretion system and effector proteins. |
| Q35075234 | Pseudomonas syringae HrpJ is a type III secreted protein that is required for plant pathogenesis, injection of effectors, and secretion of the HrpZ1 Harpin |
| Q41439730 | Pseudomonas syringae HrpP Is a type III secretion substrate specificity switch domain protein that is translocated into plant cells but functions atypically for a substrate-switching protein |
| Q36047419 | Pseudomonas syringae naturally lacking the canonical type III secretion system are ubiquitous in nonagricultural habitats, are phylogenetically diverse and can be pathogenic. |
| Q33855521 | Pseudomonas syringae type III chaperones ShcO1, ShcS1, and ShcS2 facilitate translocation of their cognate effectors and can substitute for each other in the secretion of HopO1-1. |
| Q40387827 | Pseudomonas syringae type III secretion system targeting signals and novel effectors studied with a Cya translocation reporter |
| Q28492989 | PtrB of Pseudomonas aeruginosa suppresses the type III secretion system under the stress of DNA damage |
| Q34331657 | Quantification of the physiochemical constraints on the export of spider silk proteins by Salmonella type III secretion |
| Q44478892 | Quantitative proteomic identification of host factors involved in the Salmonella typhimurium infection cycle |
| Q33955457 | Questions about the behaviour of bacterial pathogens in vivo |
| Q34351491 | Quorum sensing regulates type III secretion in Vibrio harveyi and Vibrio parahaemolyticus |
| Q36052613 | RNA-Seq Analysis of Differential Gene Expression Responding to Different Rhizobium Strains in Soybean (Glycine max) Roots |
| Q37627811 | RNA-Seq analysis of nodule development at five different developmental stages of soybean (Glycine max) inoculated with Bradyrhizobium japonicum strain 113-2. |
| Q36651548 | Rapid mobilization of membrane lipids in wheat leaf sheaths during incompatible interactions with Hessian fly. |
| Q41815584 | Real-time reverse transcription-PCR for transcriptional expression analysis of virulence and housekeeping genes in viable but nonculturable Vibrio parahaemolyticus after recovery of culturability |
| Q36559367 | Reciprocal secretion of proteins by the bacterial type III machines of plant and animal pathogens suggests universal recognition of mRNA targeting signals |
| Q30358493 | Recombinant Salmonella Bacteria Vectoring HIV/AIDS Vaccines. |
| Q34435137 | Recombination in the genome of Chlamydia trachomatis involving the polymorphic membrane protein C gene relative to ompA and evidence for horizontal gene transfer |
| Q34433420 | Reconceptualizing the chlamydial inclusion as a pathogen-specified parasitic organelle: an expanded role for Inc proteins |
| Q44511177 | Regulation of Arabidopsis COPINE 1 gene expression in response to pathogens and abiotic stimuli |
| Q39158295 | Regulation of Rab5 function during phagocytosis of live Pseudomonas aeruginosa in macrophages |
| Q33883450 | Regulation of a type III and a putative secretion system in Edwardsiella tarda by EsrC is under the control of a two-component system, EsrA-EsrB |
| Q34775540 | Regulation of type III secretion system 1 gene expression in Vibrio parahaemolyticus is dependent on interactions between ExsA, ExsC, and ExsD |
| Q40422063 | Regulators encoded in the Escherichia coli type III secretion system 2 gene cluster influence expression of genes within the locus for enterocyte effacement in enterohemorrhagic E. coli O157:H7. |
| Q28493109 | Regulatory role of PopN and its interacting partners in type III secretion of Pseudomonas aeruginosa |
| Q34320687 | Requirement of flhA for swarming differentiation, flagellin export, and secretion of virulence-associated proteins in Bacillus thuringiensis |
| Q34484355 | Rhizobium-legume symbiosis in the absence of Nod factors: two possible scenarios with or without the T3SS |
| Q36363508 | Role of EscP (Orf16) in injectisome biogenesis and regulation of type III protein secretion in enteropathogenic Escherichia coli |
| Q34975645 | Role of Escherichia coli O157:H7 virulence factors in colonization at the bovine terminal rectal mucosa |
| Q39538800 | Role of FliJ in flagellar protein export in Salmonella |
