| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0966-842X(02)02451-4 |
| P698 | PubMed publication ID | 12377556 |
| P50 | author | Magdalen Lindeberg | Q57219292 |
| David J. Schneider | Q30517968 | ||
| P2093 | author name string | Alan Collmer | |
| James R Alfano | |||
| Tanja Petnicki-Ocwieja | |||
| P2860 | cites work | Comparison of the genomes of two Xanthomonas pathogens with differing host specificities | Q22122346 |
| Genome sequence of the plant pathogen Ralstonia solanacearum | Q22122347 | ||
| Genomewide identification of proteins secreted by the Hrp type III protein secretion system of Pseudomonas syringae pv. tomato DC3000 | Q24530644 | ||
| Pseudomonas aeruginosa ExoT acts in vivo as a GTPase-activating protein for RhoA, Rac1, and Cdc42. | Q39654456 | ||
| YplA is exported by the Ysc, Ysa, and flagellar type III secretion systems of Yersinia enterocolitica | Q39678306 | ||
| The Pseudomonas syringae Hrp regulation and secretion system controls the production and secretion of multiple extracellular proteins | Q39843369 | ||
| 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 | ||
| A single promoter sequence recognized by a newly identified alternate sigma factor directs expression of pathogenicity and host range determinants in Pseudomonas syringae | Q39931999 | ||
| Cultivar-specific avirulence and virulence functions assigned to avrPphF in Pseudomonas syringae pv. phaseolicola, the cause of bean halo-blight disease. | Q40430057 | ||
| Disruption of signaling by Yersinia effector YopJ, a ubiquitin-like protein protease. | Q40840610 | ||
| A Yersinia effector and a Pseudomonas avirulence protein define a family of cysteine proteases functioning in bacterial pathogenesis. | Q41471661 | ||
| Molecular characterization of type III secretion signals via analysis of synthetic N-terminal amino acid sequences | Q41472978 | ||
| Targeting exported substrates to the Yersinia TTSS: different functions for different signals? | Q41475240 | ||
| Translocation of a hybrid YopE-adenylate cyclase from Yersinia enterocolitica into HeLa cells | Q41497627 | ||
| Characterization of the Pseudomonas syringae pv. tomato AvrRpt2 protein: demonstration of secretion and processing during bacterial pathogenesis | Q41670828 | ||
| RIN4 interacts with Pseudomonas syringae type III effector molecules and is required for RPM1-mediated resistance in Arabidopsis | Q42520168 | ||
| The virulence plasmid pWR100 and the repertoire of proteins secreted by the type III secretion apparatus of Shigella flexneri | Q42638971 | ||
| A functional screen for the type III (Hrp) secretome of the plant pathogen Pseudomonas syringae. | Q42671228 | ||
| ADP ribosylation of Arg41 of Rap by ExoS inhibits the ability of Rap to interact with its guanine nucleotide exchange factor, C3G. | Q43547714 | ||
| An abundance of bacterial ADP-ribosyltransferases--implications for the origin of exotoxins and their human homologues | Q43660256 | ||
| Two distinct Pseudomonas effector proteins interact with the Pto kinase and activate plant immunity | Q44025701 | ||
| Identification of Pseudomonas syringae pv. tomato genes induced during infection of Arabidopsis thaliana. | Q44463240 | ||
| Characterization of avrE from Pseudomonas syringae pv. tomato: a hrp-linked avirulence locus consisting of at least two transcriptional units. | Q48076249 | ||
| The hrpRS locus of Pseudomonas syringae pv. phaseolicola constitutes a complex regulatory unit | Q48076320 | ||
| Pseudomonas syringae pv. syringae harpinPss: a protein that is secreted via the Hrp pathway and elicits the hypersensitive response in plants | Q48111472 | ||
| Salmonella SsrB activates a global regulon of horizontally acquired genes. | Q50120790 | ||
| The pseudomonas AvrPto protein is differentially recognized by tomato and tobacco and is localized to the plant plasma membrane. | Q52541964 | ||
| Eukaryotic Fatty Acylation Drives Plasma Membrane Targeting and Enhances Function of Several Type III Effector Proteins from Pseudomonas syringae | Q57266282 | ||
| Role of the Hrp pilus in type III protein secretion in Pseudomonas syringae | Q64449530 | ||
| Molecular secrets of bacterial type III effector proteins | Q28190618 | ||
| Plant pathogens and integrated defence responses to infection | Q28207107 | ||
