| scholarly article | Q13442814 |
| P356 | DOI | 10.1128/JB.179.19.6092-6099.1997 |
| P8608 | Fatcat ID | release_esibgwqexjap7d26ohdlv34xnm |
| P932 | PMC publication ID | 179513 |
| P698 | PubMed publication ID | 9324257 |
| P2093 | author name string | R M Macnab | |
| M Kihara | |||
| F Fan | |||
| K Ohnishi | |||
| G J Schoenhals | |||
| P2860 | cites work | The end of the line in bacterial sensing: the flagellar motor | Q39578918 |
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| The hrp gene locus of Pseudomonas solanacearum, which controls the production of a type III secretion system, encodes eight proteins related to components of the bacterial flagellar biogenesis complex. | Q41495226 | ||
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| Bacillus subtilis flagellar proteins FliP, FliQ, FliR and FlhB are related to Shigella flexneri virulence factors | Q48087031 | ||
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| Genetic Analysis of H2, the Structural Gene for Phase-2 Flagellin in Salmonella | Q50209142 | ||
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| Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes | Q27860623 | ||
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| Salmonella typhimurium mutants defective in flagellar filament regrowth and sequence similarity of FliI to F0F1, vacuolar, and archaebacterial ATPase subunits | Q33233253 | ||
| Identifying nonpolar transbilayer helices in amino acid sequences of membrane proteins | Q34181973 | ||
| Recognition of protein coding regions in DNA sequences | Q35528942 | ||
| Characterization of the flagellar hook length control protein fliK of Salmonella typhimurium and Escherichia coli | Q35607613 | ||
| Characterization of the fliE genes of Escherichia coli and Salmonella typhimurium and identification of the FliE protein as a component of the flagellar hook-basal body complex | Q36110603 | ||
| RcsA, an unstable positive regulator of capsular polysaccharide synthesis | Q36131598 | ||
| L-, P-, and M-ring proteins of the flagellar basal body of Salmonella typhimurium: gene sequences and deduced protein sequences | Q36179875 | ||
| Overproduction of the MotA protein of Escherichia coli and estimation of its wild-type level | Q36187867 | ||
| Identification and characterization of the products of six region III flagellar genes (flaAII.3 through flaQII) of Salmonella typhimurium | Q36202813 | ||
| Subunit II of cytochrome c oxidase from Paracoccus denitrificans. DNA sequence, gene expression and the protein | Q36282312 | ||
| Incomplete flagellar structures in Escherichia coli mutants | Q36322064 | ||
| P433 | issue | 19 | |
| P921 | main subject | Salmonella Typhimurium | Q166491 |
| P304 | page(s) | 6092-6099 | |
| P577 | publication date | 1997-10-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | The FliO, FliP, FliQ, and FliR proteins of Salmonella typhimurium: putative components for flagellar assembly | |
| P478 | volume | 179 |
| Q40108388 | A flagellum-specific chaperone facilitates assembly of the core type III export apparatus of the bacterial flagellum |
| Q33813527 | Abrogation of the twin arginine transport system in Salmonella enterica serovar Typhimurium leads to colonization defects during infection |
| Q35768702 | An escort mechanism for cycling of export chaperones during flagellum assembly |
| Q42609960 | An intrinsically disordered linker controlling the formation and the stability of the bacterial flagellar hook |
| Q40867738 | Analysis of an engineered Salmonella flagellar fusion protein, FliR-FlhB. |
| Q39566457 | Analysis of genes involved in biosynthesis of coronafacic acid, the polyketide component of the phytotoxin coronatine. |
| Q28770106 | Analysis of the cytoplasmic domains of Salmonella FlhA and interactions with components of the flagellar export machinery |
| Q30603453 | Assembling flagella in Salmonella mutant strains producing a type III export apparatus without FliO. |
| Q40108405 | Assembly and stoichiometry of the core structure of the bacterial flagellar type III export gate complex. |
| Q38183945 | Assembly of the bacterial type III secretion machinery. |
| Q42466808 | Bacterial flagellation and cell division |
| Q39494402 | Components of the Salmonella flagellar export apparatus and classification of export substrates |
| Q33932463 | Constraints on models for the flagellar rotary motor |
| Q30463935 | Cross-complementation study of the flagellar type III export apparatus membrane protein FlhB |
| Q41995741 | Crystallization and preliminary X-ray analysis of the periplasmic domain of FliP, an integral membrane component of the bacterial flagellar type III protein-export apparatus |
| Q33326978 | Deciphering interplay between Salmonella invasion effectors |
| Q40600401 | EscO, a functional and structural analog of the flagellar FliJ protein, is a positive regulator of EscN ATPase activity of the enteropathogenic Escherichia coli injectisome |
| Q41832635 | Flagellar formation in C-ring-defective mutants by overproduction of FliI, the ATPase specific for flagellar type III secretion |
| Q47844679 | FlhB regulates ordered export of flagellar components via autocleavage mechanism |
