scholarly article | Q13442814 |
P2093 | author name string | Isabel Martinez-Argudo | |
Ariel J Blocker | |||
P2860 | cites work | TyeA, a protein involved in control of Yop release and in translocation of Yersinia Yop effectors. | Q24533192 |
LcrG-LcrV interaction is required for control of Yops secretion in Yersinia pestis | Q24548891 | ||
Bioinformatics analysis of the locus for enterocyte effacement provides novel insights into type-III secretion | Q24791468 | ||
Structures of the Shigella flexneri Type 3 Secretion System Protein MxiC Reveal Conformational Variability Amongst Homologues | Q27649946 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Structure and composition of the Shigella flexneri "needle complex", a part of its type III secreton | Q28199735 | ||
Protein delivery into eukaryotic cells by type III secretion machines | Q28276443 | ||
pH Sensing by Intracellular Salmonella Induces Effector Translocation | Q29037234 | ||
The type III secretion injectisome | Q29617944 | ||
ExoS controls the cell contact-mediated switch to effector secretion in Pseudomonas aeruginosa | Q30481673 | ||
The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes | Q33878820 | ||
Characterization of SepL of enterohemorrhagic Escherichia coli | Q33994963 | ||
Spa32 regulates a switch in substrate specificity of the type III secreton of Shigella flexneri from needle components to Ipa proteins | Q34314419 | ||
Salmonella type III secretion-associated protein InvE controls translocation of effector proteins into host cells | Q34317570 | ||
Identification of new flagellar genes of Salmonella enterica serovar Typhimurium | Q34513676 | ||
Supramolecular structure of the Salmonella typhimurium type III protein secretion system | Q34746894 | ||
Control of effector export by the Pseudomonas aeruginosa type III secretion proteins PcrG and PcrV. | Q35071514 | ||
Yersinia pestis LcrV forms a stable complex with LcrG and may have a secretion-related regulatory role in the low-Ca2+ response | Q35620091 | ||
Self-chaperoning of the type III secretion system needle tip proteins IpaD and BipD. | Q35846739 | ||
Nonpolar mutagenesis of the ipa genes defines IpaB, IpaC, and IpaD as effectors of Shigella flexneri entry into epithelial cells | Q36122200 | ||
Molecular pathogenesis of Shigella spp.: controlling host cell signaling, invasion, and death by type III secretion. | Q36422508 | ||
Involvement of a plasmid in the invasive ability of Shigella flexneri. | Q36437346 | ||
What's the point of the type III secretion system needle? | Q36638746 | ||
Dissecting virulence: systematic and functional analyses of a pathogenicity island | Q37074383 | ||
Timing is everything: the regulation of type III secretion | Q37665331 | ||
Secretion of Ipa proteins by Shigella flexneri: inducer molecules and kinetics of activation. | Q39831093 | ||
The extreme C terminus of Shigella flexneri IpaB is required for regulation of type III secretion, needle tip composition, and binding. | Q39896038 | ||
Mutations in the Yersinia pseudotuberculosis type III secretion system needle protein, YscF, that specifically abrogate effector translocation into host cells | Q40214494 | ||
IpaD of Shigella flexneri is independently required for regulation of Ipa protein secretion and efficient insertion of IpaB and IpaC into host membranes. | Q40454544 | ||
Shigella flexneri: genetics of entry and intercellular dissemination in epithelial cells | Q40595493 | ||
The secretion of the Shigella flexneri Ipa invasins is activated by epithelial cells and controlled by IpaB and IpaD. | Q40793797 | ||
Gene expression profiling of Yersinia pestis with deletion of lcrG, a known negative regulator for Yop secretion of type III secretion system | Q41440817 | ||
The Yersinia pestis type III secretion needle plays a role in the regulation of Yop secretion | Q41457055 | ||
Selection and characterization of Yersinia pestis YopN mutants that constitutively block Yop secretion. | Q41457355 | ||
MxiK and MxiN interact with the Spa47 ATPase and are required for transit of the needle components MxiH and MxiI, but not of Ipa proteins, through the type III secretion apparatus of Shigella flexneri | Q41466218 | ||
Translocation of YopE and YopN into eukaryotic cells by Yersinia pestis yopN, tyeA, sycN, yscB and lcrG deletion mutants measured using a phosphorylatable peptide tag and phosphospecific antibodies | Q41469138 | ||
