6D5Y
Crystal structure of ERK2 G169D mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 93 |
Detector technology | CCD |
Collection date | 2011-01-12 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.03317 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 44.870, 65.400, 116.790 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.860 |
R-factor | 0.2218 |
Rwork | 0.220 |
R-free | 0.27190 |
RMSD bond length | 0.002 |
RMSD bond angle | 0.517 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.870 |
High resolution limit [Å] | 2.860 | 2.860 |
Number of reflections | 57377 | |
<I/σ(I)> | 18.5 | |
Completeness [%] | 92.3 | |
Redundancy | 7.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 277 | 20% PEG 3350, 10% isopropanol, and 0.1 M Hepes pH 7.5 |