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3VFP

crystal structure of HLA B*3508 LPEP158G, HLA mutant Gly158

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX1
Synchrotron siteAustralian Synchrotron
BeamlineMX1
Temperature [K]100
Detector technologyCCD
Collection date2011-04-08
DetectorADSC QUANTUM 210
Wavelength(s)0.9536
Spacegroup nameP 21 21 21
Unit cell lengths50.993, 81.505, 110.899
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution19.481 - 1.850
R-factor0.2104
Rwork0.207
R-free0.26590
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1zhk
RMSD bond length0.007
RMSD bond angle1.004
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.7.1_743)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]1.800
High resolution limit [Å]1.7001.700
Rmerge0.0790.198
Number of reflections3328
<I/σ(I)>16.558.12
Completeness [%]70.441.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.62930.2M ammonium acetate, 16% PEG 4K, 0.1M sodium citrate pH5.6, vapor diffusion, hanging drop, temperature 293K

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