1VSL
ASV INTEGRASE CORE DOMAIN D64N MUTATION WITH ZINC CATION
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | ENRAF-NONIUS FR591 |
| Temperature [K] | 295 |
| Detector technology | IMAGE PLATE |
| Collection date | 1998-01-15 |
| Detector | MACSCIENCE |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 67.159, 67.159, 79.651 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 8.000 - 2.200 |
| R-factor | 0.156 |
| Rwork | 0.156 |
| R-free | 0.24400 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1asv |
| RMSD bond length | 0.015 |
| RMSD bond angle | 25.600 * |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | X-PLOR |
| Refinement software | X-PLOR (3.1) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.260 |
| High resolution limit [Å] | 2.200 | 2.190 |
| Rmerge | 0.068 * | |
| Total number of observations | 33008 * | |
| Number of reflections | 9425 * | |
| <I/σ(I)> | 12.8 | 2.3 |
| Completeness [%] | 96.8 | 98 |
| Redundancy | 3.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 7.5 * | Bujacz, G., (1995) J. Mol. Biol., 253, 333. * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | protein | 6-7.5 (mg/ml) | |
| 2 | 1 | reservoir | HEPES | 100 (mM) | |
| 3 | 1 | reservoir | isopropanol | 10 (%) | |
| 4 | 1 | reservoir | PEG4000 | 20 (%) |






