review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0966-842X(00)01751-0 |
P698 | PubMed publication ID | 10785634 |
P2093 | author name string | J C Bennett | |
C Hughes | |||
P2860 | cites work | Following the leader: bacterial protein export through the Sec pathway. | Q33702236 |
Identification of a specific chaperone for SptP, a substrate of the centisome 63 type III secretion system of Salmonella typhimurium. | Q33732554 | ||
Supramolecular structure of the Salmonella typhimurium type III protein secretion system | Q34746894 | ||
Homologs of the Shigella IpaB and IpaC invasins are required for Salmonella typhimurium entry into cultured epithelial cells | Q35589961 | ||
Individual chaperones required for Yop secretion by Yersinia | Q35858391 | ||
SycE, a chaperone-like protein of Yersinia enterocolitica involved in Ohe secretion of YopE. | Q36783256 | ||
Identification of CesT, a chaperone for the type III secretion of Tir in enteropathogenic Escherichia coli. | Q38319836 | ||
Enteropathogenic Escherichia coli translocated intimin receptor, Tir, requires a specific chaperone for stable secretion | Q38319840 | ||
A complex composed of SycN and YscB functions as a specific chaperone for YopN in Yersinia pestis | Q41483344 | ||
Role of SycD, the chaperone of the Yersinia Yop translocators YopB and YopD. | Q41483801 | ||
YopT, a new Yersinia Yop effector protein, affects the cytoskeleton of host cells. | Q41485138 | ||
A mRNA signal for the type III secretion of Yop proteins by Yersinia enterocolitica | Q41487461 | ||
Two independent type III secretion mechanisms for YopE in Yersinia enterocolitica | Q41488408 | ||
The cytosolic SycE and SycH chaperones of Yersinia protect the region of YopE and YopH involved in translocation across eukaryotic cell membranes | Q41491050 | ||
Extracellular association and cytoplasmic partitioning of the IpaB and IpaC invasins of S. flexneri | Q41497452 | ||
A motile but non-swarming mutant of Proteus mirabilis lacks FlgN, a facilitator of flagella filament assembly | Q48046311 | ||
Substrate-specific binding of hook-associated proteins by FlgN and FliT, putative chaperones for flagellum assembly | Q48565780 | ||
Functional analysis of the flagellar genes in the fliD operon of Salmonella typhimurium | Q50143216 | ||
EspB and EspD require a specific chaperone for proper secretion from enteropathogenicEscherichia coli | Q59307488 | ||
P433 | issue | 5 | |
P921 | main subject | molecular chaperones | Q422496 |
P304 | page(s) | 202-204 | |
P577 | publication date | 2000-05-01 | |
P1433 | published in | Trends in Microbiology | Q15265732 |
P1476 | title | From flagellum assembly to virulence: the extended family of type III export chaperones | |
P478 | volume | 8 |
Q41435019 | A dominant-negative needle mutant blocks type III secretion of early but not late substrates in Yersinia |
Q37692988 | A genetic screen to isolate type III effectors translocated into pepper cells during Xanthomonas infection |
Q41195489 | A specific genomic location within the icm/dot pathogenesis region of different Legionella species encodes functionally similar but nonhomologous virulence proteins |
Q46008443 | Architecture of the type IV coupling protein complex of Legionella pneumophila. |
Q41411817 | Assembly of the Yersinia injectisome: the missing pieces. |
Q34067874 | Bacterial interplay at intestinal mucosal surfaces: implications for vaccine development |
Q39741755 | CesD2 of enteropathogenic Escherichia coli is a second chaperone for the type III secretion translocator protein EspD. |
Q54479840 | CesT is a multi-effector chaperone and recruitment factor required for the efficient type III secretion of both LEE- and non-LEE-encoded effectors of enteropathogenic Escherichia coli. |
Q34941907 | Chaperones of the type III secretion pathway: jacks of all trades |
Q54275279 | Characterization of Helicobacter pylori HP0231 (DsbK): role in disulfide bond formation, redox homeostasis and production of Helicobacter cystein-rich protein HcpE. |
Q34786208 | Coiled-coil proteins associated with type III secretion systems: a versatile domain revisited |
Q45340373 | Computationally identifying virulence factors based on KEGG pathways |
Q34010272 | Coupling of flagellar gene expression to flagellar assembly in Salmonella enterica serovar typhimurium and Escherichia coli |
Q30475802 | Crystal structure of the flagellar rotor protein FliN from Thermotoga maritima |
Q80803577 | Diversity of fliC gene in commensal Escherichia coli derived from various mammals |
Q37095412 | Docking of cytosolic chaperone-substrate complexes at the membrane ATPase during flagellar type III protein export |
Q37263766 | Energizing type III secretion machines: what is the fuel? |
Q42425518 | Flagellin polymerisation control by a cytosolic export chaperone. |
Q33743275 | FlgN is required for flagellum-based motility by Bacillus subtilis |
Q41394221 | FliS modulates FlgM activity by acting as a non-canonical chaperone to control late flagellar gene expression, motility and biofilm formation in Yersinia pseudotuberculosis |
