Protein kinase inhibition by staurosporine revealed in details of the molecular interaction with CDK2

Nature Structural Biology

Volumn 4, Issue 10, 1997, Pages 796-801

[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

CDK2 PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE; CYCLIN DEPENDENT KINASE 2; ENZYME INHIBITOR; PROTEIN KINASE; PROTEIN SERINE THREONINE KINASE; RECOMBINANT PROTEIN; STAUROSPORINE;

AMINO ACID SEQUENCE; ANIMAL; ARMYWORM; BINDING SITE; BIOSYNTHESIS; CHEMICAL STRUCTURE; CHEMISTRY; COMPARATIVE STUDY; CONFORMATION; DRUG ANTAGONISM; GENETIC TRANSFECTION; HUMAN; LETTER; MOLECULAR GENETICS; PROTEIN CONFORMATION; PROTEIN SECONDARY STRUCTURE; REPRODUCIBILITY; SEQUENCE ALIGNMENT; X RAY CRYSTALLOGRAPHY;

AMINO ACID SEQUENCE; ANIMALS; BINDING SITES; CDC2-CDC28 KINASES; CRYSTALLOGRAPHY, X-RAY; CYCLIN-DEPENDENT KINASE 2; CYCLIN-DEPENDENT KINASES; ENZYME INHIBITORS; HUMANS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR SEQUENCE DATA; PROTEIN CONFORMATION; PROTEIN KINASES; PROTEIN STRUCTURE, SECONDARY; PROTEIN-SERINE-THREONINE KINASES; RECOMBINANT PROTEINS; REPRODUCIBILITY OF RESULTS; SEQUENCE ALIGNMENT; SPODOPTERA; STAUROSPORINE; TRANSFECTION;

EID: 0031253655     PISSN: 10728368     EISSN: None     Source Type: Journal    
DOI: 10.1038/nsb1097-796     Document Type: Article

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