6XW9
Human myelin protein P2 mutant K120S
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | EMBL/DESY, HAMBURG BEAMLINE X12 |
| Synchrotron site | EMBL/DESY, HAMBURG |
| Beamline | X12 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2011-03-24 |
| Detector | RAYONIX MX-225 |
| Wavelength(s) | 0.91 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 63.680, 63.680, 101.400 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 40.000 - 2.900 |
| R-factor | 0.2125 |
| Rwork | 0.210 |
| R-free | 0.25700 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2wut |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.531 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX (dev_2247) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.000 | 2.980 |
| High resolution limit [Å] | 2.900 | 2.900 |
| Rmeas | 0.144 | 1.145 |
| Number of reflections | 4976 | 336 |
| <I/σ(I)> | 10.5 | 1.8 |
| Completeness [%] | 99.6 | 97.4 |
| Redundancy | 7.2 | |
| CC(1/2) | 0.998 | 0.859 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5 | 277 | 30% PEG 6000, 0.1 M citrate pH 5.0 |






