We propose to examine by Cu and Fe EXAFS the cytochrome bo quinol oxidase of E. coli as an analog of the mammalian cytochrome c oxidase (aa3). Cytochrome bo has been cloned and expressed and site-directed mutated proteins have been characterized. Since cytochrome bo is one member of the cytochrome oxidase superfamily that does not contain the CuA site, Cu EXAFS will be able to directly probe the CuB coordination environment without interference from the other Cu site. We will take advantage of this characteristic to explore the structure of the dinuclear heme o-CuB site in various redox states, and in the presence of substrate O2, competitive inhibitors, and exogenous ligands.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR001209-23S1
Application #
6658654
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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