5HR0
Crystal structure of thioredoxin E101G mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-07-08 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.9191 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 50.043, 50.043, 163.291 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.862 - 1.310 |
R-factor | 0.1757 |
Rwork | 0.174 |
R-free | 0.20920 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2trx |
RMSD bond length | 0.011 |
RMSD bond angle | 1.095 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (dev_2247) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 19.862 | 50.000 | 1.360 |
High resolution limit [Å] | 1.310 | 2.820 | 1.310 |
Rmerge | 0.055 | 0.038 | 0.451 |
Total number of observations | 588774 | ||
Number of reflections | 57845 | ||
<I/σ(I)> | 17 | ||
Completeness [%] | 99.6 | 96.1 | 99.9 |
Redundancy | 5.4 | 5.5 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | The drop was a 1:1 mix of protein (18 mg/ml in water) and reservoir solution (100 mM sodium acetate, 4 mM CuSO4, 15 % ethanol, pH 4.75) |