6V18
immune receptor complex
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 | 2019-02-20 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9537 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 147.878, 56.266, 128.915 |
Unit cell angles | 90.00, 91.35, 90.00 |
Refinement procedure
Resolution | 48.830 - 2.350 |
R-factor | 0.1949 |
Rwork | 0.193 |
R-free | 0.23070 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6bil |
RMSD bond length | 0.007 |
RMSD bond angle | 0.850 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.833 | 2.430 |
High resolution limit [Å] | 2.350 | 2.350 |
Rmerge | 0.137 | 1.446 |
Number of reflections | 44286 | 4318 |
<I/σ(I)> | 9.3 | |
Completeness [%] | 99.2 | |
Redundancy | 7.1 | |
CC(1/2) | 0.996 | 0.685 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.2 M trisodium citrate, 20% PEG 3350 |