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 |






