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5R56

PanDDA analysis group deposition -- Crystal Structure of human NUDT22 in complex with N13688a

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04-1
Synchrotron siteDiamond
BeamlineI04-1
Temperature [K]100
Detector technologyPIXEL
Collection date2016-07-02
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.92819
Spacegroup nameP 21 21 21
Unit cell lengths49.590, 52.330, 101.560
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.780 - 1.510
R-factor0.1857
Rwork0.184
R-free0.21560
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)5lf9
RMSD bond length0.009
RMSD bond angle1.570
Data reduction softwareXDS
Data scaling softwareAimless (0.5.26)
Phasing softwareREFMAC
Refinement softwareREFMAC (5.8.0238)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.78050.7801.550
High resolution limit [Å]1.5106.7501.510
Rmerge0.0730.0281.582
Rmeas0.0800.0301.722
Rpim0.0310.0120.674
Total number of observations273386321619889
Number of reflections42305
<I/σ(I)>12.746.51.2
Completeness [%]99.999.799.8
Redundancy6.55.76.5
CC(1/2)0.9990.9990.521
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.52770.1M HEPES pH 7.5, 0.3M sodium/potassium phosphate, 15% PEG Smear High, 20% ethylene glycol

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