| Q34740089 | Role of Salmonella Pathogenicity Island 1 protein IacP in Salmonella enterica serovar typhimurium pathogenesis |
| Q30827325 | Role of flagella in host cell invasion by Burkholderia cepacia |
| Q33769194 | Role of predicted transmembrane domains for type III translocation, pore formation, and signaling by the Yersinia pseudotuberculosis YopB protein |
| Q36437411 | Role of the Hrp type III protein secretion system in growth of Pseudomonas syringae pv. syringae B728a on host plants in the field. |
| Q40173901 | Role of the Salmonella pathogenicity island 1 (SPI-1) protein InvB in type III secretion of SopE and SopE2, two Salmonella effector proteins encoded outside of SPI-1. |
| Q24627445 | Role of the inflammasome, IL-1β, and IL-18 in bacterial infections |
| Q39247048 | Role of the pilot protein YscW in the biogenesis of the YscC secretin in Yersinia enterocolitica |
| Q33716024 | Role of the type III secreted exoenzymes S, T, and Y in systemic spread of Pseudomonas aeruginosa PAO1 in vivo |
| Q40124075 | Salicylidene acylhydrazides that affect type III protein secretion in Salmonella enterica serovar typhimurium |
| Q35917486 | Salmonella Engages Host MicroRNAs To Modulate SUMOylation: a New Arsenal for Intracellular Survival |
| Q92715663 | Salmonella Pathogenicity Island 1 (SPI-1) and Its Complex Regulatory Network |
| Q58321342 | Salmonella SipA mimics a cognate SNARE for host Syntaxin8 to promote fusion with early endosomes |
| Q37915291 | Salmonella and Caspase-1: A complex Interplay of Detection and Evasion |
| Q36054725 | Salmonella effectors: important players modulating host cell function during infection |
| Q39521867 | Salmonella enterica serovar Gallinarum requires the Salmonella pathogenicity island 2 type III secretion system but not the Salmonella pathogenicity island 1 type III secretion system for virulence in chickens |
| Q35785051 | Salmonella enterica serovar enteritidis modulates intestinal epithelial miR-128 levels to decrease macrophage recruitment via macrophage colony-stimulating factor |
| Q41976795 | Salmonella enterica serovar enteritidis pathogenicity island 1 is not essential for but facilitates rapid systemic spread in chickens. |
| Q36933192 | Salmonella enterica serovar gallinarum requires ppGpp for internalization and survival in animal cells |
| Q34005208 | Salmonella enterica serovar typhimurium invasion is repressed in the presence of bile |
| Q39503254 | Salmonella host cell invasion emerged by acquisition of a mosaic of separate genetic elements, including Salmonella pathogenicity island 1 (SPI1), SPI5, and sopE2. |
| Q35114802 | Salmonella maintains the integrity of its intracellular vacuole through the action of SifA. |
| Q33859408 | Salmonella pathogenesis and processing of secreted effectors by caspase-3 |
| Q24811102 | Salmonella pathogenicity island 2 is expressed prior to penetrating the intestine |
| Q36370147 | Salmonella pathogenicity island 2 mediates protection of intracellular Salmonella from reactive nitrogen intermediates |
| Q28490019 | Salmonella pathogenicity island 2-encoded proteins SseC and SseD are essential for virulence and are substrates of the type III secretion system |
| Q33559019 | Salmonella pathogenicity island 2-mediated overexpression of chimeric SspH2 proteins for simultaneous induction of antigen-specific CD4 and CD8 T cells |
| Q30480354 | Salmonella trafficking is defined by continuous dynamic interactions with the endolysosomal system. |
| Q34317570 | Salmonella type III secretion-associated protein InvE controls translocation of effector proteins into host cells |
| Q35128691 | Salmonella typhimurium disseminates within its host by manipulating the motility of infected cells |
| Q40994584 | Salmonella-induced filament formation is a dynamic phenotype induced by rapidly replicating Salmonella enterica serovar typhimurium in epithelial cells. |
| Q39573966 | Secreted effector proteins of Salmonella dublin act in concert to induce enteritis |
| Q39755036 | Secretin of the enteropathogenic Escherichia coli type III secretion system requires components of the type III apparatus for assembly and localization |