| A harpin binding site in tobacco plasma membranes mediates activation of the pathogenesis-related gene HIN1 independent of extracellular calcium but dependent on mitogen-activated protein kinase activity | Q28364429 | ||
| Exoenzyme S of Pseudomonas aeruginosa is secreted by a type III pathway | Q28492720 | ||
| The Salmonella invasin SipB induces macrophage apoptosis by binding to caspase-1 | Q28512341 | ||
| Identification of novel hrp-regulated genes through functional genomic analysis of the Pseudomonas syringae pv. tomato DC3000 genome | Q29346742 | ||
| Functional analysis of HrpF, a putative type III translocon protein from Xanthomonas campestris pv. vesicatoria | Q30320829 | ||
| Port of entry--the type III secretion translocon | Q30320840 | ||
| cDNA-AFLP analysis unravels a genome-wide hrpG-regulon in the plant pathogen Xanthomonas campestris pv. vesicatoria | Q30320916 | ||
| Cloned avirulence genes from the tomato pathogen Pseudomonas syringae pv. tomato confer cultivar specificity on soybean | Q33238226 | ||
| Cloned avirulence gene of Pseudomonas syringae pv. glycinea determines race-specific incompatibility on Glycine max (L.) Merr | Q33238784 | ||
| Regulation of type III secretion systems | Q33337072 | ||
| Type III secretion machines: bacterial devices for protein delivery into host cells | Q33639326 | ||
| Enhancer-binding proteins HrpR and HrpS interact to regulate hrp-encoded type III protein secretion in Pseudomonas syringae strains | Q33996908 | ||
| Genomewide identification of Pseudomonas syringae pv. tomato DC3000 promoters controlled by the HrpL alternative sigma factor | Q34013057 | ||
| Direct biochemical evidence for type III secretion-dependent translocation of the AvrBs2 effector protein into plant cells | Q34032589 | ||
| Assembly and function of type III secretory systems | Q34052773 | ||
| In vivo rho GTPase-activating protein activity of Pseudomonas aeruginosa cytotoxin ExoS | Q34116489 | ||
| Common and contrasting themes of plant and animal diseases | Q34292177 | ||
| Yersinia type III secretion: send in the effectors | Q34774578 | ||
| A conserved amino acid sequence directing intracellular type III secretion by Salmonella typhimurium | Q35162771 | ||
| The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death | Q35630003 | ||
| Identification of a pathogenicity island, which contains genes for virulence and avirulence, on a large native plasmid in the bean pathogen Pseudomonas syringae pathovar phaseolicola | Q35635473 | ||
| 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 | Q35699642 | ||
| Hrp pilus: an hrp-dependent bacterial surface appendage produced by Pseudomonas syringae pv. tomato DC3000 | Q36086934 | ||
| Molecular analysis of avirulence gene avrRpt2 and identification of a putative regulatory sequence common to all known Pseudomonas syringae avirulence genes | Q36103789 | ||
| Characterization of the promoter of avirulence gene D from Pseudomonas syringae pv. tomato | Q36122224 | ||
| A cloned Erwinia chrysanthemi Hrp (type III protein secretion) system functions in Escherichia coli to deliver Pseudomonas syringae Avr signals to plant cells and to secrete Avr proteins in culture | Q36289429 | ||
| Reciprocal secretion of proteins by the bacterial type III machines of plant and animal pathogens suggests universal recognition of mRNA targeting signals | Q36559367 | ||
| Molecular signals required for type III secretion and translocation of the Xanthomonas campestris AvrBs2 protein to pepper plants | Q37293186 | ||
| The alternative sigma factor RpoN is required for hrp activity in Pseudomonas syringae pv. maculicola and acts at the level of hrpL transcription | Q39539015 | ||
| The Hrp pilus of Pseudomonas syringae elongates from its tip and acts as a conduit for translocation of the effector protein HrpZ. | Q39644861 | ||
| P433 | issue | 10 | |
| P921 | main subject | Pseudomonas syringae | Q311202 |
| P304 | page(s) | 462-469 | |
| P577 | publication date | 2002-10-01 | |
| P1433 | published in | Trends in Microbiology | Q15265732 |
| P1476 | title | Genomic mining type III secretion system effectors in Pseudomonas syringae yields new picks for all TTSS prospectors | |
| P478 | volume | 10 |
| Q64093308 | A Novel Effector Gene SCRE2 Contributes to Full Virulence of Ustilaginoidea virens to Rice |
