scholarly article | Q13442814 |
P2093 | author name string | John Mansfield | |
Ian Brown | |||
Martin Romantschuk | |||
Chun-Mei Li | |||
Suvi Taira | |||
Tristan Boureau | |||
Conrad Stevens | |||
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Maintenance of an unfolded polypeptide by a cognate chaperone in bacterial type III secretion | Q27635933 | ||
Two simple media for the demonstration of pyocyanin and fluorescin | Q28210604 | ||
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 | ||
Mutational analysis of the Pseudomonas syringae pv. tomato hrpA gene encoding Hrp pilus subunit | Q30813647 | ||
Type III secretion machines: bacterial devices for protein delivery into host cells | Q33639326 | ||
The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes | Q33878820 | ||
A novel EspA-associated surface organelle of enteropathogenic Escherichia coli involved in protein translocation into epithelial cells | Q33888663 | ||
HrpZPsph from the plant pathogen Pseudomonas syringae pv. phaseolicola binds to lipid bilayers and forms an ion-conducting pore in vitro | Q33929605 | ||
Supermolecular structure of the enteropathogenic Escherichia coli type III secretion system and its direct interaction with the EspA-sheath-like structure | Q33944789 | ||
Bacterial blight of soybean: regulation of a pathogen gene determining host cultivar specificity | Q34544077 | ||
Supramolecular structure of the Salmonella typhimurium type III protein secretion system | Q34746894 | ||
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 | Q35052377 | ||
Polymerization of a single protein of the pathogen Yersinia enterocolitica into needles punctures eukaryotic cells | Q35290671 | ||
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 | ||
Hrp pilus: an hrp-dependent bacterial surface appendage produced by Pseudomonas syringae pv. tomato DC3000 | Q36086934 | ||
Biogenesis of the bacterial pilus | Q36553245 | ||
Mercuric ion-resistance operons of plasmid R100 and transposon Tn501: the beginning of the operon including the regulatory region and the first two structural genes | Q37569888 | ||
Cultivar-specific avirulence and virulence functions assigned to avrPphF in Pseudomonas syringae pv. phaseolicola, the cause of bean halo-blight disease. | Q40430057 | ||
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 | ||
EspA filament-mediated protein translocation into red blood cells | Q40813279 | ||
Contact with epithelial cells induces the formation of surface appendages on Salmonella typhimurium | Q41486433 | ||
Immunocytochemical localization of HrpA and HrpZ supports a role for the Hrp pilus in the transfer of effector proteins from Pseudomonas syringae pv. tomato across the host plant cell wall | Q42501911 | ||
Sequence variations in alleles of the avirulence gene avrPphE.R2 from Pseudomonas syringae pv. phaseolicola lead to loss of recognition of the AvrPphE protein within bean cells and a gain in cultivar-specific virulence | Q47694494 | ||
pBBR1MCS: a broad-host-range cloning vector | Q48082899 | ||
Structure of the core and central channel of bacterial flagella. | Q50192817 | ||
The Coiled-coil Domain of EspA Is Essential for the Assembly of the Type III Secretion Translocon on the Surface of EnteropathogenicEscherichia coli | Q57819086 | ||
Visualization of secreted Hrp and Avr proteins along the Hrp pilus during type III secretion in Erwinia amylovora and Pseudomonas syringae | Q64449576 | ||
Immunogold labeling of Hrp pili of Pseudomonas syringae pv. tomato assembled in minimal medium and in planta | Q64449613 | ||
Ralstonia solanacearum produces hrp-dependent pili that are required for PopA secretion but not for attachment of bacteria to plant cells | Q64449692 | ||
Purified HrpA of Pseudomonas syringae pv. tomato DC3000 reassembles into pili | Q73934669 | ||
Construction and Use of Broad Host Range Mercury and Arsenite Sensor Plasmids in the Soil Bacterium Pseudomonas fluorescens OS8 | Q74183272 | ||
Initial binding of Shiga toxin-producing Escherichia coli to host cells and subsequent induction of actin rearrangements depend on filamentous EspA-containing surface appendages | Q77456473 | ||
Bacterial avirulence genes | Q79760388 | ||
Bacterial Flagella: Polarity of Elongation | Q93803896 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Pseudomonas syringae | Q311202 |
P304 | page(s) | 1909-1915 | |
P577 | publication date | 2002-04-01 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | The Hrp pilus of Pseudomonas syringae elongates from its tip and acts as a conduit for translocation of the effector protein HrpZ. | |
P478 | volume | 21 |
Q90345387 | A Computation Method Based on the Combination of Chlorophyll Fluorescence Parameters to Improve the Discrimination of Visually Similar Phenotypes Induced by Bacterial Virulence Factors |
Q41435019 | A dominant-negative needle mutant blocks type III secretion of early but not late substrates in Yersinia |
Q33345500 | A genome-wide functional investigation into the roles of receptor-like proteins in Arabidopsis |