MxiG, a membrane protein required for secretion of Shigella spp. Ipa invasins: involvement in entry into epithelial cells and in intercellular dissemination | Q41493869 | ||
The surface-located YopN protein is involved in calcium signal transduction inYersinia pseudotuberculosis | Q41509042 | ||
IpaD localizes to the tip of the type III secretion system needle of Shigella flexneri | Q41856079 | ||
Liposomes recruit IpaC to the Shigella flexneri type III secretion apparatus needle as a final step in secretion induction. | Q42128361 | ||
Shigella Spa33 is an essential C-ring component of type III secretion machinery | Q42485719 | ||
Regulation of type III secretion hierarchy of translocators and effectors in attaching and effacing bacterial pathogens | Q42727344 | ||
Bile salts stimulate recruitment of IpaB to the Shigella flexneri surface, where it colocalizes with IpaD at the tip of the type III secretion needle | Q42799643 | ||
Hierarchal type III secretion of translocators and effectors from Escherichia coli O157:H7 requires the carboxy terminus of SepL that binds to Tir. | Q46450220 | ||
SepL, a protein required for enteropathogenic Escherichia coli type III translocation, interacts with secretion component SepD. | Q47373545 | ||
A set of compatible tac promoter expression vectors | Q48058798 | ||
Expression and secretion of Salmonella pathogenicity island-2 virulence genes in response to acidification exhibit differential requirements of a functional type III secretion apparatus and SsaL. | Q50096705 | ||
Identification of minor inner-membrane components of the Shigella type III secretion system 'needle complex'. | Q53566059 | ||
The type III secretion system needle tip complex mediates host cell sensing and translocon insertion. | Q53575352 | ||
Regulation of transcription by the activity of the Shigella flexneri type III secretion apparatus. | Q54546861 | ||
Helical Packing of Needles from Functionally Altered Shigella Type III Secretion Systems | Q57836628 | ||
Characterization of soluble complexes of theShigella flexneritype III secretion system ATPase | Q57843640 | ||
Enhanced secretion through the Shigella flexneri Mxi-Spa translocon leads to assembly of extracellular proteins into macromolecular structures | Q64360979 | ||
The needle component of the type III secreton of Shigella regulates the activity of the secretion apparatus | Q81355843 | ||
Analysis of virulence plasmid gene expression defines three classes of effectors in the type III secretion system of Shigella flexneri | Q81503204 | ||
A secreted anti-activator, OspD1, and its chaperone, Spa15, are involved in the control of transcription by the type III secretion apparatus activity in Shigella flexneri | Q81785474 | ||
MxiC is secreted by and controls the substrate specificity of the Shigella flexneri type III secretion apparatus | Q82645592 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1365-1378 | |
P577 | publication date | 2010-10-12 | |
P1433 | published in | Molecular Microbiology | Q6895967 |
P1476 | title | The Shigella T3SS needle transmits a signal for MxiC release, which controls secretion of effectors | |
P478 | volume | 78 |
Q41006822 | A dynamic and adaptive network of cytosolic interactions governs protein export by the T3SS injectisome |
Q35398859 | A gatekeeper chaperone complex directs translocator secretion during type three secretion |
Q38127453 | A sophisticated multi-step secretion mechanism: how the type 3 secretion system is regulated |
Q38183945 | Assembly of the bacterial type III secretion machinery. |
Q39230405 | Assembly, structure, function and regulation of type III secretion systems. |
Q30389751 | Chlamydia pneumoniae effector chlamydial outer protein N sequesters fructose bisphosphate aldolase A, providing a benefit to bacterial growth |
Q33627041 | Control of type III secretion activity and substrate specificity by the cytoplasmic regulator PcrG. |
Q39192014 | Functional insights into the Shigella type III needle tip IpaD in secretion control and cell contact. |
Q42736388 | Genetic Dissection of the Signaling Cascade that Controls Activation of the Shigella Type III Secretion System from the Needle Tip. |
