5L2W
The X-ray co-crystal structure of human CDK2/CyclinE and Dinaciclib.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 17-ID |
Synchrotron site | APS |
Beamline | 17-ID |
Temperature [K] | 98.15 |
Detector technology | PIXEL |
Collection date | 2015-11-09 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 100.307, 100.307, 151.857 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.000 - 2.800 |
R-factor | 0.2019 |
Rwork | 0.200 |
R-free | 0.24630 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 1w98 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.150 |
Data scaling software | Aimless |
Phasing software | BUSTER |
Refinement software | BUSTER (2.11.4) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 45.000 |
High resolution limit [Å] | 2.800 |
Number of reflections | 19770 |
<I/σ(I)> | 22.9 |
Completeness [%] | 99.9 |
Redundancy | 12.76 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 286.15 | PEG20K, 180mM Mg(HCO2)2, 0.1M MES pH 6.0 |