4A9Z
CRYSTAL STRUCTURE OF HUMAN P63 TETRAMERIZATION DOMAIN
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I02 |
| Synchrotron site | Diamond |
| Beamline | I02 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2011-10-21 |
| Detector | ADSC CCD |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 80.850, 80.850, 68.370 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 48.920 - 2.290 |
| R-factor | 0.1967 |
| Rwork | 0.194 |
| R-free | 0.24590 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.010 |
| RMSD bond angle | 0.980 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | BUSTER (2.10.0) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 70.020 | 2.410 |
| High resolution limit [Å] | 2.290 | 2.290 |
| Rmerge | 0.050 | 0.980 |
| Number of reflections | 11980 | |
| <I/σ(I)> | 15.7 | 2.1 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 10.2 | 8.3 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 |






