Bacterial acyl-CoA mutase specifically catalyzes coenzyme B 12-dependent isomerization of 2-hydroxyisobutyryl-CoA and (S)-3-hydroxybutyryl-CoA

Journal of Biological Chemistry

Volumn 287, Issue 19, 2012, Pages 15502-15511

  Yaneva, Nadya ^a   Schuster, Judith ^a   Schäfer, Franziska ^a   Lede, Vera ^a   Przybylski, Denise ^a   Paproth, Torsten ^a   Harms, Hauke ^a   Müller, Roland H ^a   Rohwerder, Thore ^a  

^a HELMHOLTZ CENTRE FOR ENVIRONMENTAL RESEARCH UFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACID DEGRADATION; ACTIVE SITE; ACYL-COA; ACYL-COA SYNTHETASE; BACTERIAL STRAINS; CARBON SKELETON REARRANGEMENT; FUEL OXYGENATES; GENES ENCODING; INTERCONVERSIONS; KNOCKOUT MUTANT; METHYL TERT BUTYL ETHER; RADICAL ENZYMES; SEQUENCE ANALYSIS; SUBSTRATE SPECIFICITY; WILD-TYPE ENZYMES;

CARBOXYLIC ACIDS; CATALYSIS; DEGRADATION; ENZYMES; GENES;

SUBSTRATES;

2 HYDROXY 2 METHYLPROPIONIC ACID; 2 HYDROXYISOBUTYRYL COENZYME A; 2 HYDROXYISOBUTYRYL COENZYME A MUTASE; 3 HYDROXYBUTYRYL COENZYME A; BACTERIAL ENZYME; BUTYRIC ACID DERIVATIVE; CARBOXYLIC ACID; CHAPERONE; COBAMAMIDE; MUTASE; TERT BUTYL METHYL ETHER; UNCLASSIFIED DRUG;

AQUINCOLA TERTIARICARBONIS; ARTICLE; BACTERIAL STRAIN; BACTERIUM; BACTERIUM MUTANT; CATALYSIS; CHEMICAL STRUCTURE; DEGRADATION; ENZYME ACTIVITY; ENZYME SPECIFICITY; ENZYME SUBUNIT; GENE INACTIVATION; GENETIC ASSOCIATION; HYDROXYLATION; ISOMERIZATION; METABOLITE; NONHUMAN; PRIORITY JOURNAL; SEQUENCE ANALYSIS; WILD TYPE;

ACYL COENZYME A; AMINO ACID SEQUENCE; BACTERIAL PROTEINS; BETAPROTEOBACTERIA; BIOCATALYSIS; CATALYTIC DOMAIN; ELECTROPHORESIS, POLYACRYLAMIDE GEL; HYDROGEN-ION CONCENTRATION; HYDROXYBUTYRATES; INTRAMOLECULAR TRANSFERASES; ISOLEUCINE; ISOMERISM; KINETICS; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN SUBUNITS; SEQUENCE HOMOLOGY, AMINO ACID; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SUBSTRATE SPECIFICITY; VITAMIN B 12;

BACTERIA (MICROORGANISMS);

EID: 84860872187     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.314690     Document Type: Article

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