| Q39694948 | Secretion of alpha-amylase from Pseudoalteromonas haloplanktis TAB23: two different pathways in different hosts |
| Q39982385 | Secretion of theorgCGene Product bySalmonella entericaSerovar Typhimurium |
| Q33883322 | SepZ/EspZ is secreted and translocated into HeLa cells by the enteropathogenic Escherichia coli type III secretion system |
| Q37841621 | Sequencing and characterizing the genome of Estrella lausannensis as an undergraduate project: training students and biological insights |
| Q39678365 | Shigella Spa32 is an essential secretory protein for functional type III secretion machinery and uniformity of its needle length |
| Q42633978 | Shigella flexneri phagosomal escape is independent of invasion. |
| Q27687005 | Shigella: a model of virulence regulation in vivo |
| Q39502586 | SigE is a chaperone for the Salmonella enterica serovar Typhimurium invasion protein SigD. |
| Q38653229 | Signaling requirements for Erwinia amylovora-induced disease resistance, callose deposition, and cell growth in the nonhost Arabidopsis thaliana. |
| Q36313567 | Signature-tagged mutagenesis of Edwardsiella ictaluri identifies virulence-related genes, including a salmonella pathogenicity island 2 class of type III secretion systems |
| Q40467826 | Simple and reliable method to precipitate proteins from bacterial culture supernatant |
| Q40079180 | Single-domain antibodies pinpoint potential targets within Shigella invasion plasmid antigen D of the needle tip complex for inhibition of type III secretion |
| Q35636329 | Single-nucleotide-polymorphism mapping of the Pseudomonas aeruginosa type III secretion toxins for development of a diagnostic multiplex PCR system |
| Q57476150 | SipA mimics a cognate SNARE for host Syntaxin8 to promote fusion with early endosomes |
| Q34120333 | Site-specific proteolysis of the MALP-404 lipoprotein determines the release of a soluble selective lipoprotein-associated motif-containing fragment and alteration of the surface phenotype of Mycoplasma fermentans |
| Q33768953 | Small-molecule inhibitors specifically targeting type III secretion |
| Q35201897 | Snapshots of usher-mediated protein secretion and ordered pilus assembly |
| Q34010367 | Sodium ion cycle in bacterial pathogens: evidence from cross-genome comparisons |
| Q36955978 | Soybean seed extracts preferentially express genomic loci of Bradyrhizobium japonicum in the initial interaction with soybean, Glycine max (L.) Merr. |
| Q34314419 | Spa32 regulates a switch in substrate specificity of the type III secreton of Shigella flexneri from needle components to Ipa proteins |
| Q34006737 | Spa33, a cell surface-associated subunit of the Mxi-Spa type III secretory pathway of Shigella flexneri, regulates Ipa protein traffic |
| Q33313651 | Spatial constraints within the chlamydial host cell inclusion predict interrupted development and persistence |
| Q34318039 | SpiC is required for translocation of Salmonella pathogenicity island 2 effectors and secretion of translocon proteins SseB and SseC |
| Q36155240 | SrfJ, a Salmonella type III secretion system effector regulated by PhoP, RcsB, and IolR. |
| Q57048274 | SsaV Interacts with SsaL to Control the Translocon-to-Effector Switch in the SPI-2 Type Three Secretion System |
| Q28490029 | SseBCD proteins are secreted by the type III secretion system of Salmonella pathogenicity island 2 and function as a translocon |
| Q34033443 | SseJ deacylase activity by Salmonella enterica serovar Typhimurium promotes virulence in mice |
| Q37521628 | SseK1 and SseK2 are novel translocated proteins of Salmonella enterica serovar typhimurium. |
| Q33431015 | Statistical characterization of the GxxxG glycine repeats in the flagellar biosynthesis protein FliH and its Type III secretion homologue YscL |
| Q24683633 | Stepwise formation of the bacterial flagellar system |
| Q35173801 | Strategies for Intracellular Survival of Burkholderia pseudomallei. |
| Q36105372 | Striking a balance: modulation of the actin cytoskeleton by Salmonella |
| Q27664835 | Structural Basis for the Secretion of EvpC: A Key Type VI Secretion System Protein from Edwardsiella tarda |