Q50111069 | Functional analysis of the enteropathogenic Escherichia coli type III secretion system chaperone CesT identifies domains that mediate substrate interactions |
Q37410187 | Functional characterization of SsaE, a novel chaperone protein of the type III secretion system encoded by Salmonella pathogenicity island 2. |
Q42675434 | Functional characterization of the antagonistic flagellar late regulators FliA and FlgM of Helicobacter pylori and their effects on the H. pylori transcriptome |
Q30320765 | Getting across--bacterial type III effector proteins on their way to the plant cell |
Q34194719 | How Bacteria Assemble Flagella |
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 |
Q34513676 | Identification of new flagellar genes of Salmonella enterica serovar Typhimurium |
Q34595020 | Identification of novel type III secretion chaperone-substrate complexes of Chlamydia trachomatis |
Q42228105 | Identification of the DotL coupling protein subcomplex of the Legionella Dot/Icm type IV secretion system |
Q43463077 | Inactivation of Helicobacter pylori cagA gene affects motility. |
Q39887119 | Interactions of FliJ with the Salmonella type III flagellar export apparatus |
Q42425520 | Intrinsic membrane targeting of the flagellar export ATPase FliI: interaction with acidic phospholipids and FliH. |
Q33792217 | InvB is a type III secretion chaperone specific for SspA. |
Q35942335 | Involvement of the flagellar assembly pathway in Vibrio alginolyticus adhesion under environmental stresses |
Q40454544 | IpaD of Shigella flexneri is independently required for regulation of Ipa protein secretion and efficient insertion of IpaB and IpaC into host membranes. |
Q40949451 | Maf-dependent bacterial flagellin glycosylation occurs before chaperone binding and flagellar T3SS export |
Q27635933 | Maintenance of an unfolded polypeptide by a cognate chaperone in bacterial type III secretion |
Q50108067 | Molecular dissection of Salmonella FliH, a regulator of the ATPase FliI and the type III flagellar protein export pathway. |
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. |
Q41439802 | Selective binding of virulence type III export chaperones by FliJ escort orthologues InvI and YscO. |
Q27641967 | Similar modes of polypeptide recognition by export chaperones in flagellar biosynthesis and type III secretion |
Q27643589 | Structural analysis of a prototypical ATPase from the type III secretion system |
Q39730227 | Structural characterization of the N terminus of IpaC from Shigella flexneri |
Q49967370 | Structural plasticity of the Salmonella FliS flagellar export chaperone |
Q42136963 | Substrate complexes and domain organization of the Salmonella flagellar export chaperones FlgN and FliT. |
Q35371304 | Tandem translation generates a chaperone for the Salmonella type III secretion system protein SsaQ |
Q41455790 | Tetratricopeptide repeats in the type III secretion chaperone, LcrH: their role in substrate binding and secretion |
Q33551064 | The HP0256 gene product is involved in motility and cell envelope architecture of Helicobacter pylori |
Q47208585 | The Legionella pneumophila IcmR protein exhibits chaperone activity for IcmQ by preventing its participation in high-molecular-weight complexes |
Q40262478 | The Legionella pneumophila IcmS-LvgA protein complex is important for Dot/Icm-dependent intracellular growth |
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 |
Q53871902 | The ShcA protein is a molecular chaperone that assists in the secretion of the HopPsyA effector from the type III (Hrp) protein secretion system of Pseudomonas syringae. |
Q35050399 | The Type III secretion system of Gram-negative bacteria: a potential therapeutic target? |
Q28252092 | The bacterial flagellar motor: structure and function of a complex molecular machine |
Q41953200 | The flagellar-specific transcription factor, sigma28, is the Type III secretion chaperone for the flagellar-specific anti-sigma28 factor FlgM |
Q35079368 | The multitalented type III chaperones: all you can do with 15 kDa. |
Q41473734 | The type III secretion chaperone LcrH co-operates with YopD to establish a negative, regulatory loop for control of Yop synthesis in Yersinia pseudotuberculosis |
Q29617944 | The type III secretion injectisome |
Q34697291 | Transcriptional and translational control of the Salmonella fliC gene |
Q59210021 | Translation/Secretion Coupling by Type III Secretion Systems |
Q40173948 | Translocated Intimin Receptor and Its Chaperone Interact with ATPase of the Type III Secretion Apparatus of EnteropathogenicEscherichia coli |
Q34222731 | Type III export: new uses for an old pathway |
Q36224498 | Type III secretion: a secretory pathway serving both motility and virulence (review). |
Q39516968 | Yersinia pestis YscG protein is a Syc-like chaperone that directly binds yscE. |
Q39529389 | toxB gene on pO157 of enterohemorrhagic Escherichia coli O157:H7 is required for full epithelial cell adherence phenotype |
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