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3PPM

Crystal Structure of a Noncovalently Bound alpha-Ketoheterocycle Inhibitor (Phenhexyl/Oxadiazole/Pyridine) to a Humanized Variant of Fatty Acid Amide Hydrolase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL11-1
Synchrotron siteSSRL
BeamlineBL11-1
Temperature [K]100
Detector technologyCCD
Collection date2008-11-21
DetectorMARMOSAIC 325 mm CCD
Wavelength(s)0.97945
Spacegroup nameP 32 2 1
Unit cell lengths103.692, 103.692, 254.705
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution33.940 - 1.780
R-factor0.1525
Rwork0.151
R-free0.17640
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2wj1
RMSD bond length0.007
RMSD bond angle1.081
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((phenix.refine: 1.6.4_486))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]33.9401.810
High resolution limit [Å]1.7801.780
Number of reflections151855
<I/σ(I)>202
Completeness [%]99.699
Redundancy3.92.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION5.528730% PEG400, 100 mM Mes pH 5.5, 100 mM KCl, 200 mM NaCl, 100 mM NaF, and 8% polypropylene glycol-P400, VAPOR DIFFUSION, temperature 287K

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