This project involves crystallographic studies of thymidylate synthase [TS], the sole de novo pathway for dTMP synthesis in most organisms, which is an essential enzyme and target for anti-cancer/anti- proliferative drug development. We are engaged in crystallographic studies of kinetically characterized L. casei TS mutant enzymes, complexed with the substrate, directed toward understanding: i) the structural basis of substrate binding/affinity and specificity, and ii) the role of ordered water molecules in the binding pocket in substrate binding/affinity and specificity. The Computer Graphics Laboratory resource is being used for the purposes of visualizing the 3-dimensional crystal structures arising from the project and the models developed in order to understand the experimental results.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001081-22
Application #
6119215
Study Section
Project Start
1999-07-01
Project End
2000-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Kozak, John J; Gray, Harry B; Garza-López, Roberto A (2018) Relaxation of structural constraints during Amicyanin unfolding. J Inorg Biochem 179:135-145
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Sathyanarayana, Bangalore K; Li, Peng; Lin, Jian-Xin et al. (2016) Molecular Models of STAT5A Tetramers Complexed to DNA Predict Relative Genome-Wide Frequencies of the Spacing between the Two Dimer Binding Motifs of the Tetramer Binding Sites. PLoS One 11:e0160339
Forman, Stuart A; Miller, Keith W (2016) Mapping General Anesthetic Sites in Heteromeric ?-Aminobutyric Acid Type A Receptors Reveals a Potential For Targeting Receptor Subtypes. Anesth Analg 123:1263-1273

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