1H37
Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU RU200B |
| Temperature [K] | 298 |
| Detector technology | AREA DETECTOR |
| Detector | SIEMENS |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 141.217, 141.217, 244.982 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 40.000 * - 2.800 |
| R-factor | 0.205 |
| Rwork | 0.205 |
| R-free | 0.24800 |
| Structure solution method | OTHER |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.200 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Refinement software | CNS (1.1) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 40.000 * |
| High resolution limit [Å] | 2.800 |
| Rmerge | 0.094 |
| Total number of observations | 180971 * |
| Number of reflections | 56400 |
| <I/σ(I)> | 6.8 |
| Completeness [%] | 81.0 * |
| Redundancy | 3.2 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 4.8 | 20 * | pH 4.80 |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | protein | 5-8 (mg/ml) | |
| 2 | 1 | reservoir | sodium citrate | 50 (mM) | pH4.8 |
| 3 | 1 | reservoir | 50 (mM) | ||
| 4 | 1 | reservoir | PEG600 | 3-9 (%(v/v)) | |
| 5 | 1 | reservoir | 0.3 (%(w/v)) |






