Details

Autor(en) / Beteiligte

• Mileni, Mauro
• Garfunkle, Joie
• Ezzili, Cyrine
• Kimball, F. Scott
• Cravatt, Benjamin F
• Stevens, Raymond C
• Boger, Dale L

Titel

X-ray Crystallographic Analysis of α-Ketoheterocycle Inhibitors Bound to a Humanized Variant of Fatty Acid Amide Hydrolase

Ist Teil von

• Journal of medicinal chemistry, 2010-01, Vol.53 (1), p.230-240

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2010

Quelle

MEDLINE

Beschreibungen/Notizen

• Three cocrystal X-ray structures of the α-ketoheterocycle inhibitors 3−5 bound to a humanized variant of fatty acid amide hydrolase (FAAH) are disclosed and comparatively discussed alongside those of 1 (OL-135) and its isomer 2. These five X-ray structures systematically probe each of the three active site regions key to substrate or inhibitor binding: (1) the conformationally mobile acyl chain-binding pocket and membrane access channel responsible for fatty acid amide substrate and inhibitor acyl chain binding, (2) the atypical active site catalytic residues and surrounding oxyanion hole that covalently binds the core of the α-ketoheterocycle inhibitors captured as deprotonated hemiketals mimicking the tetrahedral intermediate of the enzyme-catalyzed reaction, and (3) the cytosolic port and its uniquely important imbedded ordered water molecules and a newly identified anion binding site. The detailed analysis of their key active site interactions and their implications on the interpretation of the available structure−activity relationships are discussed providing important insights for future design.