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5R52

PanDDA analysis group deposition -- Crystal Structure of human NUDT22 in complex with N14004a

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 lengths49.570, 52.370, 101.880
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution46.620 - 1.480
R-factor0.1888
Rwork0.187
R-free0.21750
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)5lf9
RMSD bond length0.010
RMSD bond angle1.658
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]46.58046.5801.520
High resolution limit [Å]1.4806.6201.480
Rmerge0.0790.0361.692
Rmeas0.0860.0391.849
Rpim0.0340.0160.738
Total number of observations291337332620036
Number of reflections45068
<I/σ(I)>11.539.21.1
Completeness [%]99.999.799.8
Redundancy6.55.66.1
CC(1/2)0.9990.9980.474
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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