5IEY
Crystal structure of a CDK inhibitor bound to CDK2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 53.337, 71.983, 72.037 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.870 - 1.660 |
R-factor | 0.18192 |
Rwork | 0.180 |
R-free | 0.22502 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.018 |
RMSD bond angle | 1.949 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0049) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 42.870 |
High resolution limit [Å] | 1.660 |
Number of reflections | 30887 |
<I/σ(I)> | 10.69 |
Completeness [%] | 97.8 |
Redundancy | 4.25 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.8 | 293.15 | 7.25% PEG 4000, 0.2 M ammonium acetate, 0.2 M HEPES pH 7.8 |