scholarly article | Q13442814 |
P2093 | author name string | Tohru Minamino | |
Keiichi Namba | |||
Takanori Hirano | |||
Robert M Macnab | |||
P2860 | cites work | Functional insights from the structure of the 30S ribosomal subunit and its interactions with antibiotics | Q27627265 |
Identification of the YopE and YopH domains required for secretion and internalization into the cytosol of macrophages, using the cyaA gene fusion approach | Q33638561 | ||
Export of an N-terminal fragment of Escherichia coli flagellin by a flagellum-specific pathway | Q34285883 | ||
Flagellar assembly in Salmonella typhimurium: analysis with temperature-sensitive mutants | Q36159115 | ||
Incomplete flagellar structures in Escherichia coli mutants | Q36322064 | ||
Examination of bacterial flagellation by dark-field microscopy | Q37348026 | ||
Quick transformation in Salmonella typhimurium LT2. | Q37912600 | ||
Components of the Salmonella flagellar export apparatus and classification of export substrates | Q39494402 | ||
Interaction between FliE and FlgB, a proximal rod component of the flagellar basal body of Salmonella | Q39499639 | ||
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 | ||
Mutations in fliK and flhB affecting flagellar hook and filament assembly in Salmonella typhimurium | Q39841418 | ||
The FliO, FliP, FliQ, and FliR proteins of Salmonella typhimurium: putative components for flagellar assembly | Q39847377 | ||
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 | ||
Excretion of unassembled flagellin by Salmonella typhimurium mutants deficient in hook-associated proteins. | Q39969532 | ||
Incomplete flagellar structures in nonflagellate mutants of Salmonella typhimurium | Q39989881 | ||
FlgB, FlgC, FlgF and FlgG. A family of structurally related proteins in the flagellar basal body of Salmonella typhimurium | Q41196112 | ||
Ribosomal RNA and protein mutants resistant to spectinomycin | Q41204307 | ||
A mRNA signal for the type III secretion of Yop proteins by Yersinia enterocolitica | Q41487461 | ||
Substrate complexes and domain organization of the Salmonella flagellar export chaperones FlgN and FliT. | Q42136963 | ||
Flagellin polymerisation control by a cytosolic export chaperone. | Q42425518 | ||
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 | ||
The type III secretion determinants of the flagellar anti-transcription factor, FlgM, extend from the amino-terminus into the anti-sigma28 domain | Q42467848 | ||
Flagellar hook and hook-associated proteins of Salmonella typhimurium and their relationship to other axial components of the flagellum | Q42481365 | ||
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 | ||
The role in flagellar rod assembly of the N-terminal domain of Salmonella FlgJ, a flagellum-specific muramidase | Q42510064 | ||
Substrate-specific binding of hook-associated proteins by FlgN and FliT, putative chaperones for flagellum assembly | Q48565780 | ||
Molecular dissection of Salmonella FliH, a regulator of the ATPase FliI and the type III flagellar protein export pathway. | Q50108067 | ||
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 | ||
Substrate specificity switching of the flagellum-specific export apparatus during flagellar morphogenesis in Salmonella typhimurium | Q50124742 | ||
Interaction of FliI, a component of the flagellar export apparatus, with flagellin and hook protein | Q50126213 | ||
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 | ||
Genetic Analysis of H2, the Structural Gene for Phase-2 Flagellin in Salmonella | Q50209142 | ||
Translation/Secretion Coupling by Type III Secretion Systems | Q59210021 | ||
Spa15 of Shigella flexneri, a third type of chaperone in the type III secretion pathway | Q77937556 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2485-2492 | |
P577 | publication date | 2003-04-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Substrate specificity classes and the recognition signal for Salmonella type III flagellar export | |
P478 | volume | 185 |
Q47614276 | A Naturally Occurring Deletion in FliE from Salmonella enterica Serovar Dublin Results in an Aflagellate Phenotype and Defective Proinflammatory Properties |
Q41950585 | A regulatory checkpoint during flagellar biogenesis in Campylobacter jejuni initiates signal transduction to activate transcription of flagellar genes. |
Q33617090 | Application of a short, disordered N-terminal flagellin segment, a fully functional flagellar type III export signal, to expression of secreted proteins. |
