1R5A
Glutathione S-transferase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2001-10-01 |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 1.5418 |
Spacegroup name | I 41 2 2 |
Unit cell lengths | 122.129, 122.129, 74.699 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.500 |
Rwork | 0.233 |
R-free | 0.26500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1v2a |
RMSD bond length | 0.007 |
RMSD bond angle | 20.800 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.078 | 0.396 |
Total number of observations | 37582 * | |
Number of reflections | 9605 | 963 * |
<I/σ(I)> | 12.9 | 2.6 |
Completeness [%] | 95.6 | 97.9 |
Redundancy | 3.9 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 298 | 1.75M lithium sulfate, 0.1M potassium phosphate, 1mM Copper (II) chloride, 10mM glutathione-sulfonic acid, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298.0K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | 1.6-2 (M) | ||
2 | 1 | reservoir | 1 (mM) | ||
3 | 1 | reservoir | sodium phosphate | 100 (mM) | pH6.5-7.5 |
4 | 1 | drop | protein | 13.1 (mg/ml) | |
5 | 1 | drop | glutathione sulphonic acid | 10 (mM) |