| scholarly article | Q13442814 |
| P50 | author | Victor Sourjik | Q60948993 |
| P2093 | author name string | Hui Li | |
| P2860 | cites work | Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection | Q22122301 |
| Localization of the Salmonella typhimurium flagellar switch protein FliG to the cytoplasmic M-ring face of the basal body | Q24564620 | ||
| The c-di-GMP binding protein YcgR controls flagellar motor direction and speed to affect chemotaxis by a "backstop brake" mechanism | Q24624328 | ||
| A comprehensive genetic characterization of bacterial motility | Q27314864 | ||
| Structure of the cytoplasmic domain of FlhA and implication for flagellar type III protein export | Q27660101 | ||
| FlhA provides the adaptor for coordinated delivery of late flagella building blocks to the type III secretion system | Q27662152 | ||
| The complete genome sequence of Escherichia coli K-12 | Q27860542 | ||
| One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
| Dependence of bacterial chemotaxis on gradient shape and adaptation rate | Q28304568 | ||
| Structure of FliM provides insight into assembly of the switch complex in the bacterial flagella motor | Q28485426 | ||
| Overproduction of the bacterial flagellar switch proteins and their interactions with the MS ring complex in vitro | Q28490085 | ||
| Role of the C-terminal cytoplasmic domain of FlhA in bacterial flagellar type III protein export | Q28563581 | ||
| Mutational analysis of the flagellar protein FliG: sites of interaction with FliM and implications for organization of the switch complex | Q28763609 | ||
| Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells | Q29547331 | ||
| Crystal structure of the flagellar rotor protein FliN from Thermotoga maritima | Q30475802 | ||
| Organization of FliN subunits in the flagellar motor of Escherichia coli | Q30477115 | ||
| FliH, a soluble component of the type III flagellar export apparatus of Salmonella, forms a complex with FliI and inhibits its ATPase activity | Q50119364 | ||
| Distinct regions of bacterial flagellar switch protein FliM interact with FliG, FliN and CheY. | Q50132978 | ||
| Morphological pathway of flagellar assembly in Salmonella typhimurium | Q50175027 | ||
| Exchange of rotor components in functioning bacterial flagellar motor. | Q50561923 | ||
| In vivo measurement by FRET of pathway activity in bacterial chemotaxis. | Q50674661 | ||
| Determinants of chemoreceptor cluster formation in Escherichia coli. | Q54459232 | ||
| Design principles of a bacterial signalling network | Q56637295 | ||
| Mutational analysis of the flagellar rotor protein FliN: identification of surfaces important for flagellar assembly and switching | Q30477806 | ||
| The bacterial flagellar switch complex is getting more complex | Q30481718 | ||
| Transient response to chemotactic stimuli in Escherichia coli | Q30941323 | ||
| Stoichiometry and turnover in single, functioning membrane protein complexes. | Q33257539 | ||
| Structures of bacterial flagellar motors from two FliF-FliG gene fusion mutants | Q33554942 | ||
| Signal-dependent turnover of the bacterial flagellar switch protein FliM. | Q33953248 | ||
| Variable symmetry in Salmonella typhimurium flagellar motors | Q34180232 | ||
| How Bacteria Assemble Flagella | Q34194719 | ||
| In situ structure of the complete Treponema primitia flagellar motor | Q34553794 | ||
| The PilZ domain is a receptor for the second messenger c-di-GMP: the PilZ domain protein YcgR controls motility in enterobacteria | Q34559000 | ||
| Heat-shock proteins | Q34773635 | ||
| Mechanisms of type III protein export for bacterial flagellar assembly. | Q34860251 | ||
| The rotary motor of bacterial flagella | Q35034069 | ||
| C-ring requirement in flagellar type III secretion is bypassed by FlhDC upregulation. | Q35357107 | ||
| Torque generation in the flagellar motor of Escherichia coli: evidence of a direct role for FliG but not for FliM or FliN. | Q35600586 | ||
| FliG and FliM distribution in the Salmonella typhimurium cell and flagellar basal bodies | Q35600631 | ||
| Rotational symmetry of the C ring and a mechanism for the flagellar rotary motor | Q35617047 | ||
| Protein exchange dynamics at chemoreceptor clusters in Escherichia coli | Q36609149 | ||
