9MEG
Conformational flexibility in HLA-B8: peptide tuning structural and dynamical changes
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | EMBL/DESY, HAMBURG BEAMLINE X31 |
| Synchrotron site | EMBL/DESY, HAMBURG |
| Beamline | X31 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2024-01-31 |
| Detector | MAR CCD 300 mm |
| Wavelength(s) | 0.87313 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 50.930, 81.440, 110.820 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 27.580 - 1.610 |
| R-factor | 0.20215 |
| Rwork | 0.201 |
| R-free | 0.22657 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.876 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0425) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.270 | 1.650 |
| High resolution limit [Å] | 1.610 | 1.610 |
| Rmerge | 0.099 | 0.330 |
| Number of reflections | 56986 | 15283 |
| <I/σ(I)> | 10.7 | 3.3 |
| Completeness [%] | 99.5 | 99.5 |
| Redundancy | 7.5 | 6.5 |
| CC(1/2) | 0.995 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 298 | 50% PEG4000, 20% citrate acid pH5.5, 0.1M ammonium acetate |






