Published in J Bacteriol on August 03, 2007
Motility and chemotaxis in alkaliphilic Bacillus species. Future Microbiol (2009) 1.31
Identical phosphatase mechanisms achieved through distinct modes of binding phosphoprotein substrate. Proc Natl Acad Sci U S A (2010) 1.11
Auxiliary phosphatases in two-component signal transduction. Curr Opin Microbiol (2010) 1.11
A bifunctional kinase-phosphatase in bacterial chemotaxis. Proc Natl Acad Sci U S A (2008) 1.00
The diverse CheC-type phosphatases: chemotaxis and beyond. Mol Microbiol (2008) 0.93
The HtrA protease of Borrelia burgdorferi degrades outer membrane protein BmpD and chemotaxis phosphatase CheX. Mol Microbiol (2013) 0.87
A remote CheZ orthologue retains phosphatase function. Mol Microbiol (2010) 0.87
Cellular stoichiometry of the chemotaxis proteins in Bacillus subtilis. J Bacteriol (2011) 0.86
Structure and activity of the flagellar rotor protein FliY: a member of the CheC phosphatase family. J Biol Chem (2013) 0.83
A selection that reports on protein-protein interactions within a thermophilic bacterium. Protein Eng Des Sel (2010) 0.79
Functional organization of a multimodular bacterial chemosensory apparatus. PLoS Genet (2014) 0.77
Two-component signal transduction. Annu Rev Biochem (2000) 19.12
A method for measuring chemotaxis and use of the method to determine optimum conditions for chemotaxis by Escherichia coli. J Gen Microbiol (1973) 18.10
Communication modules in bacterial signaling proteins. Annu Rev Genet (1992) 14.32
The two-component signaling pathway of bacterial chemotaxis: a molecular view of signal transduction by receptors, kinases, and adaptation enzymes. Annu Rev Cell Dev Biol (1997) 4.99
Adaptation kinetics in bacterial chemotaxis. J Bacteriol (1983) 4.31
Complete genome sequence of the alkaliphilic bacterium Bacillus halodurans and genomic sequence comparison with Bacillus subtilis. Nucleic Acids Res (2000) 4.11
Phosphorylation-dependent binding of a signal molecule to the flagellar switch of bacteria. Proc Natl Acad Sci U S A (1993) 3.89
Integration of multiple developmental signals in Bacillus subtilis through the Spo0A transcription factor. Genes Dev (1993) 3.76
Migration of bacteria in semisolid agar. Proc Natl Acad Sci U S A (1989) 3.70
Multiple protein-aspartate phosphatases provide a mechanism for the integration of diverse signals in the control of development in B. subtilis. Cell (1994) 3.22
Diversity in chemotaxis mechanisms among the bacteria and archaea. Microbiol Mol Biol Rev (2004) 3.15
How bacteria sense and swim. Annu Rev Microbiol (1995) 3.14
Structure and catalytic mechanism of the E. coli chemotaxis phosphatase CheZ. Nat Struct Biol (2002) 2.60
Simulated diffusion of phosphorylated CheY through the cytoplasm of Escherichia coli. J Bacteriol (2005) 2.29
CheZ phosphatase localizes to chemoreceptor patches via CheA-short. J Bacteriol (2003) 2.15
In vivo and in vitro chemotactic methylation in Bacillus subtilis. J Bacteriol (1981) 2.04
Single-cell FRET imaging of phosphatase activity in the Escherichia coli chemotaxis system. Proc Natl Acad Sci U S A (2004) 1.51
Distinct regions of bacterial flagellar switch protein FliM interact with FliG, FliN and CheY. J Mol Biol (1997) 1.51
Structure of FliM provides insight into assembly of the switch complex in the bacterial flagella motor. Proc Natl Acad Sci U S A (2006) 1.39
Bacillus subtilis CheC and FliY are members of a novel class of CheY-P-hydrolyzing proteins in the chemotactic signal transduction cascade. J Biol Chem (2004) 1.36
Chemotactic methylesterase promotes adaptation to high concentrations of attractant in Bacillus subtilis. J Biol Chem (1993) 1.33
A receptor-modifying deamidase in complex with a signaling phosphatase reveals reciprocal regulation. Cell (2006) 1.31
Structure and function of an unusual family of protein phosphatases: the bacterial chemotaxis proteins CheC and CheX. Mol Cell (2004) 1.28
Isolation and characterization of nonchemotactic CheZ mutants of Escherichia coli. J Bacteriol (2000) 1.26
CheX is a phosphorylated CheY phosphatase essential for Borrelia burgdorferi chemotaxis. J Bacteriol (2005) 1.23
Bacillus subtilis hydrolyzes CheY-P at the location of its action, the flagellar switch. J Biol Chem (2003) 1.23
Identification and characterization of FliY, a novel component of the Bacillus subtilis flagellar switch complex. Mol Microbiol (1992) 1.23
Protein phosphorylation and bacterial chemotaxis. Cold Spring Harb Symp Quant Biol (1988) 1.23
Bacillus subtilis CheN, a homolog of CheA, the central regulator of chemotaxis in Escherichia coli. J Bacteriol (1991) 1.20
