3QK5
Crystal structure of fatty acid amide hydrolase with small molecule inhibitor
Summary for 3QK5
Entry DOI | 10.2210/pdb3qk5/pdb |
Related | 3QJ8 3QJ9 3QKV |
Descriptor | Fatty-acid amide hydrolase 1, (3-{(3R)-1-[4-(1-benzothiophen-2-yl)pyrimidin-2-yl]piperidin-3-yl}-2-methyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetonitrile, 1,2-ETHANEDIOL, ... (5 entities in total) |
Functional Keywords | protein-inhibitor complex, faah, fatty-acid amide hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Rattus norvegicus (rat) |
Cellular location | Endoplasmic reticulum membrane; Single-pass membrane protein: P97612 |
Total number of polymer chains | 2 |
Total formula weight | 131138.64 |
Authors | Min, X.,Walker, N.P.C.,Wang, Z. (deposition date: 2011-01-31, release date: 2011-04-06, Last modification date: 2023-09-13) |
Primary citation | Gustin, D.J.,Ma, Z.,Min, X.,Li, Y.,Hedberg, C.,Guimaraes, C.,Porter, A.C.,Lindstrom, M.,Lester-Zeiner, D.,Xu, G.,Carlson, T.J.,Xiao, S.,Meleza, C.,Connors, R.,Wang, Z.,Kayser, F. Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors. Bioorg.Med.Chem.Lett., 21:2492-2496, 2011 Cited by PubMed: 21392988DOI: 10.1016/j.bmcl.2011.02.052 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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