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4F7L

Crystal structure of human CDK8/CYCC in complex with compound 2 (tert-butyl [3-({[3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-yl]carbamoyl}amino)propyl]carbamate)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X06SA
Synchrotron siteSLS
BeamlineX06SA
Temperature [K]100
Detector technologyPIXEL
Collection date2011-09-07
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.99986
Spacegroup nameP 21 21 21
Unit cell lengths71.819, 71.242, 171.705
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution85.850 - 2.900
R-factor0.2255
Rwork0.224
R-free0.26998
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3rgf
RMSD bond length0.011
RMSD bond angle1.283
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareMOLREP
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]85.8503.090
High resolution limit [Å]2.9002.900
Rmerge0.0810.432
Number of reflections19174
Completeness [%]94.984.3
Redundancy3.93.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.9293.1520% PEG3350, 0.2 M sodium formate, pH 6.9, VAPOR DIFFUSION, HANGING DROP, temperature 293.15K

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