| Q27677661 | Structural Characterisation of Tpx from Yersinia pseudotuberculosis Reveals Insights into the Binding of Salicylidene Acylhydrazide Compounds |
| Q92498892 | Structural analysis of ligand-bound states of the Salmonella type III secretion system ATPase InvC |
| Q39730227 | Structural characterization of the N terminus of IpaC from Shigella flexneri |
| Q54360365 | Structural insights on two hypothetical secretion chaperones from Xanthomonas axonopodis pv. citri. |
| Q35279783 | Structure and electrophysiological properties of the YscC secretin from the type III secretion system of Yersinia enterocolitica |
| Q27680527 | Structure of CT584 fromChlamydia trachomatisrefined to 3.05 Å resolution |
| Q27642850 | Structure of HrcQB-C, a conserved component of the bacterial type III secretion systems |
| Q40101906 | Structure of Spa15, a type III secretion chaperone from Shigella flexneri with broad specificity |
| Q42237643 | Structure of a pathogenic type 3 secretion system in action |
| Q27661313 | Structure of the Cytoplasmic Domain of the Flagellar Secretion Apparatus Component FlhA from Helicobacter pylori |
| Q27677358 | Structure of the cytoplasmic domain ofYersinia pestisYscD, an essential component of the type III secretion system |
| Q24549290 | Structures of gram-negative cell walls and their derived membrane vesicles |
| Q33995607 | Subset of hybrid eukaryotic proteins is exported by the type I secretion system of Erwinia chrysanthemi |
| Q38433985 | Subtractive Protein Profiling of Salmonella typhimurium Biofilm Treated with DMSO. |
| Q35028331 | SuhB is a regulator of multiple virulence genes and essential for pathogenesis of Pseudomonas aeruginosa |
| Q33944789 | Supermolecular structure of the enteropathogenic Escherichia coli type III secretion system and its direct interaction with the EspA-sheath-like structure |
| Q40392389 | Supramolecular structure of the Shigella type III secretion machinery: the needle part is changeable in length and essential for delivery of effectors |
| Q35913097 | Swarming behavior of and hemolysin BL secretion by Bacillus cereus. |
| Q36747816 | Symbiosis-promoting and deleterious effects of NopT, a novel type 3 effector of Rhizobium sp. strain NGR234. |
| Q51777866 | Symbiotic use of pathogenic strategies: rhizobial protein secretion systems. |
| Q29346673 | Synergistic activation of the pathogenicity-related proline iminopeptidase gene in Xanthomonas campestris pv. campestris by HrpX and a LuxR homolog |
| Q33994669 | Synergistic hydrolysis of carboxymethyl cellulose and acid-swollen cellulose by two endoglucanases (CelZ and CelY) from Erwinia chrysanthemi |
| Q39741669 | Synergistic protection of mice against plague with monoclonal antibodies specific for the F1 and V antigens of Yersinia pestis |
| Q60958565 | Synonymous Codon Usages as an Evolutionary Dynamic for |
| Q33639942 | Synthesis of 2-(2-aminopyrimidine)-2,2-difluoroethanols as potential bioisosters of salicylidene acylhydrazides. |
| Q33704909 | Synthesis of [4-(2-hydroxyphenyl)thiazol-2-yl]methanones as potential bioisosteres of salicylidene acylhydrazides. |
| Q33269622 | Systematic analysis of the regulation of type three secreted effectors in Salmonella enterica serovar Typhimurium. |
| Q21284314 | T3DB: an integrated database for bacterial type III secretion system |
| Q55017646 | T3SS effectors in Vibrios: Homology in sequence, diversity in biological functions? |
| Q34614765 | T3_MM: a Markov model effectively classifies bacterial type III secretion signals. |
| Q24805246 | TLR4 signaling is essential for survival in acute lung injury induced by virulent Pseudomonas aeruginosa secreting type III secretory toxins |
| Q28240172 | TLR5 and Ipaf: dual sensors of bacterial flagellin in the innate immune system |
| Q92557925 | Tanshinones: First-in-Class Inhibitors of the Biogenesis of the Type 3 Secretion System Needle of Pseudomonas aeruginosa for Antibiotic Therapy |
| Q28902456 | Tarp regulates early Chlamydia-induced host cell survival through interactions with the human adaptor protein SHC1 |
| Q34935390 | Temporal Expression of Type III Secretion Genes of Chlamydia pneumoniae |
| Q33260347 | Terminal reassortment drives the quantum evolution of type III effectors in bacterial pathogens |
