2CN8
Crystal structure of human Chk2 in complex with debromohymenialdisine
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SRS BEAMLINE PX14.1 |
Synchrotron site | SRS |
Beamline | PX14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-09-26 |
Detector | ADSC CCD |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 88.650, 88.650, 88.897 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 76.700 - 2.700 |
R-factor | 0.207 |
Rwork | 0.204 |
R-free | 0.27100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2cn5 |
RMSD bond angle | 2.226 |
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] | 39.650 | 2.850 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.070 | 0.530 |
Number of reflections | 11261 | |
<I/σ(I)> | 16 | 2.8 |
Completeness [%] | 98.7 | 100 |
Redundancy | 4.3 | 4.3 |
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 |