Superoxide dismutases are essential for aerobic life. Iron- and manganese-dependent enzymes share a common protein structure, however they exhibit metal-ion specificity linked to the extended protein environment. Several residues, including Q143 and H30, are important in making indirect interactions with the active-site metal of the human manganese dependent enzyme. High resolution structures of the Q143R, Q143A, H30Q, and H30V mutants, not attainable at our in-house source, will give insight into the physical interactions that tune the redox potential of the enzyme and confer metal-ion specificity on the enzyme.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119552
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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