9BLA
KIR3DL1*086 in complex with HLA-A*24:02 presenting the NEF peptide
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 | 2024-03-11 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9536 |
| Spacegroup name | P 1 |
| Unit cell lengths | 50.682, 61.790, 67.473 |
| Unit cell angles | 93.73, 100.68, 108.34 |
Refinement procedure
| Resolution | 46.960 - 3.000 |
| R-factor | 0.2024 |
| Rwork | 0.200 |
| R-free | 0.24770 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.532 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.21rc1_5058) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.960 | 3.180 |
| High resolution limit [Å] | 3.000 | 3.000 |
| Rmerge | 0.063 | 0.355 |
| Rpim | 0.045 | |
| Number of reflections | 14821 | 2422 |
| <I/σ(I)> | 5.8 | 2.8 |
| Completeness [%] | 97.9 | |
| Redundancy | 2.8 | |
| CC(1/2) | 0.996 | 0.965 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 294 | 14% PEG 3350, 2% tacsimate pH 5.0, 0.1 M tri-sodium citrate pH 5.6 |