| Q35168706 | A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants |
| Q50089577 | A chaperone-like HrpG protein acts as a suppressor of HrpV in regulation of the Pseudomonas syringae pv. syringae type III secretion system. |
| Q37864748 | A directed screen for chlamydial proteins secreted by a type III mechanism identifies a translocated protein and numerous other new candidates |
| Q33496332 | A draft genome sequence and functional screen reveals the repertoire of type III secreted proteins of Pseudomonas syringae pathovar tabaci 11528 |
| Q36449475 | A family of conserved bacterial effectors inhibits salicylic acid-mediated basal immunity and promotes disease necrosis in plants |
| Q33850561 | A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae |
| Q34589927 | A highly-conserved single-stranded DNA-binding protein in Xanthomonas functions as a harpin-like protein to trigger plant immunity |
| Q33196497 | A novel secreted protein toxin from the insect pathogenic bacterium Xenorhabdus nematophila |
| Q35982125 | A widespread bacterial type VI secretion effector superfamily identified using a heuristic approach |
| Q33434470 | Accurate prediction of secreted substrates and identification of a conserved putative secretion signal for type III secretion systems |
| Q44751581 | Activation of a COI1-dependent pathway in Arabidopsis by Pseudomonas syringae type III effectors and coronatine |
| Q45945199 | An account of in silico identification tools of secreted effector proteins in bacteria and future challenges. |
| Q33836262 | An ancestral oomycete locus contains late blight avirulence gene Avr3a, encoding a protein that is recognized in the host cytoplasm |
| Q24678382 | An extensive repertoire of type III secretion effectors in Escherichia coli O157 and the role of lambdoid phages in their dissemination |
| Q41450750 | Analyses of the secretomes of Erwinia amylovora and selected hrp mutants reveal novel type III secreted proteins and an effect of HrpJ on extracellular harpin levels. |
| Q52549320 | Arabidopsis RIN4 is a target of the type III virulence effector AvrRpt2 and modulates RPS2-mediated resistance. |
| Q53885741 | Arabidopsis RIN4 negatively regulates disease resistance mediated by RPS2 and RPM1 downstream or independent of the NDR1 signal modulator and is not required for the virulence functions of bacterial type III effectors AvrRpt2 or AvrRpm1. |
| Q36088671 | Bioinformatics, genomics and evolution of non-flagellar type-III secretion systems: a Darwinian perspective |
| Q40867634 | Characterization of the cis-acting regulatory element controlling HrpB-mediated activation of the type III secretion system and effector genes in Ralstonia solanacearum. |
| Q30320629 | Common infection strategies of plant and animal pathogenic bacteria |
| Q51671058 | Comparative analysis of metabolic networks provides insight into the evolution of plant pathogenic and nonpathogenic lifestyles in Pseudomonas. |
| Q33714608 | Comparative genomic analysis of the pPT23A plasmid family of Pseudomonas syringae |
| Q33503402 | Comparative in vivo gene expression of the closely related bacteria Photorhabdus temperata and Xenorhabdus koppenhoeferi upon infection of the same insect host, Rhizotrogus majalis |
| Q31028145 | Complete nucleotide sequence and analysis of pPSR1 (72,601 bp), a pPT23A-family plasmid from Pseudomonas syringae pv. syringae A2. |
| Q54987424 | Differential Suppression of Nicotiana benthamiana Innate Immune Responses by Transiently Expressed Pseudomonas syringae Type III Effectors. |
| Q35911179 | Disabling surveillance: bacterial type III secretion system effectors that suppress innate immunity |
| Q37074383 | Dissecting virulence: systematic and functional analyses of a pathogenicity island |
| Q34645388 | Diverse evolutionary mechanisms shape the type III effector virulence factor repertoire in the plant pathogen Pseudomonas syringae |
| Q37542383 | Establishment of an inducing medium for type III effector secretion in Xanthomonas campestris pv. campestris |
| Q46595106 | Eukaryotic cyclophilin as a molecular switch for effector activation. |
| Q43723272 | Gene-for-gene relationship in the host-pathogen system Malus × robusta 5-Erwinia amylovora |
