Nitric oxide synthases (NOS) catalyze the 5-electron oxidation of L-Arg to nitric oxide (NO) and L-citruline. NO is a key molecular signal and neurotransmitter. Three different isozymes are present in the body- iNOS, eNOS, and bNOS. Many pathologies have been linked to either excessive or insufficient NO production. Thus, isozyme specific inhibitors are desirable from a medicinal point of view. The goal of this project is to determine structures of inhibitor bound complexes and to apply the structural information to the design of isozyme specific inhibitors.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119536
Study Section
Project Start
1999-03-01
Project End
2000-04-14
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
20
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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