A nonproteolytic function of the proteasome is required for the dissociation of CDc2 and cyclin B at the end of M phase

Genes and Development

Volumn 14, Issue 18, 2000, Pages 2344-2357

  Nishiyama, Atsuya ^a   Tachibana, Kazunori ^a   Igarashi, Yuko ^b   Yasuda, Hideyo ^b   Tanahashi, Nobuyuki ^c   Tanaka, Keiji ^c,d   Ohsumi, Keita ^a   Kishimoto, Takeo ^a,d  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

^c TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Cell cycle; Cyclin B Cdc2; Proteasome; Protein unfolding; Xenopus egg extracts

Indexed keywords

CYCLIN B; PROTEASOME; PROTEASOME 20S; PROTEASOME 26S; PROTEIN KINASE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISSOCIATION; EGG; ENZYME ACTIVITY; ENZYME INACTIVATION; ENZYME REGULATION; ENZYME SUBUNIT; MITOSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN STABILITY; XENOPUS;

ANIMALS; CDC2 PROTEIN KINASE; CYCLIN B; CYSTEINE ENDOPEPTIDASES; MITOSIS; MULTIENZYME COMPLEXES; OVUM; PEPTIDE HYDROLASES; PRECIPITIN TESTS; PROTAMINE KINASE; PROTEASOME ENDOPEPTIDASE COMPLEX; UBIQUITINS; XENOPUS;

EID: 0034665742     PISSN: 08909369     EISSN: None     Source Type: Journal    
DOI: 10.1101/gad.823200     Document Type: Article

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