scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1022215472 |
P356 | DOI | 10.1186/1471-2180-10-18 |
P932 | PMC publication ID | 2830194 |
P698 | PubMed publication ID | 20096108 |
P5875 | ResearchGate publication ID | 41121498 |
P2093 | author name string | James B Mahony | |
Chris B Stone | |||
David C Bulir | |||
Jodi D Gilchrist | |||
Raman K Toor | |||
P2860 | cites work | Intergenic suppression between the flagellar MS ring protein FliF of Salmonella and FlhA, a membrane component of its export apparatus | Q39502769 |
Role of FliJ in flagellar protein export in Salmonella | Q39538800 | ||
Interactions of FliJ with the Salmonella type III flagellar export apparatus | Q39887119 | ||
Cross talk between type III secretion and flagellar assembly systems in Pseudomonas aeruginosa. | Q40169819 | ||
Interactions among components of the Salmonella flagellar export apparatus and its substrates | Q42484827 | ||
Energy source of flagellar type III secretion | Q46793602 | ||
Distinct roles of the FliI ATPase and proton motive force in bacterial flagellar protein export | Q46793605 | ||
Interacting components of the flagellar motor of Escherichia coli revealed by the two-hybrid system in yeast | Q48066024 | ||
FliH, a soluble component of the type III flagellar export apparatus of Salmonella, forms a complex with FliI and inhibits its ATPase activity | Q50119364 | ||
Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium | Q50136458 | ||
Morphological pathway of flagellar assembly in Salmonella typhimurium | Q50175027 | ||
Enzymatic characterization of the enteropathogenic Escherichia coli type III secretion ATPase EscN. | Q54432108 | ||
Role of the N-terminal domain of FliI ATPase in bacterial flagellar protein export | Q57174429 | ||
Comparative genomes of Chlamydia pneumoniae and C. trachomatis | Q22122313 | ||
A chlamydial type III translocated protein is tyrosine-phosphorylated at the site of entry and associated with recruitment of actin | Q24564460 | ||
Structural similarity between the flagellar type III ATPase FliI and F1-ATPase subunits | Q27641045 | ||
Bacterial flagella and type III secretion systems | Q28214315 | ||
Chaperone release and unfolding of substrates in type III secretion | Q28275782 | ||
Analysis of the cytoplasmic domains of Salmonella FlhA and interactions with components of the flagellar export machinery | Q28770106 | ||
Mechanisms of host cell exit by the intracellular bacterium Chlamydia | Q30480273 | ||
Spatial constraints within the chlamydial host cell inclusion predict interrupted development and persistence | Q33313651 | ||
Chlamydial entry involves TARP binding of guanine nucleotide exchange factors | Q33326689 | ||
Interaction network among Escherichia coli membrane proteins involved in cell division as revealed by bacterial two-hybrid analysis | Q33716640 | ||
Background and current knowledge of Chlamydia pneumoniae and atherosclerosis | Q33935003 | ||
Role of FliF and FliI of Listeria monocytogenes in flagellar assembly and pathogenicity | Q34033803 | ||
The chlamydial inclusion preferentially intercepts basolaterally directed sphingomyelin-containing exocytic vacuoles. | Q34180608 | ||
Requirement of flhA for swarming differentiation, flagellin export, and secretion of virulence-associated proteins in Bacillus thuringiensis | Q34320687 | ||
Evolutionary links between FliH/YscL-like proteins from bacterial type III secretion systems and second-stalk components of the FoF1 and vacuolar ATPases | Q34500271 | ||
Chlamydia pneumoniae as a respiratory pathogen | Q34542090 | ||
Characterization of the Yersinia enterocolitica type III secretion ATPase YscN and its regulator, YscL. | Q34696832 | ||
The rotary motor of bacterial flagella | Q35034069 | ||
YscU cleavage and the assembly of Yersinia type III secretion machine complexes | Q36513832 | ||
Utilization of L-cell nucleoside triphosphates by Chlamydia psittaci for ribonucleic acid synthesis | Q36763048 | ||
Type III secretion à la Chlamydia | Q36812549 | ||
Interaction of chlamydiae and host cells in vitro | Q37056842 | ||
Chlamydophila pneumoniae and the etiology of late-onset Alzheimer's disease | Q37167099 | ||
Chlamydia causes fragmentation of the Golgi compartment to ensure reproduction. | Q37856042 | ||
Characterization of the putative type III secretion ATPase CdsN (Cpn0707) of Chlamydophila pneumoniae | Q37856790 | ||
Interactions between CdsD, CdsQ, and CdsL, three putative Chlamydophila pneumoniae type III secretion proteins | Q37858039 | ||
Chlamydia pneumoniae arthritis in a patient with common variable immunodeficiency. | Q37864940 | ||
Identification of MEK- and phosphoinositide 3-kinase-dependent signalling as essential events during Chlamydia pneumoniae invasion of HEp2 cells | Q37871641 | ||
Mammalian 14-3-3beta associates with the Chlamydia trachomatis inclusion membrane via its interaction with IncG. | Q37874599 | ||
Evidence for the secretion of Chlamydia trachomatis CopN by a type III secretion mechanism. | Q37875136 | ||
Host cell phospholipids are trafficked to and then modified by Chlamydia trachomatis | Q37881941 | ||
P921 | main subject | Chlamydia pneumoniae | Q62869737 |
P304 | page(s) | 18 | |
P577 | publication date | 2010-01-22 | |
P1433 | published in | BMC Microbiology | Q15759430 |
P1476 | title | Interactions between flagellar and type III secretion proteins in Chlamydia pneumoniae | |
P478 | volume | 10 |
Q36594034 | A working model for the type III secretion mechanism in Chlamydia |
Q38183945 | Assembly of the bacterial type III secretion machinery. |
Q21266688 | Construction of a highly flexible and comprehensive gene collection representing the ORFeome of the human pathogen Chlamydia pneumoniae |
Q33617984 | Diversity of secretion systems associated with virulence characteristics of the classical bordetellae |
Q37839872 | Hypothetical protein CT398 (CdsZ) interacts with σ(54) (RpoN)-holoenzyme and the type III secretion export apparatus in Chlamydia trachomatis |
Q40364421 | Mechanism of type-III protein secretion: Regulation of FlhA conformation by a functionally critical charged-residue cluster. |
Q37548120 | New frontiers in type III secretion biology: the Chlamydia perspective |
Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
Q40413291 | Spa47 is an oligomerization-activated type three secretion system (T3SS) ATPase from Shigella flexneri |
Q36623002 | Structural modeling of the flagellum MS ring protein FliF reveals similarities to the type III secretion system and sporulation complex |
Q27661313 | Structure of the Cytoplasmic Domain of the Flagellar Secretion Apparatus Component FlhA from Helicobacter pylori |
Q37367260 | The Aeromonas salmonicida subsp. salmonicida exoproteome: determination of the complete repertoire of Type-Three Secretion System effectors and identification of other virulence factors |
Q35075114 | The Chlamydial Type III Secretion Mechanism: Revealing Cracks in a Tough Nut. |
Q37508088 | The chlamydiales pangenome revisited: structural stability and functional coherence |
Q37833909 | Unexpected genomic features in widespread intracellular bacteria: evidence for motility of marine chlamydiae |
Q35639106 | Unity in variety--the pan-genome of the Chlamydiae |
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