| Q33728171 | Genome-wide identification of HrpL-regulated genes in the necrotrophic phytopathogen Dickeya dadantii 3937. |
| Q35234956 | Global analysis of the HrpL regulon in the plant pathogen Pseudomonas syringae pv. tomato DC3000 reveals new regulon members with diverse functions |
| Q37374881 | Horizontal gene transfer: sustaining pathogenicity and optimizing host-pathogen interactions |
| Q46884639 | Host-mediated phosphorylation of type III effector AvrPto promotes Pseudomonas virulence and avirulence in tomato. |
| Q48207372 | Identification of Pseudomonas syringae type III effectors that can suppress programmed cell death in plants and yeast |
| Q34231086 | Identification of a twin-arginine translocation system in Pseudomonas syringae pv. tomato DC3000 and its contribution to pathogenicity and fitness |
| Q35604905 | Inhibitor of apoptosis (IAP)-like protein lacks a baculovirus IAP repeat (BIR) domain and attenuates cell death in plant and animal systems |
| Q42466386 | Interaction-dependent gene expression in Mla-specified response to barley powdery mildew |
| Q35159314 | Interleukin-10 and inhibition of innate immunity to Yersiniae: roles of Yops and LcrV (V antigen) |
| Q21194850 | MYRbase: analysis of genome-wide glycine myristoylation enlarges the functional spectrum of eukaryotic myristoylated proteins |
| Q45880921 | Mi Casa es Su Casa: how an intracellular symbiont manipulates host biology |
| Q40524232 | Microbiota is a primary cause of pathogenesis of chronic wounds |
| Q34562599 | Mutation in the xpsD gene of Xanthomonas axonopodis pv. citri affects cellulose degradation and virulence |
| Q34589093 | Natural variation in the Pto pathogen resistance gene within species of wild tomato (Lycopersicon). I. Functional analysis of Pto alleles |
| Q37461173 | Negative regulation of pathogenesis in Pseudomonas syringae pv. tabaci 11528 by ATP-dependent Lon protease |
| Q44655598 | New effects of type III effectors |
| Q37766936 | Pathogenicity and other genomic islands in plant pathogenic bacteria |
| Q35127920 | Plant pathology: monitoring a pathogen-targeted host protein |
| Q33928688 | Powerful screens for bacterial virulence 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 |
| 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 |
| Q33345234 | Quorum sensing coordinates brute force and stealth modes of infection in the plant pathogen Pectobacterium atrosepticum |
| Q36534493 | RXLR effector reservoir in two Phytophthora species is dominated by a single rapidly evolving superfamily with more than 700 members |
| Q42727344 | Regulation of type III secretion hierarchy of translocators and effectors in attaching and effacing bacterial pathogens |
| 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. |
| Q45949103 | Revealing the inventory of type III effectors in Pantoea agglomerans gall-forming pathovars by using draft genome sequences and a machine-learning approach. |
| Q37473945 | Roadmap for future research on plant pathogen effectors |
| Q28775800 | Role of type III effector secretion during bacterial pathogenesis in another kingdom |
| Q39691140 | Selective Photoreceptor Gene Knock-out Reveals a Regulatory Role for the Growth Behavior of Pseudomonas syringae |
| Q33883322 | SepZ/EspZ is secreted and translocated into HeLa cells by the enteropathogenic Escherichia coli type III secretion system |
| Q35025547 | Technologies and approaches to elucidate and model the virulence program of salmonella |
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| 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 |
| Q43786768 | The Pseudomonas syringae effector HopQ1 promotes bacterial virulence and interacts with tomato 14-3-3 proteins in a phosphorylation-dependent manner |
| Q43010978 | The Pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid-dependent defences in Arabidopsis thaliana |
| Q64273419 | The Role of Proteases in the Virulence of Plant Pathogenic Bacteria |
| Q22066254 | The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000 |
| Q35980437 | The cytoskeleton as a regulator and target of biotic interactions in plants |
| Q48075696 | The downy mildew effector proteins ATR1 and ATR13 promote disease susceptibility in Arabidopsis thaliana |
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