1diy

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1diy, resolution 3.0Å

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CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND IN THE CYCLOOXYGENASE ACTIVE SITE OF PGHS-1

Overview

Prostaglandin H synthase-1 and -2 (PGHS-1 and -2) catalyze the committed, step in prostaglandin synthesis and are targets for nonsteroidal, anti-inflammatory drugs (NSAIDs) like aspirin. We have determined the, structure of PGHS-1 at 3 angstrom resolution with arachidonic acid (AA), bound in a chemically productive conformation. The fatty acid adopts an, extended L-shaped conformation that positions the 13proS hydrogen of AA, for abstraction by tyrosine-385, the likely radical donor. A space also, exists for oxygen addition on the antarafacial surface of the carbon in, the 11-position (C-11). While this conformation allows endoperoxide, formation between C-11 and C-9, it also implies that a subsequent, conformational rearrangement must occur to allow formation of the C-8/C-12, bond and to position C-15 for attack by a second molecule of oxygen.

About this Structure

1DIY is a Single protein structure of sequence from Ovis aries with BOG, COH and ACD as ligands. Active as Prostaglandin-endoperoxide synthase, with EC number 1.14.99.1 Full crystallographic information is available from OCA.

Reference

The productive conformation of arachidonic acid bound to prostaglandin synthase., Malkowski MG, Ginell SL, Smith WL, Garavito RM, Science. 2000 Sep 15;289(5486):1933-7. PMID:10988074

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