5XOV
Crystal structure of peptide-HLA-A24 bound to S19-2 V-delta/V-beta TCR
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | Cu FINE FOCUS |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2008-10-10 |
Detector | RIGAKU RAXIS IV++ |
Wavelength(s) | 1.54180 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 101.992, 73.789, 163.781 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 37.999 - 2.684 |
R-factor | 0.205 |
Rwork | 0.203 |
R-free | 0.24500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1a9e 2ial |
RMSD bond length | 0.005 |
RMSD bond angle | 0.879 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.780 |
High resolution limit [Å] | 2.680 | 2.680 |
Number of reflections | 68358 | |
<I/σ(I)> | 12.8 | 2.1 |
Completeness [%] | 99.8 | 99.8 |
Redundancy | 3.4 | 3.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 288 | 5%(v/v) Tacsimate pH 7.0, 0.1M HEPES, pH 7.3, 10%(w/v) polyethylene glycol monomethyl either 5000 |