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FlgM Is Secreted by the Flagellar Export Apparatus in Bacillus subtilis

https://doi.org/10.1128/jb.02324-14
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Multiple active forms of a novel serine protease from Bacillus subtilis
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Excretion of the anti-sigma factor through a flagellar substructure couples flagellar gene expression with flagellar assembly in Salmonella typhimurium
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The Type III Flagellar Export Specificity Switch is Dependent on FliK Ruler and a Molecular Clock
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Cloning, genetic organization, and characterization of a structural gene encoding bacillopeptidase F from Bacillus subtilis.
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Eubacterial sigma-factors
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Crystal Structure of the Flagellar σ/Anti-σ Complex σ28/FlgM Reveals an Intact σ Factor in an Inactive Conformation
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RodZ (YfgA) is required for proper assembly of the MreB actin cytoskeleton and cell shape in E. coli
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An infrequent molecular ruler controls flagellar hook length in Salmonella enterica
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Coordinating assembly of a bacterial macromolecular machine
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Completion of the hook–basal body complex of the Salmonella typhimurium flagellum is coupled to FlgM secretion and fliC transcription
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Overproduction and Characterization of the Bacillus subtilis Anti-sigma Factor FlgM
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The wprA gene of Bacillus subtilis 168, expressed during exponential growth, encodes a cell-wall-associated protease
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Cell population heterogeneity during growth of Bacillus subtilis
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A novel transcriptional regulation mechanism in the flagellar regulon of Salmonella typhimurium : an anti‐sigma factor inhibits the activity of the flagellum‐specific Sigma factor, σ F
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CsrA of Bacillus subtilis regulates translation initiation of the gene encoding the flagellin protein ( hag ) by blocking ribosome binding
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MinJ (YvjD) is a topological determinant of cell division in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06871.xopenalex-snapshot
Interaction of FliK with the bacterial flagellar hook is required for efficient export specificity switching
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07112.xopenalex-snapshot
Gene position in a long operon governs motility development in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07755.xopenalex-snapshot
DegU‐phosphate activates expression of the anti‐sigma factor FlgM in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07822.xopenalex-snapshot
CsrA-FliW interaction governs flagellin homeostasis and a checkpoint on flagellar morphogenesis in Bacillus subtilis
inferredcites →https://doi.org/10.1126/science.1079914openalex-snapshot
RacA, a Bacterial Protein That Anchors Chromosomes to the Cell Poles
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Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator
inferredcites →https://doi.org/10.1128/jb.00018-09openalex-snapshot
The Helicobacter pylori Anti-Sigma Factor FlgM Is Predominantly Cytoplasmic and Cooperates with the Flagellar Basal Body Protein FlhA
inferredcites →https://doi.org/10.1128/jb.00444-12openalex-snapshot
Molecular Characterization of the Flagellar Hook in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.00521-09openalex-snapshot
Role of the σ D -Dependent Autolysins in Bacillus subtilis Population Heterogeneity
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Replacement of the Bacillus subtilis subtilisin structural gene with an In vitro-derived deletion mutation
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Cloning of the neutral protease gene of Bacillus subtilis and the use of the cloned gene to create an in vitro-derived deletion mutation
inferredcites →https://doi.org/10.1128/jb.170.4.1568-1574.1988openalex-snapshot
Cloning, sequencing, and disruption of the Bacillus subtilis sigma 28 gene
inferredcites →https://doi.org/10.1128/jb.171.6.3095-3101.1989openalex-snapshot
The Bacillus subtilis flagellin gene (hag) is transcribed by the sigma 28 form of RNA polymerase
inferredcites →https://doi.org/10.1128/jb.172.2.1019-1023.1990openalex-snapshot
Isolation and characterization of a novel extracellular metalloprotease from Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.172.6.3435-3443.1990openalex-snapshot
Studies of sigma D-dependent functions in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.173.11.3573-3579.1991openalex-snapshot