| Q40582422 | The ADP ribosyltransferase domain of Pseudomonas aeruginosa ExoT contributes to its biological activities. |
| Q39775119 | The ATPase FliI can interact with the type III flagellar protein export apparatus in the absence of its regulator, FliH. |
| Q33993163 | The Agrobacterium tumefaciens chaperone-like protein, VirE1, interacts with VirE2 at domains required for single-stranded DNA binding and cooperative interaction. |
| Q35625648 | The Arabidopsis thaliana-pseudomonas syringae interaction |
| Q37643836 | The Bordetella bronchiseptica type III secretion system is required for persistence and disease severity but not transmission in swine |
| Q34010148 | The Brucella suis virB operon is induced intracellularly in macrophages |
| Q28730662 | The Chlamydia psittaci genome: a comparative analysis of intracellular pathogens |
| Q35075114 | The Chlamydial Type III Secretion Mechanism: Revealing Cracks in a Tough Nut. |
| Q36575276 | The DnaK/DnaJ chaperone machinery of Salmonella enterica serovar Typhimurium is essential for invasion of epithelial cells and survival within macrophages, leading to systemic infection |
| Q34083176 | The DotA protein from Legionella pneumophila is secreted by a novel process that requires the Dot/Icm transporter |
| Q33889316 | The EHEC type III effector NleL is an E3 ubiquitin ligase that modulates pedestal formation |
| Q34148431 | The ETT2 gene cluster, encoding a second type III secretion system from Escherichia coli, is present in the majority of strains but has undergone widespread mutational attrition |
| Q37615104 | The Ecological Role of Type Three Secretion Systems in the Interaction of Bacteria with Fungi in Soil and Related Habitats Is Diverse and Context-Dependent |
| Q30168706 | The Haemophilus influenzae Hia adhesin is an autotransporter protein that remains uncleaved at the C terminus and fully cell associated |
| Q39698949 | The Helicobacter pylori CagA protein induces cortactin dephosphorylation and actin rearrangement by c-Src inactivation |
| Q39644861 | The Hrp pilus of Pseudomonas syringae elongates from its tip and acts as a conduit for translocation of the effector protein HrpZ. |
| Q30502008 | The LC3 recruitment mechanism is separate from Atg9L1-dependent membrane formation in the autophagic response against Salmonella |
| Q30313661 | The Predicted Lytic Transglycosylase HpaH from Xanthomonas campestris pv. vesicatoria Associates with the Type III Secretion System and Promotes Effector Protein Translocation |
| Q37568779 | The Pseudomonas aeruginosa Type III secretion system plays a dual role in the regulation of caspase-1 mediated IL-1beta maturation. |
| Q36109469 | The Pseudomonas aeruginosa type III secretion system has an exotoxin S/T/Y independent pathogenic role during acute lung infection |
| Q34149353 | The Pseudomonas syringae HopPtoV protein is secreted in culture and translocated into plant cells via the type III protein secretion system in a manner dependent on the ShcV type III chaperone |
| Q35699642 | The Pseudomonas syringae Hrp pathogenicity island has a tripartite mosaic structure composed of a cluster of type III secretion genes bounded by exchangeable effector and conserved effector loci that contribute to parasitic fitness and pathogenicity |
| Q64273419 | The Role of Proteases in the Virulence of Plant Pathogenic Bacteria |
| Q37713164 | The Salmonella Spi1 virulence regulatory protein HilD directly activates transcription of the flagellar master operon flhDC. |
| Q34522155 | The Salmonella enterica serovar typhimurium translocated effectors SseJ and SifB are targeted to the Salmonella-containing vacuole. |
| Q34048081 | The Shigella flexneri effector OspG interferes with innate immune responses by targeting ubiquitin-conjugating enzymes |
| Q28073674 | The Structure and Function of Type III Secretion Systems |
| Q36557376 | The SycN/YscB chaperone-binding domain of YopN is required for the calcium-dependent regulation of Yop secretion by Yersinia pestis |
| Q45949107 | The TAL Effector AvrBs3 from Xanthomonas campestris pv. vesicatoria Contains Multiple Export Signals and Can Enter Plant Cells in the Absence of the Type III Secretion Translocon. |
