A novel mode of regulation of the Staphylococcus aureus catabolite control protein A (CcpA) mediated by Stk1 protein phosphorylation

Journal of Biological Chemistry

Volumn 287, Issue 52, 2012, Pages 43607-43619

  Leiba, Jade ^a   Hartmann, Torsten ^b   Cluzel, Marie Eve ^a   Cohen Gonsaud, Martin ^c   Delolme, Frédéric ^d   Bischoff, Markus ^b   Molle, Virginie ^a  

^a UNIVERSITÉ DE MONTPELLIER   (France)

^b SAARLAND UNIVERSITY   (Germany)

^c CENTRE DE BIOCHIMIE STRUCTURALE   (France)

^d UNIVERSITÉ LYON 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BACILLUS ANTHRACIS; BACILLUS SUBTILIS; BIOFILM FORMATION; CARBON CATABOLITE REPRESSION; CATABOLITE CONTROL PROTEIN A; CELL WALLS; DNA BINDING ACTIVITY; DNA BINDING DOMAIN; ELECTROPHORETIC MOBILITY SHIFT ASSAY; GRAM-POSITIVE PATHOGENS; IN-VITRO; MUTATIONAL ANALYSIS; NEGATIVE REGULATORS; PROTEIN KINASE; PROTEIN PHOSPHORYLATION; REGULATORY MECHANISM; S. AUREUS; STAPHYLOCOCCUS AUREUS; UP-REGULATION; WILD TYPES;

AMINO ACIDS; BACTERIA; DNA SEQUENCES; ELECTROPHORETIC MOBILITY; GENES; MASS SPECTROMETRY; PATHOGENS; PHOSPHORYLATION;

PROTEINS;

BACTERIAL PROTEIN; CATABOLITE CONTROL PROTEIN A; PROTEIN CITZ; PROTEIN HLA; PROTEIN SERINE THREONINE KINASE; PROTEIN STK1; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; BACILLUS ANTHRACIS; BACILLUS SUBTILIS; CONTROLLED STUDY; DNA BINDING; GEL MOBILITY SHIFT ASSAY; IN VITRO STUDY; IN VIVO STUDY; MASS SPECTROMETRY; MUTATIONAL ANALYSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; STAPHYLOCOCCUS AUREUS; STRUCTURE ANALYSIS; WILD TYPE;

AMINO ACID SUBSTITUTION; BACILLUS SUBTILIS; BACTERIAL PROTEINS; BIOFILMS; ESCHERICHIA COLI; GENE EXPRESSION REGULATION, BACTERIAL; MUTATION, MISSENSE; PHOSPHORYLATION; PROTEIN-SERINE-THREONINE KINASES; REPRESSOR PROTEINS; STAPHYLOCOCCUS AUREUS; TRANSCRIPTION, GENETIC; VIRULENCE FACTORS;

BACILLUS ANTHRACIS; BACILLUS SUBTILIS; POSIBACTERIA; STAPHYLOCOCCUS AUREUS;

EID: 84871547788     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.418913     Document Type: Article

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