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4DO3

Structure of FAAH with a non-steroidal anti-inflammatory drug

Summary for 4DO3
Entry DOI10.2210/pdb4do3/pdb
Related1M5T 2VYA 3LJ7
DescriptorFatty-acid amide hydrolase 1, CHLORIDE ION, CYCLOHEXANE AMINOCARBOXYLIC ACID, ... (5 entities in total)
Functional Keywordsamidase, hydrolase, anandamide, nsaid, drug, cox, inhibitor, inflammation, pain, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceRattus norvegicus (rat)
Cellular locationEndoplasmic reticulum membrane; Single-pass membrane protein: P97612
Total number of polymer chains2
Total formula weight126614.04
Authors
Garau, G. (deposition date: 2012-02-09, release date: 2013-01-23, Last modification date: 2023-09-13)
Primary citationBertolacci, L.,Romeo, E.,Veronesi, M.,Magotti, P.,Albani, C.,Dionisi, M.,Lambruschini, C.,Scarpelli, R.,Cavalli, A.,De Vivo, M.,Piomelli, D.,Garau, G.
A Binding Site for Nonsteroidal Anti-inflammatory Drugs in Fatty Acid Amide Hydrolase.
J.Am.Chem.Soc., 135:22-25, 2013
Cited by
PubMed: 23240907
DOI: 10.1021/ja308733u
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.25 Å)
Structure validation

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