| Dynamic map of protein interactions in the Escherichia coli chemotaxis pathway | Q37101011 | ||
| Molecular motors of the bacterial flagella | Q37291882 | ||
| Geometry of the flagellar motor in the cytoplasmic membrane of Salmonella typhimurium as determined by stereo-photogrammetry of quick-freeze deep-etch replica images | Q39418662 | ||
| 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 | ||
| Flagellar assembly in Salmonella typhimurium | Q41121961 | ||
| FlgB, FlgC, FlgF and FlgG. A family of structurally related proteins in the flagellar basal body of Salmonella typhimurium | Q41196112 | ||
| 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 | ||
| M ring, S ring and proximal rod of the flagellar basal body of Salmonella typhimurium are composed of subunits of a single protein, FliF. | Q42455767 | ||
| Structure of the rotor of the bacterial flagellar motor revealed by electron cryomicroscopy and single-particle image analysis | Q42458039 | ||
| Roles of the extreme N-terminal region of FliH for efficient localization of the FliH-FliI complex to the bacterial flagellar type III export apparatus. | Q42462440 | ||
| Stoichiometric analysis of the flagellar hook-(basal-body) complex of Salmonella typhimurium | Q42481113 | ||
| The FliN-FliH interaction mediates localization of flagellar export ATPase FliI to the C ring complex | Q42501832 | ||
| Visualization of functional rotor proteins of the bacterial flagellar motor in the cell membrane | Q42508070 | ||
| Second messenger-mediated adjustment of bacterial swimming velocity | Q44130151 | ||
| Gene replacement without selection: regulated suppression of amber mutations in Escherichia coli | Q44508201 | ||
| Solubilization and purification of the MotA/MotB complex of Escherichia coli | Q44713865 | ||
| 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 | ||
| FliL is essential for swarming: motor rotation in absence of FliL fractures the flagellar rod in swarmer cells of Salmonella enterica | Q50064025 | ||
| Interactions between C ring proteins and export apparatus components: a possible mechanism for facilitating type III protein export | Q50081214 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Escherichia coli | Q25419 |
| P304 | page(s) | 886-899 | |
| P577 | publication date | 2011-02-10 | |
| P1433 | published in | Molecular Microbiology | Q6895967 |
| P1476 | title | Assembly and stability of flagellar motor in Escherichia coli | |
| P478 | volume | 80 |
| Q90008011 | A Polar Flagellar Transcriptional Program Mediated by Diverse Two-Component Signal Transduction Systems and Basal Flagellar Proteins Is Broadly Conserved in Polar Flagellates |
| Q35100513 | A Salmonella type three secretion effector/chaperone complex adopts a hexameric ring-like structure |
| Q40108388 | A flagellum-specific chaperone facilitates assembly of the core type III export apparatus of the bacterial flagellum |
| Q35172343 | A new player at the flagellar motor: FliL controls both motor output and bias |
| Q43126063 | A novel dnaJ family gene, sflA, encodes an inhibitor of flagellation in marine Vibrio species |
| Q41950585 | A regulatory checkpoint during flagellar biogenesis in Campylobacter jejuni initiates signal transduction to activate transcription of flagellar genes. |
| Q34115643 | Adaptive remodelling by FliN in the bacterial rotary motor |
| Q35362432 | Adjusting the spokes of the flagellar motor with the DNA-binding protein H-NS. |
| Q27675415 | Architecture of the major component of the type III secretion system export apparatus |
| Q42452873 | Assembly and stoichiometry of FliF and FlhA in Salmonella flagellar basal body |
| Q30588899 | Assembly dynamics and the roles of FliI ATPase of the bacterial flagellar export apparatus. |
| Q41411817 | Assembly of the Yersinia injectisome: the missing pieces. |
| Q38183945 | Assembly of the bacterial type III secretion machinery. |
| Q38563463 | Bacterial protein networks: properties and functions |
| Q35572991 | Basal Body Structures Differentially Affect Transcription of RpoN- and FliA-Dependent Flagellar Genes in Helicobacter pylori. |
| Q42511166 | Biogenesis of the Flagellar Switch Complex in Escherichia coli: Formation of Sub-Complexes Independently of the Basal-Body MS-Ring |
