7K80
KIR3DL1*001 in complex with HLA-A*24:02 presenting the RYPLTFGW peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-05-05 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.954 |
Spacegroup name | P 1 |
Unit cell lengths | 51.265, 85.017, 94.832 |
Unit cell angles | 82.47, 85.97, 77.92 |
Refinement procedure
Resolution | 40.000 - 2.400 |
R-factor | 0.2006 |
Rwork | 0.198 |
R-free | 0.24910 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3vh8 |
RMSD bond length | 0.004 |
RMSD bond angle | 0.759 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((1.17.1_3660: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 43.090 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.060 | 0.470 |
Number of reflections | 58740 | 3718 |
<I/σ(I)> | 13.4 | |
Completeness [%] | 97.0 | 91 |
Redundancy | 1.9 | 1.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 298 | 14% PEG 3350, 2% tacsimate, pH 5.0, and 0.1 M trisodium citrate, pH 5.6 |