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Study of arachidonoyl specificity in two enzymes of the PI cycle.

J Mol Biol.. 2011-06;  409(2):101-12
Shulga YV, Topham MK, Epand RM. 1 Department of Biochemistry and Biomedical Sciences, McMaster University, 1200 Main Street West, Hamilton, Ontario L8N 3Z5, Canada2 Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope, Salt Lake City, UT 84112, USA
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摘要

We identified a conserved pattern of residues L-X(3-4)-R-X(2)-L-X(4)-G, in which -X(n)-is n residues of any amino acid, in two enzymes acting on the polyunsaturated fatty acids, diacylglycerol kinase epsilon (DGKε) and phosphatidylinositol-4-phosphate-5-kinase Iα (PIP5K Iα). DGKε is the only one of the 10 mammalian isoforms of DGK that exhibits arachidonoyl specificity and is the only isoform with the motif mentioned above. Mutations of the essential residues in this motif result in the loss of arachidonoyl specificity. Furthermore, DGKα can be converted to an enzyme having this motif by substituting only one residue. When DGKα was mutated so that it gained the motif, the... More

关键词

diacylglycerol kinase; acyl chain specificity; phosphatidylinositol-4-phosphate-5-kinase; arachidonic acid; PI-cycling