Substrate-protein interaction in human tryptophan dioxygenase: The critical role of H76

Journal of the American Chemical Society

Volumn 131, Issue 9, 2009, Pages 3260-3270

  Batabyal, Dipanwita ^a   Yeh, Syun Ru ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM COMPOUNDS; CARBOXYLATION; ELECTRONIC PROPERTIES; HYDROPHOBICITY; OXIDATION;

ACTIVE SITE; ACTIVITY ASSAYS; BASE CATALYST; DIOXYGENASES; ELECTRONIC CONFIGURATION; H-BONDING; HEME-PROTEINS; HYDROPHOBIC INTERACTIONS; NH GROUPS; OXIDATION REACTIONS; PROTEIN INTERACTION; PROTEIN MATRICES; RATE-LIMITING STEPS; RESONANCE RAMAN; SPECIFIC INTERACTION; TERNARY COMPLEX;

AMINO ACIDS;

TRYPTOPHAN; TRYPTOPHAN 2,3 DIOXYGENASE; CARBOXYLIC ACID; INDOLE DERIVATIVE; QUATERNARY AMMONIUM DERIVATIVE;

ARTICLE; COMPLEX FORMATION; ENZYME ACTIVITY; ENZYME BINDING; ENZYME SUBSTRATE; GENE MUTATION; HYDROGEN BOND; PROTEIN INTERACTION; BIOCATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; ENZYME ACTIVE SITE; GENETICS; HUMAN; METABOLISM; MUTATION; OXIDATION REDUCTION REACTION;

BIOCATALYSIS; CARBOXYLIC ACIDS; CATALYTIC DOMAIN; HUMANS; HYDROGEN BONDING; INDOLES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; MUTATION; OXIDATION-REDUCTION; QUATERNARY AMMONIUM COMPOUNDS; TRYPTOPHAN OXYGENASE;

EID: 70350494610     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja807969a     Document Type: Article

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