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2CN8

Crystal structure of human Chk2 in complex with debromohymenialdisine

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX14.1
Synchrotron siteSRS
BeamlinePX14.1
Temperature [K]100
Detector technologyCCD
Collection date2005-09-26
DetectorADSC CCD
Spacegroup nameP 32 2 1
Unit cell lengths88.650, 88.650, 88.897
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution76.700 - 2.700
R-factor0.207
Rwork0.204
R-free0.27100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2cn5
RMSD bond angle2.226
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.6502.850
High resolution limit [Å]2.7002.700
Rmerge0.0700.530
Number of reflections11261
<I/σ(I)>162.8
Completeness [%]98.7100
Redundancy4.34.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
10.1 M HEPES PH 7.5, 0.2 M MAGNESIUM NITRATE,8-16% (W/V) PEG 3350

222624

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