1OGA
A structural basis for immunodominant human T-cell receptor recognition.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2002-08-15 |
Detector | ADSC CCD |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 67.019, 108.838, 77.741 |
Unit cell angles | 90.00, 112.46, 90.00 |
Refinement procedure
Resolution | 30.000 * - 1.400 |
R-factor | 0.218 |
Rwork | 0.218 |
R-free | 0.23200 * |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1qsf |
RMSD bond length | 0.008 |
RMSD bond angle | 25.600 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | EPMR |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.450 |
High resolution limit [Å] | 1.400 | 1.400 |
Rmerge | 0.063 | 0.830 |
Total number of observations | 3465000 * | |
Number of reflections | 200813 | |
<I/σ(I)> | 38.5 | 1.9 |
Completeness [%] | 99.4 | 98.3 |
Redundancy | 17.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 6.5 | 14% PEG8000, 50MM MES PH 6.5 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | PEG8000 | 14 (%) | |
3 | 1 | drop | MES | 50 (mM) | pH6.5 |