Q37230906 | Architectures and biogenesis of non-flagellar protein appendages in Gram-negative bacteria |
Q39230405 | Assembly, structure, function and regulation of type III secretion systems. |
Q35132216 | Bacterial injection machines |
Q28068755 | Behind the lines-actions of bacterial type III effector proteins in plant cells |
Q79204518 | Characterization of the hrp pathogenicity cluster of Erwinia carotovora subsp. carotovora: high basal level expression in a mutant is associated with reduced virulence |
Q30320629 | Common infection strategies of plant and animal pathogenic bacteria |
Q34194984 | Deciphering plant–pathogen communication: fresh perspectives for molecular resistance breeding |
Q33937826 | Domain structure of HrpE, the Hrp pilus subunit of Xanthomonas campestris pv. vesicatoria |
Q35198119 | Establishing order for type III secretion substrates--a hierarchical process |
Q40444525 | Evaluation of a loop-mediated isothermal amplification assay based on hrpZ gene for rapid detection and identification of Pseudomonas syringae pv. lachrymans in cucumber leaves |
Q36740760 | Folding kinetics and thermodynamics of Pseudomonas syringae effector protein AvrPto provide insight into translocation via the type III secretion system |
Q28262210 | From bacterial avirulence genes to effector functions via the hrp delivery system: an overview of 25 years of progress in our understanding of plant innate immunity |
Q34157255 | Functional mapping of harpin HrpZ of Pseudomonas syringae reveals the sites responsible for protein oligomerization, lipid interactions and plant defence induction |
Q34960211 | Genomic mining type III secretion system effectors in Pseudomonas syringae yields new picks for all TTSS prospectors |
Q30320765 | Getting across--bacterial type III effector proteins on their way to the plant cell |
Q34068346 | Length control of the injectisome needle requires only one molecule of Yop secretion protein P (YscP). |
Q47794449 | Localization of hrpA-induced Pseudomonas syringae pv. tomato DC3000 in infected tomato leaves |
Q50998985 | Lon protease modulates virulence traits in Erwinia amylovora by direct monitoring of major regulators and indirectly through the Rcs and Gac-Csr regulatory systems. |
Q41414165 | Multiple lessons from the multiple functions of a regulator of type III secretion system assembly in the plant pathogen Pseudomonas syringae |
Q37766936 | Pathogenicity and other genomic islands in plant pathogenic bacteria |
Q40439695 | Polarity of enteropathogenic Escherichia coli EspA filament assembly and protein secretion |
Q34697819 | PopF1 and PopF2, two proteins secreted by the type III protein secretion system of Ralstonia solanacearum, are translocators belonging to the HrpF/NopX family |
Q35980175 | Process of protein transport by the type III secretion system |
Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
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 |
Q37897277 | Pseudomonas syringae pv. phaseolicola: from 'has bean' to supermodel. |
Q28775800 | Role of type III effector secretion during bacterial pathogenesis in another kingdom |
Q30318497 | Secretion of early and late substrates of the type III secretion system from Xanthomonas is controlled by HpaC and the C-terminal domain of HrcU. |
Q36427172 | Supramolecular Structure and Functional Analysis of the Type III Secretion System in Pseudomonas fluorescens 2P24. |
Q42482994 | The PscE-PscF-PscG complex controls type III secretion needle biogenesis in Pseudomonas aeruginosa |
Q54502252 | The bacterial type III secretion system-associated pilin HrpA has an unusually long mRNA half-life. |
Q35079368 | The multitalented type III chaperones: all you can do with 15 kDa. |
Q40241309 | The pathogenicity factor HrpF interacts with HrpA and HrpG to modulate type III secretion system (T3SS) function and t3ss expression in Pseudomonas syringae pv. averrhoi. |
Q29617944 | The type III secretion injectisome |
Q37756149 | The type III secretion injectisome, a complex nanomachine for intracellular 'toxin' delivery |
Q30320262 | The type III-dependent Hrp pilus is required for productive interaction of Xanthomonas campestris pv. vesicatoria with pepper host plants |
Q37665331 | Timing is everything: the regulation of type III secretion |
Q34032225 | Top 10 plant pathogenic bacteria in molecular plant pathology |
Q35111427 | Type III protein secretion in Pseudomonas syringae |
Q37490586 | Type III protein secretion in plant pathogenic bacteria |
Q42440794 | Type III protein translocase: HrcN is a peripheral ATPase that is activated by oligomerization |
Q36224498 | Type III secretion: a secretory pathway serving both motility and virulence (review). |
Q92956497 | Unusual extracellular appendages deployed by the model strain Pseudomonas fluorescens C7R12 |
Q54488870 | Use of dominant-negative HrpA mutants to dissect Hrp pilus assembly and type III secretion in Pseudomonas syringae pv. tomato. |
Q30479614 | YscU recognizes translocators as export substrates of the Yersinia injectisome |
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