Q35009783 | Genetically engineered frameshifted YopN-TyeA chimeras influence type III secretion system function in Yersinia pseudotuberculosis |
Q39230762 | How Do the Virulence Factors of Shigella Work Together to Cause Disease? |
Q60049375 | Identification of specific sequence motif of YopN of Yersinia pseudotuberculosis required for systemic infection |
Q39464419 | Impact of the N-terminal secretor domain on YopD translocator function in Yersinia pseudotuberculosis type III secretion |
Q26750857 | Implications of Spatiotemporal Regulation of Shigella flexneri Type Three Secretion Activity on Effector Functions: Think Globally, Act Locally |
Q41402188 | Interplay between predicted inner-rod and gatekeeper in controlling substrate specificity of the type III secretion system |
Q28484814 | Isolation of Salmonella mutants resistant to the inhibitory effect of Salicylidene acylhydrazides on flagella-mediated motility |
Q28492629 | Modified needle-tip PcrV proteins reveal distinct phenotypes relevant to the control of type III secretion and intoxication by Pseudomonas aeruginosa |
Q30431366 | Multi-Functional Characteristics of the Pseudomonas aeruginosa Type III Needle-Tip Protein, PcrV; Comparison to Orthologs in other Gram-negative Bacteria |
Q41414165 | Multiple lessons from the multiple functions of a regulator of type III secretion system assembly in the plant pathogen Pseudomonas syringae |
Q90091019 | Multiple proteins arising from a single gene: The role of the Spa33 variants in Shigella T3SS regulation |
Q36015449 | MxiA, MxiC and IpaD Regulate Substrate Selection and Secretion Mode in the T3SS of Shigella flexneri |
Q82706286 | MxiC: the gatekeeper |
Q41823389 | Needle length control and the secretion substrate specificity switch are only loosely coupled in the type III secretion apparatus of Shigella |
Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
Q40463683 | Reassessment of MxiH subunit orientation and fold within native Shigella T3SS needles using surface labelling and solid-state NMR. |
Q35096446 | Scc1 (CP0432) and Scc4 (CP0033) function as a type III secretion chaperone for CopN of Chlamydia pneumoniae |
Q42128393 | Shigella IpaD has a dual role: signal transduction from the type III secretion system needle tip and intracellular secretion regulation. |
Q92968788 | Shigella-mediated immunosuppression in the human gut: subversion extends from innate to adaptive immune responses |
Q57048274 | SsaV Interacts with SsaL to Control the Translocon-to-Effector Switch in the SPI-2 Type Three Secretion System |
Q42324204 | Steps for Shigella Gatekeeper Protein MxiC Function in Hierarchical Type III Secretion Regulation. |
Q40442116 | Structural analysis of SepL, an enteropathogenic Escherichia coli type III secretion-system gatekeeper protein |
Q38006509 | Surface organelles assembled by secretion systems of Gram-negative bacteria: diversity in structure and function |
Q40522214 | The Architecture of the Cytoplasmic Region of Type III Secretion Systems |
Q47744378 | The Pseudomonas syringae HrpJ protein controls the secretion of type III translocator proteins and has a virulence role inside plant cells |
Q35972461 | The Type III Secretion Translocation Pore Senses Host Cell Contact. |
Q28488627 | The common structural architecture of Shigella flexneri and Salmonella typhimurium type three secretion needles |
Q47341878 | The inner-rod component of Shigella flexneri type 3 secretion system, MxiI, is involved in the transmission of the secretion activation signal by its interaction with MxiC. |
Q42566246 | Three-dimensional electron microscopy reconstruction and cysteine-mediated crosslinking provide a model of the type III secretion system needle tip complex. |
Q38586932 | Type III secretion systems: the bacterial flagellum and the injectisome |
Q28074332 | Type Three Secretion System in Attaching and Effacing Pathogens |
Q90451358 | Vibrio parahaemolyticus Senses Intracellular K+ To Translocate Type III Secretion System 2 Effectors Effectively |
Q41405474 | YopK controls both rate and fidelity of Yop translocation |
Q40603864 | YopN and TyeA Hydrophobic Contacts Required for Regulating Ysc-Yop Type III Secretion Activity by Yersinia pseudotuberculosis |
Q54212107 | YopN is required for efficient effector translocation and virulence in Yersinia pseudotuberculosis. |
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