Q40315435 | Biochemical Characterization of the Flagellar Rod Components of Rhodobacter sphaeroides: Properties and Interactions. |
Q37360959 | Comparative analysis of the secretion capability of early and late flagellar type III secretion substrates. |
Q46793605 | Distinct roles of the FliI ATPase and proton motive force in bacterial flagellar protein export |
Q61446498 | Engineering the flagellar type III secretion system: improving capacity for secretion of recombinant protein |
Q38257520 | Extracellular secretion of a recombinant therapeutic peptide by Bacillus halodurans utilizing a modified flagellin type III secretion system |
Q48144320 | Extracellular secretion of polypeptides using a modified Escherichia coli flagellar secretion apparatus |
Q36318616 | Flk prevents premature secretion of the anti-sigma factor FlgM into the periplasm |
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 |
Q42187679 | Functional Activation of the Flagellar Type III Secretion Export Apparatus |
Q34286388 | High-throughput comparison of gene fitness among related bacteria |
Q34194719 | How Bacteria Assemble Flagella |
Q42321006 | Identification of a putative glycosyltransferase responsible for the transfer of pseudaminic acid onto the polar flagellin of Aeromonas caviae Sch3N. |
Q34513676 | Identification of new flagellar genes of Salmonella enterica serovar Typhimurium |
Q92661378 | In Vitro Autonomous Construction of the Flagellar Axial Structure in Inverted Membrane Vesicles |
Q55385008 | In Vitro Reconstitution of Functional Type III Protein Export and Insights into Flagellar Assembly. |
Q27677937 | Inhibition of a type III secretion system by the deletion of a short loop in one of its membrane proteins |
Q28490083 | Interaction of FliK with the bacterial flagellar hook is required for efficient export specificity switching |
Q50004876 | Interactions of bacterial flagellar chaperone-substrate complexes with FlhA contribute to co-ordinating assembly of the flagellar filament |
Q41821295 | MotD of Sinorhizobium meliloti and related alpha-proteobacteria is the flagellar-hook-length regulator and therefore reassigned as FliK. |
Q37232486 | Mutations in flk, flgG, flhA, and flhE that affect the flagellar type III secretion specificity switch in Salmonella enterica |
Q48146965 | Novel insights into the mechanism of well-ordered assembly of bacterial flagellar proteins in Salmonella. |
Q34564953 | Posttranscriptional control of the Salmonella enterica flagellar hook protein FlgE |
Q64273852 | Robust Stoichiometry of FliW-CsrA Governs Flagellin Homeostasis and Cytoplasmic Organization in Bacillus subtilis |
Q39521719 | Role of the Dc domain of the bacterial hook protein FlgE in hook assembly and function. |
Q41457272 | Secretion of YscP from Yersinia enterocolitica is essential to control the length of the injectisome needle but not to change the type III secretion substrate specificity |
Q40387779 | Secretome analysis of diarrhea-inducing strains of Escherichia coli |
Q35788077 | Self-assembly and type III protein export of the bacterial flagellum |
Q42246455 | Sorting of early and late flagellar subunits after docking at the membrane ATPase of the type III export pathway |
Q30846664 | Straight and rigid flagellar hook made by insertion of the FlgG specific sequence into FlgE. |
Q35586143 | Substrate recognition by the Yersinia type III protein secretion machinery |
Q93013426 | Suppressor mutations in ribosomal proteins and FliY restore Bacillus subtilis swarming motility in the absence of EF-P |
Q28252092 | The bacterial flagellar motor: structure and function of a complex molecular machine |
Q35985882 | The mechanism of outer membrane penetration by the eubacterial flagellum and implications for spirochete evolution |
Q35051271 | Theoretical and computational investigation of flagellin translocation and bacterial flagellum growth |
Q39787232 | Use of a Novel Report Protein to Study the Secretion Signal of Flagellin in Bacillus subtilis. |
Q42420020 | Weak Interactions between Salmonella enterica FlhB and Other Flagellar Export Apparatus Proteins Govern Type III Secretion Dynamics |
Q39797612 | Xenocin export by the flagellar type III pathway in Xenorhabdus nematophila |
Q40936347 | Yersinia enterocolitica type III secretion depends on the proton motive force but not on the flagellar motor components MotA and MotB |
Search more.