3GX0
Crystal Structure of GSH-dependent Disulfide bond Oxidoreductase
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | BRUKER AXS MICROSTAR |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2007-01-01 |
| Detector | Bruker Platinum 135 |
| Wavelength(s) | 1.5418 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 68.490, 68.490, 111.990 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 20.000 - 2.300 |
| R-factor | 0.1935 |
| Rwork | 0.191 |
| R-free | 0.24981 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.017 |
| RMSD bond angle | 1.662 |
| Data reduction software | SAINT |
| Data scaling software | SAINT |
| Phasing software | PHASER |
| Refinement software | REFMAC |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.400 |
| High resolution limit [Å] | 2.300 | 2.300 |
| Rmerge | 0.130 | 0.551 |
| Number of reflections | 12571 | |
| <I/σ(I)> | 17.5 | 3.35 |
| Completeness [%] | 99.8 | 98.5 |
| Redundancy | 10.9 | 6.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | Protein in 20 mM potassium dihydrogen phosphate, 2 mM DTT, 1mM EDTA, 10 mM glutathione. Well solution: 20% w/v PEG 3000, 100 mM acetate., VAPOR DIFFUSION, HANGING DROP |






