1C8I
BINDING MODE OF HYDROXYLAMINE TO ARTHROMYCES RAMOSUS PEROXIDASE
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU RU200 |
| Temperature [K] | 293 |
| Detector technology | IMAGE PLATE |
| Collection date | 1998-08-15 |
| Detector | FUJI |
| Spacegroup name | P 42 21 2 |
| Unit cell lengths | 74.400, 74.400, 117.500 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 7.000 - 2.000 |
| R-factor | 0.162 |
| Rwork | 0.162 |
| R-free | 0.22300 |
| Structure solution method | OTHER |
| Starting model (for MR) | 1gzb |
| RMSD bond length | 0.018 |
| RMSD bond angle | 0.050 |
| Data reduction software | PROCESS |
| Data scaling software | PROCESS |
| Phasing software | X-PLOR |
| Refinement software | X-PLOR |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.250 |
| High resolution limit [Å] | 2.000 | 2.000 |
| Rmerge | 0.068 | 0.177 |
| Total number of observations | 108471 * | |
| Number of reflections | 21938 | |
| Completeness [%] | 94.2 | 90.6 |
| Redundancy | 4.94 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 7.5 * | 22-24 * | used seeding, Kunishima, N., (1993) Proteins: Struct., Funct., Genet., 15, 216. * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | ARP | 20-40 (mg/ml) | |
| 2 | 1 | reservoir | ammonium sulfate | 32 (%sat) | |
| 3 | 1 | reservoir | Tris-HCl | 20 (mM) |






