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5R59

PanDDA analysis group deposition -- Crystal Structure of human NUDT22 in complex with N13441a

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 lengths49.660, 52.180, 101.760
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.880 - 2.110
R-factor0.1964
Rwork0.192
R-free0.26970
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)5lf9
RMSD bond length0.008
RMSD bond angle1.541
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]52.18052.1802.160
High resolution limit [Å]2.1109.4402.110
Rmerge0.1830.0281.385
Rmeas0.2000.0311.508
Rpim0.0780.0130.590
Total number of observations10195212347437
Number of reflections15832
<I/σ(I)>8.843.71.5
Completeness [%]99.898.6100
Redundancy6.45.56.4
CC(1/2)0.9960.9990.515
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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