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Article
Nature Structural Biology  3, 927 - 933 (1996)
doi:10.1038/nsb1196-927

Flexibility of the NSAID binding site in the structure of human cyclooxygenase-2

Christine Luong1, Aaron Miller1, Jim Barnett1, Joan Chow1, Chakk Ramesha1 & Michelle F. Browner1, 2

  1Inflammatory Diseases Unit, Roche Bioscience 3401 Hillview Ave, Palo Alto, California 94303, USA

  2michelle.browner@roche.com

The first crystal structure of human cyclooxygenase-2, in the presence of a selective inhibitor, is similar to that of cyclooxygenase-1. The structure of the NSAID binding site is also well conserved, although there are differences in its overall size and shape which may be exploited for the further development of selective COX-2 inhibitors. A second COX-2 structure with a different bound inhibitor displays a new, open conformation at the bottom of the NSAID binding site, without significant changes in other regions of the COX-2 structure. These two COX-2 structures provide evidence for the flexible nature of cyclooxygenase, revealing details about how substrate and inhibitor may gain access to the cyclooxygenase active site from within the membrane.

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