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3Q7D

Structure of (R)-naproxen bound to mCOX-2.

Summary for 3Q7D
Entry DOI10.2210/pdb3q7d/pdb
DescriptorProstaglandin G/H synthase 2, 2-acetamido-2-deoxy-beta-D-glucopyranose, PROTOPORPHYRIN IX CONTAINING FE, ... (7 entities in total)
Functional Keywordsprostaglandin h2 synthase, cyclooxygenase-2, naproxen, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
Biological sourceMus musculus (mouse)
Total number of polymer chains2
Total formula weight139661.33
Authors
Duggan, K.C.,Hermanson, D.J.,Musee, J.,Prusakiewicz, J.J.,Scheib, J.,Carter, B.D.,Banerjee, S.,Marnett, L.J. (deposition date: 2011-01-04, release date: 2011-11-09, Last modification date: 2024-11-20)
Primary citationDuggan, K.C.,Hermanson, D.J.,Musee, J.,Prusakiewicz, J.J.,Scheib, J.L.,Carter, B.D.,Banerjee, S.,Oates, J.A.,Marnett, L.J.
(R)-Profens are substrate-selective inhibitors of endocannabinoid oxygenation by COX-2.
Nat.Chem.Biol., 7:803-809, 2011
Cited by
PubMed Abstract: Cyclooxygenase-2 (COX-2) catalyzes the oxygenation of arachidonic acid and the endocannabinoids 2-arachidonoylglycerol and arachidonoylethanolamide. Evaluation of a series of COX-2 inhibitors revealed that many weak competitive inhibitors of arachidonic acid oxygenation are potent inhibitors of endocannabinoid oxygenation. (R) enantiomers of ibuprofen, naproxen and flurbiprofen, which are considered to be inactive as COX-2 inhibitors, are potent 'substrate-selective inhibitors' of endocannabinoid oxygenation. Crystal structures of the COX-2–(R)-naproxen and COX-2–(R)-flurbiprofen complexes verified this unexpected binding and defined the orientation of the (R) enantiomers relative to (S) enantiomers. (R)-Profens selectively inhibited endocannabinoid oxygenation by lipopolysaccharide-stimulated dorsal root ganglion (DRG) cells. Substrate-selective inhibition provides new tools for investigating the role of COX-2 in endocannabinoid oxygenation and a possible explanation for the ability of (R)-profens to maintain endocannabinoid tone in models of neuropathic pain.
PubMed: 22053353
DOI: 10.1038/nchembio.663
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

237735

数据于2025-06-18公开中

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