To understand the molecular basis of signal transduction through TRAF2, we propose to collect MAD data to determine the crystal structure of the C-terminal portion of TRAF2. TRAF proteins associate with and transduce signals from TNF receptor superfamily members to regulate various inflammatory and immune responses. To date, no detailed structural information has been obtained for this class of proteins. We expect our crystal structure to reveal how TRAFs oligomerize, and how oligomerization plays a role in receptor specificity. We have successfully grown crystals of the C-terminal TRAF domain of TRAF2. The crystals diffract to 3.0 E, and we expect soon to obtain a heavy atom derivative.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119597
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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