review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Paul O'Toole | Q39051364 |
P2093 | author name string | Kieran A Ryan | |
Richard C Waters | |||
P2860 | cites work | CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 |
The bacterial flagellum: reversible rotary propellor and type III export apparatus | Q24516868 | ||
Bacterial flagella rotating in bundles: a study in helical geometry | Q24602599 | ||
Complete atomic model of the bacterial flagellar filament by electron cryomicroscopy | Q27641789 | ||
Gene array analysis of Yersinia enterocolitica FlhD and FlhC: regulation of enzymes affecting synthesis and degradation of carbamoylphosphate | Q38338823 | ||
Genome-wide analysis of transcriptional hierarchy and feedback regulation in the flagellar system of Helicobacter pylori | Q38341547 | ||
The three-dimensional structure of the flagellar rotor from a clockwise-locked mutant of Salmonella enterica serovar Typhimurium | Q39110183 | ||
Helicobacter pylori FlhB function: the FlhB C-terminal homologue HP1575 acts as a "spare part" to permit flagellar export when the HP0770 FlhBCC domain is deleted | Q39110631 | ||
Uncovering a large set of genes that affect surface motility in Salmonella enterica serovar Typhimurium | Q39112479 | ||
A new fla gene in Salmonella typhimurium--flaR--and its mutant phenotype-superhooks | Q50235168 | ||
A cell division regulatory mechanism controls the flagellar regulon in Escherichia coli. | Q54732237 | ||
Determination of bacteriophage λ tail length by a protein ruler | Q59098445 | ||
Translation of the UGA triplet in vitro by tryptophan transfer RNA's | Q69938785 | ||
Length determination in bacteriophage lambda tails | Q72405349 | ||
Peptide display on bacterial flagella: principles and applications | Q28144560 | ||
Evidence that nebulin is a protein-ruler in muscle thin filaments | Q28278748 | ||
YscP of Yersinia pestis is a secreted component of the Yop secretion system | Q28492821 | ||
Bacterial flagellar diversity in the post-genomic era. | Q30986724 | ||
The cytoplasmic component of the bacterial flagellar motor | Q33611845 | ||
How Bacteria Assemble Flagella | Q34194719 | ||
Flagellar rotation and the mechanism of bacterial motility | Q34214225 | ||
Export of an N-terminal fragment of Escherichia coli flagellin by a flagellum-specific pathway | Q34285883 | ||
Spa32 regulates a switch in substrate specificity of the type III secreton of Shigella flexneri from needle components to Ipa proteins | Q34314419 | ||
The needle length of bacterial injectisomes is determined by a molecular ruler. | Q34543727 | ||
Novel conserved assembly factor of the bacterial flagellum. | Q34560923 | ||
FlhD/FlhC is a regulator of anaerobic respiration and the Entner-Doudoroff pathway through induction of the methyl-accepting chemotaxis protein Aer. | Q34580405 | ||
Flagellin perception: a paradigm for innate immunity | Q34671311 | ||
Toll-like receptor-5 and the innate immune response to bacterial flagellin. | Q35017544 | ||
The rotary motor of bacterial flagella | Q35034069 | ||
ASSEMBLY AND STABILITY OF THE TOBACCO MOSAIC VIRUS PARTICLE. | Q35442271 | ||
Characterization of the flagellar hook length control protein fliK of Salmonella typhimurium and Escherichia coli | Q35607613 | ||
Hook-length control of the export-switching machinery involves a double-locked gate in Salmonella typhimurium flagellar morphogenesis | Q35620045 | ||
Genetics and biogenesis of bacterial flagella | Q35656714 | ||
Conserved features of type III secretion | Q35845019 | ||
Process of protein transport by the type III secretion system | Q35980175 | ||
Genetic and biochemical analysis of the flagellar hook of Treponema phagedenis | Q36108429 | ||
Biochemical and antigenic properties of the Campylobacter flagellar hook protein | Q36112431 | ||
Identification and characterization of the products of six region III flagellar genes (flaAII.3 through flaQII) of Salmonella typhimurium | Q36202813 | ||
Role of the flaR gene in flagellar hook formation in Salmonella spp | Q36309220 | ||
Role of gene flaFV on flagellar hook formation in Salmonella typhimurium | Q36313338 | ||
Incomplete flagellar structures in Escherichia coli mutants | Q36322064 | ||
Identification of the structural gene for the hook subunit protein of Escherichia coli flagella | Q36417729 | ||
Fine Structure and Isolation of the Hook-Basal Body Complex of Flagella from Escherichia coli and Bacillus subtilis | Q36539726 | ||
