3VFP
crystal structure of HLA B*3508 LPEP158G, HLA mutant Gly158
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 | 2011-04-08 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 0.9536 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 50.993, 81.505, 110.899 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.481 - 1.850 |
R-factor | 0.2104 |
Rwork | 0.207 |
R-free | 0.26590 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1zhk |
RMSD bond length | 0.007 |
RMSD bond angle | 1.004 |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.7.1_743) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 1.800 | |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.079 | 0.198 |
Number of reflections | 3328 | |
<I/σ(I)> | 16.55 | 8.12 |
Completeness [%] | 70.4 | 41.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 293 | 0.2M ammonium acetate, 16% PEG 4K, 0.1M sodium citrate pH5.6, vapor diffusion, hanging drop, temperature 293K |