1. Biochemistry of Protein Isoprenylation. It has recently been shown that a product(s) derived from mevalonic acid becomes attached to proteins in animal cells. The role of this novel post-translational lipidation will be probed. The chemical structure of the lipid, its mode of attachment to proteins and the enzymology of the modification will be studied. 2. Enzymology of Phospholipase A2. We will continue to study the inhibition of phospholipase A2 using carefully constructed assay systems. The inhibition by lipocortins, analogs of manoalide, and lysocardiolipins will be studied in detail. 3. Inhibition of Diaminopimelic Acid Epimerase. Beta-fluorinated analogs of diaminopimelic acid are potent inhibitors of bacterial diaminopimelic acid. The mechanism of the inhibition will be studied in detail.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Modified Research Career Development Award (K04)
Project #
5K04GM000562-05
Application #
2165954
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1990-09-01
Project End
1995-08-31
Budget Start
1994-09-01
Budget End
1995-08-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Washington
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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