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Structure paper

TitleCrystal structure of fatty acid amide hydrolase bound to the carbamate inhibitor URB597: discovery of a deacylating water molecule and insight into enzyme inactivation
Journal, issue, pagesJ. Mol. Biol., Vol. 400, Page 743-754, Year 2010
Publish dateJan 25, 2010 (structure data deposition date)
AuthorsMileni, M. / Kamtekar, S. / Wood, D.C. / Benson, T.E. / Cravatt, B.F. / Stevens, R.C.
External linksJ. Mol. Biol. / PubMed:20493882
MethodsX-ray diffraction
Resolution2.3 - 2.42 Å
Structure data

PDB-3lj6:
3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH THE DRUG-LIKE UREA INHIBITOR PF-3845 at 2.42A RESOLUTION
Method: X-RAY DIFFRACTION / Resolution: 2.42 Å

PDB-3lj7:
3D-crystal structure of humanized-rat fatty acid amide hydrolase (FAAH) conjugated with Carbamate inhibitor URB597
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

Chemicals

ChemComp-PIX:
4-(3-{[5-(trifluoromethyl)pyridin-2-yl]oxy}benzyl)piperidine-1-carboxylic acid

ChemComp-CL:
Unknown entry

ChemComp-HOH:
WATER

ChemComp-OHO:
CYCLOHEXANE AMINOCARBOXYLIC ACID

Source
  • rattus norvegicus (Norway rat)
KeywordsHYDROLASE / protein-inhibitor complex / FAAH / fatty acid amide hydrolase / urea / inhibitor / covalent / Endoplasmic reticulum / Golgi apparatus / Membrane / Transmembrane / carbamate

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