| Q36999741 | FliH and FliI ensure efficient energy coupling of flagellar type III protein export in Salmonella. |
| Q41448695 | FliK regulates flagellar hook length as an internal ruler |
| Q33717044 | FliO Regulation of FliP in the Formation of the Salmonella enterica Flagellum |
| Q49953367 | Fuel of the Bacterial Flagellar Type III Protein Export Apparatus |
| Q34848296 | Function of FlhB, a membrane protein implicated in the bacterial flagellar type III secretion system |
| Q49972596 | Function of the conserved FHIPEP domain of the flagellar type III export apparatus, protein FlhA. |
| Q42187679 | Functional Activation of the Flagellar Type III Secretion Export Apparatus |
| Q49209853 | Fungal networks shape dynamics of bacterial dispersal and community assembly in cheese rind microbiomes |
| Q46471134 | Geobacter sulfurreducens strain engineered for increased rates of respiration |
| Q34194719 | How Bacteria Assemble Flagella |
| Q37125371 | Identification and characterization of a novel flagellum-dependent Salmonella-infecting bacteriophage, iEPS5 |
| Q55265058 | Insight into structural remodeling of the FlhA ring responsible for bacterial flagellar type III protein export. |
| Q89000706 | Insights into the evolution of bacterial flagellar motors from high-throughput in situ electron cryotomography and subtomogram averaging |
| Q42958279 | Interaction between FliJ and FlhA, components of the bacterial flagellar type III export apparatus |
| Q50126213 | Interaction of FliI, a component of the flagellar export apparatus, with flagellin and hook protein |
| Q28490035 | Interaction of the extreme N-terminal region of FliH with FlhA is required for efficient bacterial flagellar protein export |
| Q39887119 | Interactions of FliJ with the Salmonella type III flagellar export apparatus |
| Q39502769 | Intergenic suppression between the flagellar MS ring protein FliF of Salmonella and FlhA, a membrane component of its export apparatus |
| Q35161976 | Lateral flagellar gene system of Vibrio parahaemolyticus |
| Q40364421 | Mechanism of type-III protein secretion: Regulation of FlhA conformation by a functionally critical charged-residue cluster. |
| Q39610360 | Molecular characterization of a flagellar export locus of Helicobacter pylori. |
| Q50108067 | Molecular dissection of Salmonella FliH, a regulator of the ATPase FliI and the type III flagellar protein export pathway. |
| Q37232486 | Mutations in flk, flgG, flhA, and flhE that affect the flagellar type III secretion specificity switch in Salmonella enterica |
| Q39504100 | Mutations in genes involved in the flagellar export apparatus of the solvent-tolerant Pseudomonas putida DOT-T1E strain impair motility and lead to hypersensitivity to toluene shocks |
| Q50091919 | N-terminal signal region of FliK is dispensable for length control of the flagellar hook |
| Q38987844 | Not just an antibiotic target: Exploring the role of type I signal peptidase in bacterial virulence |
| Q47254500 | Novel insights into the mechanism of SepL-mediated control of effector secretion in enteropathogenic Escherichia coli. |
| Q30579291 | Randomly selected suppressor mutations in genes for NADH : quinone oxidoreductase-1, which rescue motility of a Salmonella ubiquinone-biosynthesis mutant strain |
| Q36363508 | Role of EscP (Orf16) in injectisome biogenesis and regulation of type III protein secretion in enteropathogenic Escherichia coli |
| Q28563581 | Role of the C-terminal cytoplasmic domain of FlhA in bacterial flagellar type III protein export |
| Q42462440 | 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. |
| Q33820597 | Secretion and assembly of regular surface structures in Gram-negative bacteria |
| Q28555062 | Structural and Functional Characterization of the Bacterial Type III Secretion Export Apparatus |
| Q39743825 | Substrate specificity classes and the recognition signal for Salmonella type III flagellar export |
| Q50103898 | Substrate specificity of type III flagellar protein export in Salmonella is controlled by subdomain interactions in FlhB. |
| Q39567045 | The flagellar switch genes fliM and fliN of Rhodobacter sphaeroides are contained in a large flagellar gene cluster |
| Q92824667 | The flexible linker of the secreted FliK ruler is required for export switching of the flagellar protein export apparatus |
| Q30611182 | The frequency and duration of Salmonella-macrophage adhesion events determines infection efficiency |
| Q48359452 | The role of intrinsically disordered C-terminal region of FliK in substrate specificity switching of the bacterial flagellar type III export apparatus. |
| Q42823992 | The target cell plasma membrane is a critical interface for Salmonella cell entry effector-host interplay |
| Q39110183 | The three-dimensional structure of the flagellar rotor from a clockwise-locked mutant of Salmonella enterica serovar Typhimurium |
| Q39566296 | Translation of the flagellar gene fliO of Salmonella typhimurium from putative tandem starts. |
| Q30850567 | Variability in bacterial flagella re-growth patterns after breakage |
| Q48015132 | hpaA mutants of Xanthomonas campestris pv. vesicatoria are affected in pathogenicity but retain the ability to induce host-specific hypersensitive reaction |
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