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4WIL

Crystal structure of DCoH2 S51T

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-BM
Synchrotron siteAPS
Beamline22-BM
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2011-08-17
DetectorMAR scanner 345 mm plate
Wavelength(s)1.00
Spacegroup nameP 31 2 1
Unit cell lengths57.729, 57.729, 115.064
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution24.997 - 1.360
R-factor0.1587
Rwork0.158
R-free0.17460
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ru0
RMSD bond length0.006
RMSD bond angle1.045
Refinement softwarePHENIX ((phenix.refine: 1.6.4_486))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0001.380
High resolution limit [Å]1.3601.360
Rmerge0.953
Number of reflections48837
<I/σ(I)>58.12.98
Completeness [%]97.896.4
Redundancy10.79.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1EVAPORATION7.52910.1M Tris, 8% PEG 8,000 mixing 0.5 ul protein and 1 ul reservoir

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