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1PXP

HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR N-[4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-N',N'-dimethyl-benzene-1,4-diamine

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX9.6
Synchrotron siteSRS
BeamlinePX9.6
Temperature [K]100
Detector technologyCCD
DetectorADSC QUANTUM 4
Wavelength(s)0.87
Spacegroup nameP 21 21 21
Unit cell lengths53.337, 71.794, 71.414
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution23.600 - 2.300
R-factor0.23
Rwork0.230
R-free0.27300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1hcl
RMSD bond length0.006
RMSD bond angle1.200
Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareMOLREP
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]23.0002.440
High resolution limit [Å]2.3002.300
Rmerge0.5000.148
Number of reflections12686
<I/σ(I)>4.94.9
Completeness [%]98.796.7
Redundancy3.43.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.8277PEG 6000, NA-HEPES, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 277K

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