Flipping the switch: bringing order to flagellar assembly | Q36635739 | ||
Non-motile mutants of Helicobacter pylori and Helicobacter mustelae defective in flagellar hook production. | Q36719850 | ||
Differentiation within the bacterial flagellum and isolation of the proximal hook | Q36825137 | ||
Structural and genetic analysis of a mutant of Rhodobacter sphaeroides WS8 deficient in hook length control | Q36888892 | ||
Transfer ribonucleic acid-mediated suppression of termination codons in Escherichia coli | Q37064483 | ||
Flagellar hook protein from Salmonella SJ25. | Q39360693 | ||
Components of the Salmonella flagellar export apparatus and classification of export substrates | Q39494402 | ||
Effect of hook subunit concentration on assembly and control of length of the flagellar hook of Salmonella | Q39497567 | ||
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 | ||
Domain structure of Salmonella FlhB, a flagellar export component responsible for substrate specificity switching | Q39587747 | ||
Isolation and characterization of bacterial flagellar hook proteins from salmonellae and Escherichia coli | Q39660459 | ||
Shigella Spa32 is an essential secretory protein for functional type III secretion machinery and uniformity of its needle length | Q39678365 | ||
Flagellum-mediated adhesion by Burkholderia pseudomallei precedes invasion of Acanthamoeba astronyxis | Q39741698 | ||
The ATPase FliI can interact with the type III flagellar protein export apparatus in the absence of its regulator, FliH. | Q39775119 | ||
Mutations in fliK and flhB affecting flagellar hook and filament assembly in Salmonella typhimurium | Q39841418 | ||
Roles of FliK and FlhB in determination of flagellar hook length in Salmonella typhimurium | Q39897839 | ||
Isolation and characterization of FliK-independent flagellation mutants from Salmonella typhimurium | Q39899605 | ||
FlgD is a scaffolding protein needed for flagellar hook assembly in Salmonella typhimurium | Q39931449 | ||
Multiple factors underlying the maximum motility of Escherichia coli as cultures enter post-exponential growth | Q39937159 | ||
Transcriptional analysis of the flagellar regulon of Salmonella typhimurium | Q39943833 | ||
Incomplete flagellar structures in nonflagellate mutants of Salmonella typhimurium | Q39989881 | ||
Kinetic analysis of the growth rate of the flagellar hook in Salmonella typhimurium by the population balance method | Q40114043 | ||
Aeromonas flagella (polar and lateral) are enterocyte adhesins that contribute to biofilm formation on surfaces | Q40574790 | ||
Characterization of a Type III secretion substrate specificity switch (T3S4) domain in YscP from Yersinia enterocolitica. | Q41459145 | ||
YscP, a Yersinia protein required for Yop secretion that is surface exposed, and released in low Ca2+. | Q41478484 | ||
MotD of Sinorhizobium meliloti and related alpha-proteobacteria is the flagellar-hook-length regulator and therefore reassigned as FliK. | Q41821295 | ||
Binding and transcriptional activation of non-flagellar genes by the Escherichia coli flagellar master regulator FlhD2C2. | Q42286761 | ||
Intrinsic membrane targeting of the flagellar export ATPase FliI: interaction with acidic phospholipids and FliH. | Q42425520 | ||
Purification and characterization of the flagellar hook-basal body complex of Bacillus subtilis | Q42438682 | ||
The FliP and FliR proteins of Salmonella typhimurium, putative components of the type III flagellar export apparatus, are located in the flagellar basal body | Q42449241 | ||
Structure of the rotor of the bacterial flagellar motor revealed by electron cryomicroscopy and single-particle image analysis | Q42458039 | ||
Domain organization and function of Salmonella FliK, a flagellar hook-length control protein | Q42465335 | ||
Interactions among components of the Salmonella flagellar export apparatus and its substrates | Q42484827 | ||
Information essential for cell-cycle-dependent secretion of the 591-residue Caulobacter hook protein is confined to a 21-amino-acid sequence near the N-terminus | Q42488271 | ||
Helicobacter pylori flagellar hook-filament transition is controlled by a FliK functional homolog encoded by the gene HP0906. | Q42949037 | ||
Interactions among membrane and soluble components of the flagellar export apparatus of Salmonella | Q44075139 | ||
FlhB regulates ordered export of flagellar components via autocleavage mechanism | Q47844679 | ||
