This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.We propose to study a variety of proteins using synchrotron radiation. These include immunologically important molecules such as catalytic antibodies, anti-HIV antibodies, MHC/TCR complexes, NKG2D-receptor complexes, IL-2/receptor complexes, CD1, and CD3. We will also study the purine biosynthesis enzymes GAR transformylase and ATIC in complex with inhibitors. Finally, we will use the MAD technique to determine the structures for p115, a cell trafficking molecule and for CD14, the main lipopolysaccharide sensor on macrophages.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-29
Application #
7721729
Study Section
Special Emphasis Panel (ZRG1-BPC-E (40))
Project Start
2008-03-01
Project End
2009-02-28
Budget Start
2008-03-01
Budget End
2009-02-28
Support Year
29
Fiscal Year
2008
Total Cost
$2,660
Indirect Cost
Name
Stanford University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
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