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5L2I

The X-ray co-crystal structure of human CDK6 and Palbociclib.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 17-ID
Synchrotron siteAPS
Beamline17-ID
Temperature [K]98.15
Detector technologyPIXEL
Collection date2013-08-19
DetectorDECTRIS PILATUS3 6M
Wavelength(s)1.0
Spacegroup nameI 4
Unit cell lengths101.749, 101.749, 60.778
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution37.000 - 2.750
R-factor0.2346
Rwork0.226
R-free0.30370
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)3nux
RMSD bond length0.010
RMSD bond angle1.160
Data scaling softwareAimless (0.5.21)
Phasing softwareBUSTER
Refinement softwareBUSTER (2.11.4)
Data quality characteristics
 Overall
Low resolution limit [Å]50.000
High resolution limit [Å]2.750
Number of reflections8324
<I/σ(I)>14.6
Completeness [%]100.0
Redundancy6.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP286.151:1 (protein to well buffer) with well buffer containing: 0.1 M MES pH 6.0, 70 - 80 mM NH4NO3, 10 - 15% polyethyleneglycol 3350.

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