2CN5
Crystal structure of human Chk2 in complex with ADP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-09-07 |
Detector | ADSC CCD |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 90.865, 90.865, 92.910 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 40.830 - 2.250 |
R-factor | 0.201 |
Rwork | 0.199 |
R-free | 0.24000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1atp |
RMSD bond length | 0.018 |
RMSD bond angle | 1.726 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.820 | 2.370 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.080 | 0.470 |
Number of reflections | 21525 | |
<I/σ(I)> | 16.5 | 3.2 |
Completeness [%] | 100.0 | 100 |
Redundancy | 5.5 | 5.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.1 M HEPES PH 7.5, 0.2 M MAGNESIUM NITRATE, 8-16% (W/V) PEG 3350 |