The flaA locus of Bacillus subtilis is part of a large operon coding for flagellar structures, motility functions, and an ATPase-like polypeptide
inferredcites →https://doi.org/10.1128/jb.173.21.6889-6895.1991openalex-snapshot
Cloning and characterization of the gene for an additional extracellular serine protease of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.173.7.2301-2310.1991openalex-snapshot
Negative regulatory loci coupling flagellin synthesis to flagellar assembly in Salmonella typhimurium
inferredcites →https://doi.org/10.1128/jb.174.13.4197-4204.1992openalex-snapshot
An operon of Bacillus subtilis motility genes transcribed by the sigma D form of RNA polymerase
inferredcites →https://doi.org/10.1128/jb.175.3.795-801.1993openalex-snapshot
High-level transcription of the major Bacillus subtilis autolysin operon depends on expression of the sigma D gene and is affected by a sin (flaD) mutation
inferredcites →https://doi.org/10.1128/jb.176.15.4492-4500.1994openalex-snapshot
Identification of flagellar synthesis regulatory and structural genes in a sigma D-dependent operon of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.176.8.2427-2434.1994openalex-snapshot
Characterization of the sigD transcription unit of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.178.11.3113-3118.1996openalex-snapshot
Role of FlgM in sigma D-dependent gene expression in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.180.14.3548-3555.1998openalex-snapshot
Dual Promoters Are Responsible for Transcription Initiation of the fla/che Operon in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.182.17.4841-4848.2000openalex-snapshot
Relative Roles of the fla/che P A , P D-3 , and P sigD Promoters in Regulating Motility and sigD Expression in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.184.2.596-599.2002openalex-snapshot
epr Is Transcribed from a ς D Promoter and Is Involved in Swarming of Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.185.22.6666-6677.2003openalex-snapshot
Localization of the Vegetative Cell Wall Hydrolases LytC, LytE, and LytF on the Bacillus subtilis Cell Surface and Stability of These Enzymes to Cell Wall-Bound or Extracellular Proteases
inferredcites →https://doi.org/10.1128/jvi.14.6.1343-1348.1974openalex-snapshot
Transduction in Bacillus subtilis by Bacteriophage SPP1
inferredcites →https://doi.org/10.1128/mmbr.59.1.1-30.1995openalex-snapshot
The sigma factors of Bacillus subtilis
inferredcites →https://doi.org/10.1128/mmbr.64.4.694-708.2000openalex-snapshot
Coupling of Flagellar Gene Expression to Flagellar Assembly in Salmonella enterica Serovar Typhimurium and Escherichia coli
inferredcites →https://doi.org/10.1146/annurev.ge.26.120192.001023openalex-snapshot
GENETICS AND BIOGENESIS OF BACTERIAL FLAGELLA
inferredcites →https://doi.org/10.1146/annurev.micro.52.1.231openalex-snapshot
THE ANTI-SIGMA FACTORS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Inefficient Secretion of Anti-Sigma Factor FlgM Inhibits Bacterial Motility at High Temperature
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Motility, Chemotaxis and Aerotaxis Contribute to Competitiveness during Bacterial Pellicle Biofilm Development
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The SinR·SlrR Heteromer Attenuates Transcription of a Long Operon of Flagellar Genes in Bacillus subtilis
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c-di-GMP Arms an Anti-σ to Control Progression of Multicellular Differentiation in Streptomyces
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FliS/flagellin/FliW heterotrimer couples type III secretion and flagellin homeostasis
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Flagellar rotation facilitates the transfer of a bacterial conjugative plasmid
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Flagellar toxicity: Flagellar synthesis is lytic for Bacillus subtilis in the absence of PBP1
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Translation Control of Swarming Proficiency in Bacillus subtilis by 5-Amino-pentanolylated Elongation Factor P
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Greedy reduction ofBacillus subtilisgenome yields emergent phenotypes of high resistance to a DNA damaging agent and low evolvability
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Bacterial surface motility is modulated by colony-scale flow and granular jamming
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A conjugative plasmid exploits flagella rotation as a cue to facilitate its transfer
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Physical factors contributing to regulation of bacterial surface motility
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Noncontact Cohesive Swimming of Bacteria in Two-Dimensional Liquid Films
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Impaired competence in flagellar mutants of Bacillus subtilis is connected to the regulatory network governed by DegU
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Analysis of a flagellar filament cap mutant reveals that HtrA serine protease degrades unfolded flagellin protein in the periplasm of Borrelia burgdorferi