| Q40194202 | Characterisation of Shigella Spa33 and Thermotoga FliM/N reveals a new model for C-ring assembly in T3SS. |
| Q41185215 | Characterization of the flagellar motor composed of functional GFP-fusion derivatives of FliG in the Na+-driven polar flagellum of Vibrio alginolyticus |
| Q27313367 | Composition, formation, and regulation of the cytosolic c-ring, a dynamic component of the type III secretion injectisome |
| Q34304629 | Counting single photoactivatable fluorescent molecules by photoactivated localization microscopy (PALM). |
| Q43187793 | Energy complexes are apparently associated with the switch-motor complex of bacterial flagella |
| Q37218224 | Escherichia coli Type III Secretion System 2 ATPase EivC Is Involved in the Motility and Virulence of Avian Pathogenic Escherichia coli |
| Q26858982 | Expanded roles for multicargo and class 1B effector chaperones in type III secretion |
| Q52340379 | Experimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate. |
| Q42018644 | Flagellar biosynthesis exerts temporal regulation of secretion of specific Campylobacter jejuni colonization and virulence determinants |
| Q34486085 | Function of the Histone-Like Protein H-NS in Motility of Escherichia coli: Multiple Regulatory Roles Rather than Direct Action at the Flagellar Motor |
| Q42187679 | Functional Activation of the Flagellar Type III Secretion Export Apparatus |
| Q28490001 | Functional characterization of the type III secretion ATPase SsaN encoded by Salmonella pathogenicity island 2 |
| Q41227013 | Genetic analysis of revertants isolated from the rod-fragile fliF mutant of Salmonella |
| Q34845890 | Genome-scale co-evolutionary inference identifies functions and clients of bacterial Hsp90 |
| Q39629464 | GerM is required to assemble the basal platform of the SpoIIIA-SpoIIQ transenvelope complex during sporulation in Bacillus subtilis |
| Q28084721 | How bacteria maintain location and number of flagella? |
| Q92565279 | Inefficient Secretion of Anti-sigma Factor FlgM Inhibits Bacterial Motility at High Temperature |
| Q43098514 | Interaction of the C-terminal tail of FliF with FliG from the Na+-driven flagellar motor of Vibrio alginolyticus |
| Q51302841 | Living on the edge: emergence of spontaneous gac mutations in Pseudomonas protegens during swarming motility. |
| Q34888231 | Loss of FliL alters Proteus mirabilis surface sensing and temperature-dependent swarming |
| Q36471163 | Mechanism for adaptive remodeling of the bacterial flagellar switch. |
| Q35668113 | Perturbation of FliL interferes with Proteus mirabilis swarmer cell gene expression and differentiation |
| Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
| Q33989031 | SecDF as part of the Sec-translocase facilitates efficient secretion of Bacillus cereus toxins and cell wall-associated proteins |
| Q28069668 | Shedding light on biology of bacterial cells |
| Q89793934 | Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli |
| Q34165357 | Stoichiometry and turnover of the bacterial flagellar switch protein FliN. |
| Q57073743 | Switching and Torque Generation in Swarming |
| Q35221714 | Switching of bacterial flagellar motors [corrected] triggered by mutant FliG. |
| Q40614480 | The Bacterial Stress-Responsive Hsp90 Chaperone (HtpG) Is Required for the Production of the Genotoxin Colibactin and the Siderophore Yersiniabactin in Escherichia coli |
| Q41425944 | The assembly of the export apparatus (YscR,S,T,U,V) of the Yersinia type III secretion apparatus occurs independently of other structural components and involves the formation of an YscV oligomer. |
| Q35023354 | The sensory histidine kinases TorS and EvgS tend to form clusters in Escherichia coli cells |
| Q38253935 | The structure and regulation of flagella in Bacillus subtilis |
| Q90315532 | TnFLX: a third-generation mariner-based transposon system for Bacillus subtilis |
| Q41484286 | Transcriptional control of motility enables directional movement of Escherichia coli in a signal gradient. |
| Q38586932 | Type III secretion systems: the bacterial flagellum and the injectisome |
| Q37388926 | c-di-GMP heterogeneity is generated by the chemotaxis machinery to regulate flagellar motility |
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