Cellular processes such as vessicle transport and chromosome segregation depend on motor proteins like kinesin to actively create force and movement along microtubules. Many disease processes, in turn, might be altered by a small molecule inhibitor of kinesin's ATP-driven movement. To discover such an inhibitor we are using DOCK4.0 to search through a database of compounds that may bind to sites on kinesin and inhibit movement allosterically. The structure of kinesin will be viewed with the resources of the Computer Graphics Laboratory along with the results of computations aimed at identifying binding sites and the docking of potential ligands. The interactive graphics and computational software will aid our search for potential inhibitors.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001081-21
Application #
6280265
Study Section
Project Start
1998-07-01
Project End
1999-06-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
21
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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