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Motility control through an anti‐activation mechanism in Agrobacterium tumefaciens
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Flagellar motor remodeling during swarming requires FliL
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TasA Fibre Interactions Are Necessary for Bacillus subtilis Biofilm Structure
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Surface Sensing for Paenibacillus sp. NAIST15-1 Flagellar Gene Expression on Solid Medium
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Unchaining mini Bacillus Strain PG10: Relief of FlgM-Mediated Repression of Autolysin Genes
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Surveying a Swarm: Experimental Techniques To Establish and Examine Bacterial Collective Motion
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Tn FLX : a Third-Generation mariner -Based Transposon System for Bacillus subtilis
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Functional Analysis of the Alternative Sigma-28 Factor FliA and Its Anti-Sigma Factor FlgM of the Nonflagellated Legionella Species L. oakridgensis
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CwlQ Is Required for Swarming Motility but Not Flagellar Assembly in Bacillus subtilis
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Identification of Genes Required for Swarming Motility in Bacillus subtilis Using Transposon Mutagenesis and High-Throughput Sequencing (TnSeq)
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Molecular and Cell Biological Analysis of SwrB in Bacillus subtilis
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CodY Regulates SigD Levels and Activity by Binding to Three Sites in the fla / che Operon
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Spx inhibits expression of the SwrA•DegU master flagellar activator in Bacillus subtilis
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Assembly Order of Flagellar Rod Subunits in Bacillus subtilis
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SwrD (YlzI) Promotes Swarming in Bacillus subtilis by Increasing Power to Flagellar Motors
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FliL Functions in Diverse Microbes to Negatively Modulate Motor Output via Its N-Terminal Region
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Robust Stoichiometry of FliW-CsrA Governs Flagellin Homeostasis and Cytoplasmic Organization in Bacillus subtilis
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Active removal of inhibitory components drives the flagellar type 3 secretion-specificity switch
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Small amounts of misassembly can have disproportionate effects on pangenome-based metagenomic analyses
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Regulatory divergence and functional diversification of a c-di-GMP-controlled sigma factor in Actinomycetota
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Functional Regulators of Bacterial Flagella
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Flagella disruption in Bacillus subtilis increases amylase production yield
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Functional Activation of the Flagellar Type III Secretion Export Apparatus
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Bacillus subtilis Bactofilins Are Essential for Flagellar Hook- and Filament Assembly and Dynamically Localize into Structures of Less than 100 nm Diameter underneath the Cell Membrane
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Flagellar Basal Body Structural Proteins FlhB, FliM, and FliY Are Required for Flagellar-Associated Protein Expression in Listeria monocytogenes
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Switching and Torque Generation in Swarming E. coli
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The fliK Gene Is Required for the Resistance of Bacillus thuringiensis to Antimicrobial Peptides and Virulence in Drosophila melanogaster
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Proteolytic Surface-Shaving and Serotype-Dependent Expression of SPI-1 Invasion Proteins in Salmonella enterica Subspecies enterica
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High-Throughput Analysis of the Flagella FliK-Dependent Surfaceome and Secretome in Bacillus thuringiensis
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Bacterial Flagellar Filament: A Supramolecular Multifunctional Nanostructure
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Faculty Opinions recommendation of Bacterial nanotubes as a manifestation of cell death.
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Additional file 1 of Flagella disruption in Bacillus subtilis increases amylase production yield
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Additional file 3 of Flagella disruption in Bacillus subtilis increases amylase production yield
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