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3PE4

Structure of human O-GlcNAc transferase and its complex with a peptide substrate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X25
Synchrotron siteNSLS
BeamlineX25
Temperature [K]100
Detector technologyCCD
Collection date2009-11-15
DetectorADSC QUANTUM 315
Wavelength(s)1.000
Spacegroup nameI 1 2 1
Unit cell lengths98.600, 136.700, 153.500
Unit cell angles90.00, 102.90, 90.00
Refinement procedure
Resolution30.000 - 1.950
R-factor0.2254
Rwork0.224
R-free0.25180
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.007
RMSD bond angle1.050
Data reduction softwareiMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwarePHENIX ((phenix.refine: 1.6.1_357))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.060
High resolution limit [Å]1.9501.950
Number of reflections141571
<I/σ(I)>8.44.7
Completeness [%]98.494.5
Redundancy3.12.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP72981.6M Lithium Sulfate, 0.1M Bis Tris Propane pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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