3K7F
Crystal Structure Analysis of a Phenhexyl/Oxazole/Carboxypyridine alpha-Ketoheterocycle Inhibitor Bound to a Humanized Variant of Fatty Acid Amide Hydrolase'
Summary for 3K7F
Entry DOI | 10.2210/pdb3k7f/pdb |
Related | 2wj1 2wj2 |
Descriptor | Fatty-acid amide hydrolase 1, 6-[2-(7-phenylheptanoyl)-1,3-oxazol-5-yl]pyridine-2-carboxylic acid, CHLORIDE ION, ... (5 entities in total) |
Functional Keywords | protein-inhibitor complex, faah, oxazole, hydrolase, membrane, transmembrane |
Biological source | Rattus norvegicus (rat) |
Cellular location | Endoplasmic reticulum membrane; Single-pass membrane protein: P97612 |
Total number of polymer chains | 2 |
Total formula weight | 127038.61 |
Authors | Mileni, M.,Stevens, R.C.,Boger, D.L. (deposition date: 2009-10-13, release date: 2009-12-01, Last modification date: 2023-09-06) |
Primary citation | Mileni, M.,Garfunkle, J.,Ezzili, C.,Kimball, F.S.,Cravatt, B.F.,Stevens, R.C.,Boger, D.L. X-ray crystallographic analysis of alpha-ketoheterocycle inhibitors bound to a humanized variant of fatty acid amide hydrolase. J.Med.Chem., 53:230-240, 2010 Cited by PubMed: 19924997DOI: 10.1021/jm9012196 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.95 Å) |
Structure validation
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