1H4O
Monoclinic form of human peroxiredoxin 5
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM30A |
Synchrotron site | ESRF |
Beamline | BM30A |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2000-05-15 |
Detector | MAR scanner 345 mm plate |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 130.790, 66.490, 141.240 |
Unit cell angles | 90.00, 117.54, 90.00 |
Refinement procedure
Resolution | 24.000 - 1.950 |
R-factor | 0.166 |
Rwork | 0.165 |
R-free | 0.19000 |
Structure solution method | SIR |
RMSD bond length | 0.018 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MLPHARE |
Refinement software | REFMAC (5.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 24.000 | 2.000 |
High resolution limit [Å] | 1.950 | 1.950 |
Rmerge | 0.032 | 0.142 |
Number of reflections | 151926 | |
<I/σ(I)> | 21 | 5 |
Completeness [%] | 96.6 | 96.6 |
Redundancy | 1.83 | 1.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.3 | PROTEIN WAS CRYSTALLIZED FROM 1.6 M AMMONIUM SULFATE, 0.1 M SODIUM CITRATE BUFFER PH 5.3, 0.2 M POTASSIUM SODIUM TARTRATE, 1 MM DTT, 0.02 % (W/V) SODIUM AZIDE |