6MRA
Diversity in the type II Natural Killer T cell receptor repertoire and antigen specificity leads to differing CD1d docking strategies
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 | 2014-03-14 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 49.447, 74.229, 115.578 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.460 - 1.700 |
R-factor | 0.183 |
Rwork | 0.181 |
R-free | 0.21900 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.060 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | BUSTER (2.10.3) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.600 | 1.790 |
High resolution limit [Å] | 1.700 | 1.700 |
Rpim | 0.029 | 0.308 |
Number of reflections | 47656 | 6830 |
<I/σ(I)> | 16.2 | |
Completeness [%] | 100.0 | 99.8 |
Redundancy | 8.9 | 2.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4 | 293 | 10-20% PEG3350 4% tacsimate |