Phosphorylation of the response regulator CheV is required for adaptation to attractants during Bacillus subtilis chemotaxis. J Biol Chem (2001) 1.19
Molecular characterization of a flagellar/chemotaxis operon in the spirochete Borrelia burgdorferi. FEMS Microbiol Lett (1997) 1.17
CheC and CheD interact to regulate methylation of Bacillus subtilis methyl-accepting chemotaxis proteins. Mol Microbiol (1996) 1.15
Chemotactic methylation and behavior in Bacillus subtilis: role of two unique proteins, CheC and CheD. Biochemistry (1995) 1.04
The role of heterologous receptors in McpB-mediated signalling in Bacillus subtilis chemotaxis. Mol Microbiol (2002) 1.04
Chemotactic methyltransferase promotes adaptation to repellents in Bacillus subtilis. J Biol Chem (1993) 1.03
Purification and characterization of Bacillus subtilis CheY. Biochemistry (1993) 1.00
CheY-dependent methylation of the asparagine receptor, McpB, during chemotaxis in Bacillus subtilis. J Biol Chem (1999) 0.91
Protein-protein interactions in the chemotaxis signalling pathway of Treponema denticola. Microbiology (2005) 0.87
Assays for CheC, FliY, and CheX as representatives of response regulator phosphatases. Methods Enzymol (2007) 0.84
Diversity in chemotaxis mechanisms among the bacteria and archaea. Microbiol Mol Biol Rev (2004) 3.15
Bacillus subtilis CheC and FliY are members of a novel class of CheY-P-hydrolyzing proteins in the chemotactic signal transduction cascade. J Biol Chem (2004) 1.36
A receptor-modifying deamidase in complex with a signaling phosphatase reveals reciprocal regulation. Cell (2006) 1.31
Large increases in attractant concentration disrupt the polar localization of bacterial chemoreceptors. Mol Microbiol (2005) 1.27
Bacillus subtilis hydrolyzes CheY-P at the location of its action, the flagellar switch. J Biol Chem (2003) 1.23
The three adaptation systems of Bacillus subtilis chemotaxis. Trends Microbiol (2008) 1.21
Bacillus subtilis CheD is a chemoreceptor modification enzyme required for chemotaxis. J Biol Chem (2002) 1.17
Aerotactic responses in bacteria to photoreleased oxygen. FEMS Microbiol Lett (2002) 1.04
The role of heterologous receptors in McpB-mediated signalling in Bacillus subtilis chemotaxis. Mol Microbiol (2002) 1.04
A PAS domain binds asparagine in the chemotaxis receptor McpB in Bacillus subtilis. J Biol Chem (2009) 1.02
The CheC phosphatase regulates chemotactic adaptation through CheD. J Biol Chem (2007) 0.97
The diverse CheC-type phosphatases: chemotaxis and beyond. Mol Microbiol (2008) 0.93
The Bacillus subtilis chemoreceptor McpC senses multiple ligands using two discrete mechanisms. J Biol Chem (2012) 0.90
The conserved cytoplasmic module of the transmembrane chemoreceptor McpC mediates carbohydrate chemotaxis in Bacillus subtilis. Mol Microbiol (2003) 0.88
The molecular basis of excitation and adaptation during chemotactic sensory transduction in bacteria. Contrib Microbiol (2009) 0.87
Effect of loss of CheC and other adaptational proteins on chemotactic behaviour in Bacillus subtilis. Microbiology (2004) 0.87
Ligand-induced conformational changes in the Bacillus subtilis chemoreceptor McpB determined by disulfide crosslinking in vivo. J Mol Biol (2004) 0.86
Cellular stoichiometry of the chemotaxis proteins in Bacillus subtilis. J Bacteriol (2011) 0.86
Attractant binding induces distinct structural changes to the polar and lateral signaling clusters in Bacillus subtilis chemotaxis. J Biol Chem (2010) 0.85
Transmembrane organization of the Bacillus subtilis chemoreceptor McpB deduced by cysteine disulfide crosslinking. J Mol Biol (2003) 0.85
Assays for CheC, FliY, and CheX as representatives of response regulator phosphatases. Methods Enzymol (2007) 0.84
Analysis of chimeric chemoreceptors in Bacillus subtilis reveals a role for CheD in the function of the McpC HAMP domain. J Bacteriol (2004) 0.84
The importance of the interaction of CheD with CheC and the chemoreceptors compared to its enzymatic activity during chemotaxis in Bacillus subtilis. PLoS One (2012) 0.83
Interactions among the three adaptation systems of Bacillus subtilis chemotaxis as revealed by an in vitro receptor-kinase assay. Mol Microbiol (2014) 0.81
Elucidation of the multiple roles of CheD in Bacillus subtilis chemotaxis. Mol Microbiol (2012) 0.80
Site-specific methylation in Bacillus subtilis chemotaxis: effect of covalent modifications to the chemotaxis receptor McpB. Microbiology (2010) 0.79
Receptor conformational changes enhance methylesterase activity during chemotaxis by Bacillus subtilis. Mol Microbiol (2004) 0.78