Two parts of the T3S4 domain of the hook-length control protein FliK are essential for the substrate specificity switching of the flagellar type III export apparatus | Q50077374 | ||
The type III flagellar export specificity switch is dependent on FliK ruler and a molecular clock | Q50081632 | ||
N-terminal signal region of FliK is dispensable for length control of the flagellar hook | Q50091919 | ||
Substrate specificity of type III flagellar protein export in Salmonella is controlled by subdomain interactions in FlhB. | Q50103898 | ||
Length of the flagellar hook and the capacity of the type III export apparatus | Q50116307 | ||
FliH, a soluble component of the type III flagellar export apparatus of Salmonella, forms a complex with FliI and inhibits its ATPase activity | Q50119364 | ||
Flagellar proteins and type III-exported virulence factors are the predominant proteins secreted into the culture media of Salmonella typhimurium | Q50123650 | ||
FliK, the protein responsible for flagellar hook length control in Salmonella, is exported during hook assembly | Q50123674 | ||
Effect of cellular level of FliK on flagellar hook and filament assembly in Salmonella typhimurium | Q50130992 | ||
Enzymatic characterization of FliI. An ATPase involved in flagellar assembly in Salmonella typhimurium | Q50136458 | ||
Molecular dissection of the flagellum-specific anti-sigma factor, FlgM, of Salmonella typhimurium | Q50141336 | ||
Isolation, characterization and structure of bacterial flagellar motors containing the switch complex | Q50152418 | ||
Morphological pathway of flagellar assembly in Salmonella typhimurium | Q50175027 | ||
Reconstruction in vitro of the flagellar polyhook from Salmonella | Q50212885 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 769-780 | |
P577 | publication date | 2007-05-01 | |
P1433 | published in | Protein Science | Q7251445 |
P1476 | title | The FliK protein and flagellar hook-length control | |
P478 | volume | 16 |
Q54324587 | A new highly discriminatory multiplex capillary-based MLVA assay as a tool for the epidemiological survey of Pseudomonas aeruginosa in cystic fibrosis patients. |
Q37165158 | Coordinating assembly of a bacterial macromolecular machine |
Q95325037 | Detecting qualitative changes in biological systems |
Q35193316 | Differential single nucleotide polymorphism-based analysis of an outbreak caused by Salmonella enterica serovar Manhattan reveals epidemiological details missed by standard pulsed-field gel electrophoresis |
Q54348779 | EscI: a crucial component of the type III secretion system forms the inner rod structure in enteropathogenic Escherichia coli. |
Q37350406 | Flagellar motility in bacteria structure and function of flagellar motor |
Q30318400 | Functional characterization of the type III secretion substrate specificity switch protein HpaC from Xanthomonas campestris pv. vesicatoria |
Q61800931 | Genomic analyses of two Alteromonas stellipolaris strains reveal traits with potential biotechnological applications |
Q30319509 | HpaC controls substrate specificity of the Xanthomonas type III secretion system |
Q37125371 | Identification and characterization of a novel flagellum-dependent Salmonella-infecting bacteriophage, iEPS5 |
Q91386905 | In vivo structure of the Legionella type II secretion system by electron cryotomography |
Q36197586 | Mystery of fliK in length control of the flagellar hook |
Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
Q36197603 | Rebuttal: flagellar hook length is controlled by a secreted molecular ruler |
Q34390820 | Reduced set of virulence genes allows high accuracy prediction of bacterial pathogenicity in humans |
Q36363508 | Role of EscP (Orf16) in injectisome biogenesis and regulation of type III protein secretion in enteropathogenic Escherichia coli |
Q38928178 | Role of the Flagellar Hook-Length Control Protein FliK and σ28 in cagA Expression in Gastric Cell-Adhered Helicobacter pylori |
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. |
Q33637917 | Sense and sensibility: flagellum-mediated gene regulation |
Q30724599 | Species-dependent hydrodynamics of flagellum-tethered bacteria in early biofilm development |
Q38454417 | The role of probiotics in the inhibition of Campylobacter jejuni colonization and virulence attenuation |
Q37156434 | The surprisingly diverse ways that prokaryotes move |
Q37665331 | Timing is everything: the regulation of type III secretion |
Q28074332 | Type Three Secretion System in Attaching and Effacing Pathogens |
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