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1PXK

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

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7A
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7A
Temperature [K]100
Detector technologyCCD
Collection date2003-01-01
DetectorADSC QUANTUM 4
Wavelength(s)0.97
Spacegroup nameP 21 21 21
Unit cell lengths52.744, 71.948, 70.525
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution19.830 - 2.800
R-factor0.208
Rwork0.208
R-free0.26600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1hcl
RMSD bond length0.007
RMSD bond angle22.900

*

Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareMOLREP
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.980
High resolution limit [Å]2.8002.800
Rmerge0.0890.597
Total number of observations20559

*

Number of reflections6931
<I/σ(I)>7.81.1
Completeness [%]99.399.3
Redundancy3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.8277PEG 6000, NA-HEPES, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 277K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein7-8 (mg/ml)
21reservoirPEG600015 (%)
31reservoirsodium HEPES100 (mM)pH7.8-8.2

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数据于2024-04-17公开中

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