Targets of the cyclin-dependent kinase Cdk1

被引:0
作者
Jeffrey A. Ubersax
Erika L. Woodbury
Phuong N. Quang
Maria Paraz
Justin D. Blethrow
Kavita Shah
Kevan M. Shokat
David O. Morgan
机构
[1] University of California,Departments of Physiology and Biochemistry & Biophysics
[2] Biophysics,Department of Cellular and Molecular Pharmacology
[3] University of California,undefined
[4] University of California,undefined
[5] Genomics Institute of the Novartis Foundation,undefined
来源
Nature | 2003年 / 425卷
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摘要
The events of cell reproduction are governed by oscillations in the activities of cyclin-dependent kinases (Cdks)1. Cdks control the cell cycle by catalysing the transfer of phosphate from ATP to specific protein substrates. Despite their importance in cell-cycle control, few Cdk substrates have been identified2. Here, we screened a budding yeast proteomic library for proteins that are directly phosphorylated by Cdk1 in whole-cell extracts. We identified about 200 Cdk1 substrates, several of which are phosphorylated in vivo in a Cdk1-dependent manner. The identities of these substrates reveal that Cdk1 employs a global regulatory strategy involving phosphorylation of other regulatory molecules as well as phosphorylation of the molecular machines that drive cell-cycle events. Detailed analysis of these substrates is likely to yield important insights into cell-cycle regulation.
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页码:859 / 864
页数:5
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