The localization of human cyclins B1 and B2 determines CDK1 substrate specificity and neither enzyme requires MEK to disassemble the Golgi apparatus

Journal of Cell Biology

Volumn 152, Issue 5, 2001, Pages 945-958

  Draviam, Viji Mythily ^a   Orrechia, Simona ^b   Lowe, Martin ^c   Pardi, Ruggero ^b   Pines, Jonathon ^a,d  

^a IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^b VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^c UNIVERSITY OF MANCHESTER   (United Kingdom)

^d UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

CDK; Cyclin; Golgi apparatus; Mitosis; Protein kinase

Indexed keywords

CYCLIN B1; CYCLIN B2; CYCLIN DEPENDENT KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE KINASE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CHROMOSOME CONDENSATION; ENZYME ACTIVITY; ENZYME SPECIFICITY; GOLGI COMPLEX; HUMAN; HUMAN CELL; MICROTUBULE; MITOSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN LOCALIZATION;

ANIMALS; CDC2 PROTEIN KINASE; CHO CELLS; CHROMOSOMES; CRICETINAE; CYCLIN B; CYTOSKELETON; G0 PHASE; G1 PHASE; GOLGI APPARATUS; HELA CELLS; HUMANS; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MITOSIS; PROTEIN KINASES; PROTEIN TRANSPORT; RECOMBINANT FUSION PROTEINS; SUBSTRATE SPECIFICITY;

ANIMALIA;

EID: 0035809921     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.152.5.945     Document Type: Article

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