9OBF
Crystal structure of HLA*02:01 with the 11-mer TP53 peptide GLAPPQHLIRV
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 19-ID |
| Synchrotron site | NSLS-II |
| Beamline | 19-ID |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2024-02-20 |
| Detector | DECTRIS EIGER2 XE 9M |
| Wavelength(s) | 0.97857 |
| Spacegroup name | P 63 2 2 |
| Unit cell lengths | 161.130, 161.130, 330.280 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 47.970 - 3.250 |
| R-factor | 0.1949 |
| Rwork | 0.194 |
| R-free | 0.21170 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.501 |
| Data reduction software | HKL-3000 |
| Data scaling software | HKL-3000 |
| Phasing software | HKL-3000 |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.000 | 3.310 |
| High resolution limit [Å] | 3.250 | 3.250 |
| Rmerge | 0.197 | 1.142 |
| Rmeas | 0.206 | |
| Rpim | 0.058 | 0.369 |
| Number of reflections | 40748 | 1974 |
| <I/σ(I)> | 9.5 | 1.6 |
| Completeness [%] | 99.8 | 99.9 |
| Redundancy | 12.4 | 10 |
| CC(1/2) | 0.989 | 0.741 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7 | 289 | Screen MCSG4 - condition C9: 0.1 M Bis-Tris Propane:HCl and 60% (v/v) Microlytic mix; (Microlytic mix: 1.8305 M Malonic Acid, 0.25 M Ammonium Citrate Tribasic, 0.12 M Succinic Acid, 0.3 M DL-Malic Acid, 0.4 M Sodium Acetate Trihydrate, 0.5 M Sodium Formate, 0.16 M Ammonium Tartrate Dibasic) |






