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3U1K

Crystal structure of human PNPase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSRRC BEAMLINE BL13C1
Synchrotron siteNSRRC
BeamlineBL13C1
Temperature [K]100
Detector technologyCCD
Collection date2011-02-24
DetectorRAYONIX MX300HE
Wavelength(s)1.0
Spacegroup nameH 3
Unit cell lengths289.753, 289.753, 92.785
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution28.500 - 2.130
R-factor0.1821
Rwork0.180
R-free0.22300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3gcm
RMSD bond length0.007
RMSD bond angle1.071
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwarePHENIX ((phenix.refine: 1.7.1_743))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.210
High resolution limit [Å]2.1302.130
Rmerge0.0460.311
Number of reflections162293
<I/σ(I)>30.84.7
Completeness [%]100.0100
Redundancy3.23.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP529810%(v/v) 2-Propanol, 0.1M Sodium citrate tribasic dihydrate, 26%(v/v) Polyethylene glycol 400 , pH 5.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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