4BCN
Structure of CDK2 in complex with cyclin A and a 2-amino-4-heteroaryl- pyrimidine inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 74.050, 135.080, 148.190 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.915 - 2.100 |
R-factor | 0.1856 |
Rwork | 0.184 |
R-free | 0.21910 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.004 |
RMSD bond angle | 0.774 |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.910 | 2.210 |
High resolution limit [Å] | 2.070 | 2.100 |
Rmerge | 0.080 | 0.550 |
Number of reflections | 87330 | |
<I/σ(I)> | 6.68 | 1.38 |
Completeness [%] | 99.9 | 99.9 |
Redundancy | 4.02 | 4.05 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7 | COCRYSTALS WERE GROWN IN 1-1.25M AMMONIUM SULFATE, 0.5-0.9M KCL, 100MM HEPES, PH 7.0, 5MM DTT AND IN THE PRESENCE OF COMPOUND. |