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Volumn 277, Issue 31, 2002, Pages 28080-28087
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Crystal structures of inhibitor complexes reveal an alternate binding mode in orotidine-5′-monophosphate decarboxylase
a,b
a,b,c
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEXATION;
CRYSTAL STRUCTURE;
ENZYMES;
LIGANDS;
BIOCHEMISTRY;
6 HYDROXYURIDINE 5' PHOSPHATE;
ALANINE;
ARGININE;
BARBITURIC ACID DERIVATIVE;
BARBITURIC ACID RIBOSYL 5' PHOSPHATE;
GLYCINE;
OROTIDINE 5' PHOSPHATE DECARBOXYLASE;
PHOSPHATE;
UNCLASSIFIED DRUG;
URIDINE DERIVATIVE;
XANTHINE DERIVATIVE;
XANTHOSINE 5 PHOSPHATE;
AMINO ACID SUBSTITUTION;
ARTICLE;
CRYSTAL STRUCTURE;
ENZYME INHIBITOR INTERACTION;
ENZYME STRUCTURE;
GENE MUTATION;
INHIBITION KINETICS;
LIGAND BINDING;
METHANOBACTERIUM THERMOAUTOTROPHICUM;
NONHUMAN;
PHOSPHATE METABOLISM;
PRIORITY JOURNAL;
PROTEIN LOCALIZATION;
PROTEIN STRUCTURE;
AMINO ACID SUBSTITUTION;
BINDING SITES;
CRYSTALLOGRAPHY, X-RAY;
ENZYME INHIBITORS;
METHANOBACTERIUM;
MODELS, MOLECULAR;
MUTAGENESIS, SITE-DIRECTED;
OROTIDINE-5'-PHOSPHATE DECARBOXYLASE;
PROTEIN CONFORMATION;
RECOMBINANT PROTEINS;
BACTERIA (MICROORGANISMS);
METHANOBACTERIUM;
METHANOTHERMOBACTER THERMAUTOTROPHICUS;
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EID: 0037008729
PISSN: 00219258
EISSN: None
Source Type: Journal
DOI: 10.1074/jbc.M202362200 Document Type: Article |
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Times cited : (34)
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References (27)
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