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 |






