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3PE3

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

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X29A
Synchrotron siteNSLS
BeamlineX29A
Temperature [K]100
Detector technologyCCD
Collection date2009-09-08
DetectorADSC QUANTUM 315
Wavelength(s)1.0809
Spacegroup nameP 3 2 1
Unit cell lengths273.400, 273.400, 142.800
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution48.583 - 2.780
R-factor0.1852
Rwork0.185
R-free0.21770
Structure solution methodMIR
RMSD bond length0.003
RMSD bond angle0.707
Data reduction softwareiMOSFLM
Data scaling softwareSCALA
Phasing softwareSHARP
Refinement softwarePHENIX ((phenix.refine: 1.6.1_357))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.930
High resolution limit [Å]2.7802.780
Number of reflections154231
<I/σ(I)>8.43
Completeness [%]98.295.1
Redundancy3.33.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.52981.45 M Potassium Phosphate Dibasic, 8 mM EDTA, 1% xylitol, pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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