1GH2
Crystal structure of the catalytic domain of a new human thioredoxin-like protein
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU RU200 |
| Temperature [K] | 115 |
| Detector technology | IMAGE PLATE |
| Collection date | 2000-08-28 |
| Detector | MAR scanner 345 mm plate |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 87.500, 48.500, 29.800 |
| Unit cell angles | 90.00, 99.59, 90.00 |
Refinement procedure
| Resolution | 15.000 - 2.220 |
| Rwork | 0.221 |
| R-free | 0.25300 |
| RMSD bond length | 0.020 * |
| RMSD bond angle | 1.970 * |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | AMoRE |
| Refinement software | CNS (0.9) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 100.000 | 2.300 |
| High resolution limit [Å] | 2.220 | 2.220 |
| Rmerge | 0.089 | 0.316 |
| Number of reflections | 6710 * | 624 * |
| <I/σ(I)> | 8.4 | |
| Completeness [%] | 99.8 * | 98.7 |
| Redundancy | 7.2 | 6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 5 | 291 | ammonium sulfate, pH 5.0, EVAPORATION, temperature 291.0K |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | reservoir | ammonium sulfate |






