UvrA is a component of the bacterial UvrABC DNA nucleotide excision repair system. The primary function of UvrA is to scan the DNA for lesions, which can vary greatly in their conformation and chemical structure, eventually initiating DNA repair. UvrA has a molecular weight of 104 kDa, is functional as a dimer and contains 2 zinc fingers, 1 helix-turn-helix motif and 2 ATP binding cassettes (ABC motifs). Its sequence homology to classical ABC transporters suggests common mechanisms and structural features for coupling ATP hydrolysis to mechanical actions. We have crystallized UvrA in the presence of ADP in spacegroup P212121 with unit cell dimensions of a = 152, b = 182, c = 225 E. The crystals grow to maximum dimensions of 2.5 x 1.0 x 0.03 mm and diffract to about 4 E at 130 K using rotating-anode X-ray generators and to about 3 E using synchrotron radiation (CHESS, ESRF).

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119495
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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