| Q47281616 | The Vibrio alginolyticus T3SS effectors, Val1686 and Val1680, induce cell rounding, apoptosis and lysis of fish epithelial cells. |
| Q35604617 | The Xanthomonas Hrp type III system secretes proteins from plant and mammalian bacterial pathogens |
| Q24792258 | The Yersinia YopE and YopH type III effector proteins enhance bacterial proliferation following contact with eukaryotic cells |
| Q33738622 | The Yersinia deadly kiss. |
| Q33601522 | The Yersinia pestis YscY protein directly binds YscX, a secreted component of the type III secretion machinery |
| Q40909327 | The YopD translocator of Yersinia pseudotuberculosis is a multifunctional protein comprised of discrete domains. |
| Q40264288 | The animal pathogen-like type III secretion system is required for the intracellular survival of Burkholderia mallei within J774.2 macrophages |
| Q35584872 | The bacterial adaptive response gene, barA, encodes a novel conserved histidine kinase regulatory switch for adaptation and modulation of metabolism in Escherichia coli |
| Q37993038 | The blueprint of the type-3 injectisome |
| Q36483692 | The chaperone IpgC copurifies with the virulence regulator MxiE |
| Q33640294 | The conserved Tarp actin binding domain is important for chlamydial invasion |
| Q35671636 | The deubiquitinase activity of the Salmonella pathogenicity island 2 effector, SseL, prevents accumulation of cellular lipid droplets |
| Q35113241 | The effect of cell growth phase on the regulatory cross-talk between flagellar and Spi1 virulence gene expression |
| Q33994411 | The flagellar hook protein, FlgE, of Salmonella enterica serovar typhimurium is posttranscriptionally regulated in response to the stage of flagellar assembly |
| Q35052377 | The gene coding for the Hrp pilus structural protein is required for type III secretion of Hrp and Avr proteins in Pseudomonas syringae pv. tomato |
| Q43121875 | The global virulence regulator PhcA negatively controls the Ralstonia solanacearum hrp regulatory cascade by repressing expression of the PrhIR signaling proteins |
| Q34864770 | The hierarchy quorum sensing network in Pseudomonas aeruginosa |
| Q34109059 | The insect endosymbiont Sodalis glossinidius utilizes a type III secretion system for cell invasion |
| Q34004916 | The locus of enterocyte effacement (LEE)-encoded regulator controls expression of both LEE- and non-LEE-encoded virulence factors in enteropathogenic and enterohemorrhagic Escherichia coli. |
| Q42704912 | The locus of enterocyte effacement-encoded effector proteins all promote enterohemorrhagic Escherichia coli pathogenicity in infant rabbits |
| Q36858588 | The main Aeromonas pathogenic factors |
| Q34598830 | The metabolic enzyme AdhE controls the virulence of Escherichia coli O157:H7 |
| Q34711734 | The molecular mechanism of acute lung injury caused by Pseudomonas aeruginosa: from bacterial pathogenesis to host response |
| Q24548840 | The mxi-Spa type III secretory pathway of Shigella flexneri requires an outer membrane lipoprotein, MxiM, for invasin translocation |
| Q28276177 | The non-flagellar type III secretion system evolved from the bacterial flagellum and diversified into host-cell adapted systems |
| Q33955468 | The pathogenesis of Shigella flexneri infection: lessons from in vitro and in vivo studies |
| Q28476204 | The pathogenic properties of a novel and conserved gene product, KerV, in proteobacteria |
| Q34144685 | The players in a mutualistic symbiosis: insects, bacteria, viruses, and virulence genes |
| Q21132404 | The resveratrol tetramer (-)-hopeaphenol inhibits type III secretion in the gram-negative pathogens Yersinia pseudotuberculosis and Pseudomonas aeruginosa |
| Q41296181 | The rhizobacterial elicitor acetoin induces systemic resistance in Arabidopsis thaliana |
| Q40182759 | The salicylidene acylhydrazide INP0341 attenuates Pseudomonas aeruginosa virulence in vitro and in vivo |
| Q42021486 | The transiently ordered regions in intrinsically disordered ExsE are correlated with structural elements involved in chaperone binding. |
| Q33878820 | The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes |
| Q34759935 | The two murein lipoproteins of Salmonella enterica serovar Typhimurium contribute to the virulence of the organism |
| Q41475300 | The type III pseudomonal exotoxin U activates the c-Jun NH2-terminal kinase pathway and increases human epithelial interleukin-8 production |
| Q42569269 | The type III secretion system and cytotoxic enterotoxin alter the virulence of Aeromonas hydrophila |
| Q41985909 | Three-Axis Model for Atg Recruitment in Autophagy against Salmonella |
| Q39518033 | Tir tyrosine phosphorylation and pedestal formation are delayed in enteropathogenic Escherichia coli sepZ::TnphoA mutant 30-5-1(3). |
| Q54856298 | Total Synthesis of the Resveratrol Oligomers (±)‐Ampelopsin B and (±)‐ϵ‐Viniferin. |
| Q33375185 | Toxicogenomic response of Pseudomonas aeruginosa to ortho-phenylphenol |
| Q37954297 | Toxins and secretion systems of Photorhabdus luminescens |
| Q26783635 | Trachoma and Ocular Chlamydial Infection in the Era of Genomics |
| Q34306223 | Transcription of the SsrAB regulon is repressed by alkaline pH and is independent of PhoPQ and magnesium concentration |
| Q38332702 | Transcriptional adaptation of Shigella flexneri during infection of macrophages and epithelial cells: insights into the strategies of a cytosolic bacterial pathogen |
| Q34697291 | Transcriptional and translational control of the Salmonella fliC gene |
| Q33224085 | Transcriptional inhibitor of virulence factors in enteropathogenic Escherichia coli. |
| Q33517975 | Transcriptional profile of Pseudomonas syringae pv. phaseolicola NPS3121 in response to tissue extracts from a susceptible Phaseolus vulgaris L. cultivar |
| Q38337507 | Transcriptome of enterohemorrhagic Escherichia coli O157 adhering to eukaryotic plasma membranes |
| Q35099063 | Treatment of Chlamydia trachomatis with a small molecule inhibitor of the Yersinia type III secretion system disrupts progression of the chlamydial developmental cycle |
| Q37405909 | TtsI regulates symbiotic genes in Rhizobium species NGR234 by binding to tts boxes |
| Q36923034 | Two-dimensional gel electrophoresis in bacterial proteomics |
| Q36747877 | Type II secretory pathway for surface secretion of DraD invasin from the uropathogenic Escherichia coli Dr+ strain. |
| Q97423517 | Type III Secretion 1 Effector Gene Diversity Among Vibrio Isolates From Coastal Areas in China |
| Q39645093 | Type III secretion chaperone-dependent regulation: activation of virulence genes by SicA and InvF in Salmonella typhimurium. |
| Q30403849 | Type III secretion is essential for the rapidly fatal diarrheal disease caused by non-O1, non-O139 Vibrio cholerae. |
| Q39654226 | Type III secretion of Salmonella enterica serovar Typhimurium translocated effectors and SseFG. |
| Q41908827 | Type III secretion of the Salmonella effector protein SopE is mediated via an N-terminal amino acid signal and not an mRNA sequence |
| Q24793790 | Type III secretion proteins PcrV and PcrG from Pseudomonas aeruginosa form a 1:1 complex through high affinity interactions |
| Q37029472 | Type III secretion system 1 genes in Vibrio parahaemolyticus are positively regulated by ExsA and negatively regulated by ExsD. |
| Q40638415 | Type III secretion system genes in clinical Aeromonas isolates. |
| Q34865653 | Type III secretion systems and bacterial flagella: insights into their function from structural similarities |
| Q34156206 | Type III secretion systems and the evolution of mutualistic endosymbiosis |
| Q38586932 | Type III secretion systems: the bacterial flagellum and the injectisome |
| Q39512479 | Type III secretion-dependent hemolytic activity of enteropathogenic Escherichia coli |
| Q35550224 | Type III secretion: a virulence factor delivery system essential for the pathogenicity of Burkholderia mallei. |
| Q28074332 | Type Three Secretion System in Attaching and Effacing Pathogens |
| Q33559645 | Type V protein secretion pathway: the autotransporter story |
| Q89950008 | Type three secretion system in Salmonella Typhimurium: the key to infection |
| Q47596357 | Type-III secretion pore formed by flagellar protein FliP. |
| Q35015052 | Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation |
| Q33843502 | Tyrosine-phosphorylated bacterial proteins: Trojan horses for the host cell |
| Q34751865 | Ubiquity of putative type III secretion genes among clinical and environmental Burkholderia pseudomallei isolates in Northern Australia |
| Q36156270 | Unraveling the secret lives of bacteria: use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression |
| Q40548064 | Uptake and replication of Salmonella enterica in Acanthamoeba rhysodes |
| Q24682662 | Use of the Galleria mellonella Caterpillar as a Model Host To Study the Role of the Type III Secretion System in Pseudomonas aeruginosa Pathogenesis |
| Q61800019 | Vaccine-Induced Protection Against Furunculosis Involves Pre-emptive Priming of Humoral Immunity in Arctic Charr |
| Q34434286 | Variation in the effectors of the type III secretion system among Photorhabdus species as revealed by genomic analysis |
| Q33715983 | Vibrio parahaemolyticus disruption of epithelial cell tight junctions occurs independently of toxin production. |
| Q33994490 | VirB6 is required for stabilization of VirB5 and VirB3 and formation of VirB7 homodimers in Agrobacterium tumefaciens |
| Q88766625 | Virulence Factors in Salmonella Typhimurium: The Sagacity of a Bacterium |
| Q34006158 | Virulence functions of autotransporter proteins |
| Q35176257 | Virulence of enteropathogenic Escherichia coli, a global pathogen |
| Q34005823 | Virulence plasmid of Rhodococcus equi contains inducible gene family encoding secreted proteins |
| Q33964205 | Vp1659 is a Vibrio parahaemolyticus type III secretion system 1 protein that contributes to translocation of effector proteins needed to induce cytolysis, autophagy, and disruption of actin structure in HeLa cells |
| Q58805113 | Whole Genome Analyses Suggests that sensu lato Contains Two Additional Novel Genera ( gen. nov., and gen. nov.): Implications for the Evolution of Diazotrophy and Nodulation in the |
| Q21559505 | Yersinia controls type III effector delivery into host cells by modulating Rho activity |
| Q37283839 | Yersinia enterocolitica targets cells of the innate and adaptive immune system by injection of Yops in a mouse infection model. |
| Q40936347 | Yersinia enterocolitica type III secretion depends on the proton motive force but not on the flagellar motor components MotA and MotB |
| Q41441370 | Yersinia enterocolitica type III secretion of YopR requires a structure in its mRNA |
| Q34320096 | Yersinia enterocolitica type III secretion: yscM1 and yscM2 regulate yop gene expression by a posttranscriptional mechanism that targets the 5' untranslated region of yop mRNA. |
| Q39516968 | Yersinia pestis YscG protein is a Syc-like chaperone that directly binds yscE. |
| Q21146740 | YersiniaBase: a genomic resource and analysis platform for comparative analysis of Yersinia |
| Q39678327 | YopD and LcrH regulate expression of Yersinia enterocolitica YopQ by a posttranscriptional mechanism and bind to yopQ RNA. |
| Q39678306 | YplA is exported by the Ysc, Ysa, and flagellar type III secretion systems of Yersinia enterocolitica |
| Q34810031 | YscP and YscU regulate substrate specificity of the Yersinia type III secretion system |
| Q39758533 | YscP and YscU switch the substrate specificity of the Yersinia type III secretion system by regulating export of the inner rod protein YscI. |
| Q28492821 | YscP of Yersinia pestis is a secreted component of the Yop secretion system |
| Q36513832 | YscU cleavage and the assembly of Yersinia type III secretion machine complexes |
| Q41441221 | YtxR acts as an overriding transcriptional off switch for the Yersinia enterocolitica Ysc-Yop type 3 secretion system |
| Q35013143 | c-Jun NH2-terminal kinase-mediated signaling is essential for Pseudomonas aeruginosa ExoS-induced apoptosis |
| Q40403154 | coliBASE: an online database for Escherichia coli, Shigella and Salmonella comparative genomics. |
| Q35900007 | iTRAQ-based proteomic profiling of Vibrio parahaemolyticus under various culture conditions |
| Q33877186 | vttRA and vttRB Encode ToxR family proteins that mediate bile-induced expression of type three secretion system genes in a non-O1/non-O139 Vibrio cholerae strain |
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