Rapid progress in the functional characterization of proteins involved in signal transduction and cell cycle regulation has highlighted their importance for appropriate signal responses and regulation of cell differentiation, cell growth and cell division. We are working on the crystal structure of a complex of cyclin dependent kinase 2 with cyclin A. CDKs are central to cell cycle regulation and can only be activated after complex formation with a cyclin. Hence a complex structure will provide important structural information about the activation process of CDK2.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR001209-23S1
Application #
6658521
Study Section
Project Start
2002-03-01
Project End
2003-02-28
Budget Start
Budget End
Support Year
23
Fiscal Year
2002
Total Cost
$143,176
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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