43SK
Crystal structure of H2-Q9/VP2.139 peptide H1A mutant
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-07-14 |
| Detector | STFC Large Pixel Detector |
| Wavelength(s) | 0.95373 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 54.619, 56.799, 119.314 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 41.140 - 2.030 |
| R-factor | 0.2106 |
| Rwork | 0.209 |
| R-free | 0.24610 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.516 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.21.2_5419: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 41.140 | 2.080 |
| High resolution limit [Å] | 2.030 | 2.030 |
| Rpim | 0.024 | 0.302 |
| Number of reflections | 24708 | 24708 |
| <I/σ(I)> | 16 | 2.4 |
| Completeness [%] | 99.9 | |
| Redundancy | 7.3 | |
| CC(1/2) | 0.999 | 0.754 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7 | 293.15 | 0.2 M ammonium acetate, 0.1M HEPES pH 7.0, 20% (w/v) PEG 3350 |






