Matrix metalloproteinases (MMPs) have been implicated in the metastasis of tumors, and they are responsible for the breakdown of tissue surrounding the primary tumor site. Hence, inhibitors of MMPs offer a potential therapeutic benefit for diseases such as cancer and arthritis. We are using the techniques of molecular docking and database searching in identifying low nanomolar inhibitors of MMPs. In particular, we are focusing on the development of an accurate molecular mechanics force field to study metal ions representations in proteins. This knowledge will be coupled with determinations of the appropriate parameters in order to carry out the docking of different zinc-binding groups (hydroxamates, carboxylates, carboxyamines, etc). The results will be applied towards biologically interesting MMPs such as MT1-MMP or stromelysin-1.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001081-23
Application #
6347970
Study Section
Project Start
2000-07-01
Project End
2001-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
23
Fiscal Year
2000
Total Cost
$136
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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