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Volumn 39, Issue 41, 2000, Pages 12534-12542
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Preparation, characterization, and the crystal structure of the inhibitor ZK-807834 (CI-1031) complexed with factor Xa
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Author keywords
[No Author keywords available]
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Indexed keywords
BLOOD CLOTTING FACTOR 10A;
BLOOD CLOTTING FACTOR 10A INHIBITOR;
N [2 (5 AMIDINO 2 HYDROXYPHENOXY) 3,5 DIFLUORO 6 [3 (1 METHYL 1H 2 IMIDAZOLIN 2 YL)PHENOXY] 4 PYRIDINYL] N METHYLGLYCINE;
N [2 [5 [AMINO(IMINO)METHYL] 2 HYDROXYPHENOXY] 3,5 DIFLUORO 6 [3 (4,5 DIHYDRO 1 METHYL 1H IMIDAZOL 2 YL)PHENOXY]PYRIDIN 4 YL] N METHYLGLYCINE;
SERINE PROTEINASE;
SERINE PROTEINASE INHIBITOR;
TRYPSIN;
UNCLASSIFIED DRUG;
ARTICLE;
BLOOD CLOTTING;
CAPILLARY ELECTROPHORESIS;
COMPLEX FORMATION;
CRYSTAL STRUCTURE;
HUMAN;
HYDROGEN BOND;
MASS SPECTROMETRY;
MOLECULAR INTERACTION;
PRIORITY JOURNAL;
PROTEIN PURIFICATION;
SYNTHESIS;
1-CARBOXYGLUTAMIC ACID;
AMIDINES;
AMINO ACID SEQUENCE;
ANIMALS;
BINDING, COMPETITIVE;
CATTLE;
COMPUTER SIMULATION;
CRYSTALLIZATION;
CRYSTALLOGRAPHY, X-RAY;
FACTOR XA;
HUMANS;
MACROMOLECULAR SUBSTANCES;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
PYRIDINES;
SERINE PROTEINASE INHIBITORS;
STEREOISOMERISM;
TRYPSIN;
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EID: 0034680369
PISSN: 00062960
EISSN: None
Source Type: Journal
DOI: 10.1021/bi001477q Document Type: Article |
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Times cited : (111)
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References (25)
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