8TBV
Human Class I MHC HLA-A2 in complex with sorting nexin 24 (127-135) neoantigen KLSHQLVLL
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-E |
| Synchrotron site | APS |
| Beamline | 24-ID-E |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-10-23 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 62.226, 86.726, 79.268 |
| Unit cell angles | 90.00, 90.07, 90.00 |
Refinement procedure
| Resolution | 62.230 - 2.640 |
| R-factor | 0.2337 |
| Rwork | 0.229 |
| R-free | 0.27440 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.421 |
| Data reduction software | DIALS (2.2.10) |
| Data scaling software | DIALS (2.2.10) |
| Phasing software | PHENIX (1.20rc3_4406) |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 62.230 | 2.734 |
| High resolution limit [Å] | 2.640 | 2.640 |
| Number of reflections | 23797 | 2209 |
| <I/σ(I)> | 4.32 | |
| Completeness [%] | 92.0 | 88.75 |
| Redundancy | 6.6 | |
| CC(1/2) | 0.944 | 0.649 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 277.15 | Purified protein complexes were concentrated to 7.4 mg/mL before crystallization. The crystals were grown in 12.5% PEG 4000 and 0.1 M MES (pH 6.5) via hanging drop vapor diffusion. Crystals were harvested and cryoprotected in 8% glycerol/92% mother liquor and immediately stored in liquid nitrogen |






