6V1A
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 | 2018-08-22 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9537 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 149.344, 56.990, 131.184 |
Unit cell angles | 90.00, 90.87, 90.00 |
Refinement procedure
Resolution | 43.720 - 2.290 |
R-factor | 0.1882 |
Rwork | 0.187 |
R-free | 0.21370 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6bil |
RMSD bond length | 0.005 |
RMSD bond angle | 0.639 |
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] | 49.240 | 2.360 |
High resolution limit [Å] | 2.290 | 2.290 |
Rmerge | 0.104 | |
Number of reflections | 49925 | 4179 |
<I/σ(I)> | 10.7 | |
Completeness [%] | 99.1 | 91.1 |
Redundancy | 6.9 | |
CC(1/2) | 0.997 | 0.812 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.2 M trisodium citrate, 20% PEG 3350 |