6PX6
HLA-TCR 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 | CCD |
Collection date | 2019-05-11 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.953728973866 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 72.534, 99.416, 72.565 |
Unit cell angles | 90.00, 118.26, 90.00 |
Refinement procedure
Resolution | 39.238 - 3.000 |
R-factor | 0.207648302688 |
Rwork | 0.205 |
R-free | 0.25702 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4ozh |
RMSD bond length | 0.002 |
RMSD bond angle | 0.595 |
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] | 39.240 | 3.180 |
High resolution limit [Å] | 3.000 | 3.000 |
Number of reflections | 18263 | 18263 |
<I/σ(I)> | 4.21 | |
Completeness [%] | 99.9 | |
Redundancy | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 294 | 0.1 M MOPS/HEPES, pH 7.5, 12.5% v/v PEG1000, 12.5% v/v MPD, 12.5% w/v PEG3350, 0.04 M NPS mixture |