A bacterial tyrosine aminomutase proceeds through retention or inversion of stereochemistry to catalyze its isomerization reaction

Journal of the American Chemical Society

Volumn 135, Issue 30, 2013, Pages 11193-11204

  Wanninayake, Udayanga ^a   Walker, Kevin D ^a,b  

^a MICHIGAN STATE UNIVERSITY   (United States)

^b Michigan State University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE STEREOCHEMISTRY; BIOLOGICALLY ACTIVE COMPOUNDS; INVERSION OF CONFIGURATION; ISOMERIZATION REACTION; LABELED SUBSTRATES; MEDICINAL CHEMISTRY; REACTION MECHANISM; TYROSINE ENANTIOMERS;

BIOACTIVITY; CATALYSIS; ISOMERIZATION; PROTONS; STEREOCHEMISTRY; STEREOSELECTIVITY;

AMINO ACIDS;

ACRYLIC ACID; BACTERIAL ENZYME; ETHOPROP; PROTON; SOLVENT; TYROSINE; TYROSINE AMINOMUTASE; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CATALYSIS; CATALYST; CHONDROMYCES CROCATUS; CONTROLLED STUDY; ELECTROSPRAY MASS SPECTROMETRY; ENANTIOSELECTIVITY; GAS; GAS CHROMATOGRAPHY; ION EXCHANGE; ISOMERIZATION; MYXOCOCCALES; NONHUMAN; PH; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEADY STATE; STEREOCHEMISTRY;

EID: 84881052336     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja403918w     Document Type: Article

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