5A9P
Crystal structure of Operophtera brumata CPV18 polyhedra
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I24 |
| Synchrotron site | Diamond |
| Beamline | I24 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Detector | DECTRIS PILATUS 6M |
| Spacegroup name | I 2 3 |
| Unit cell lengths | 102.770, 102.770, 102.770 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 72.669 - 1.476 |
| R-factor | 0.1311 |
| Rwork | 0.130 |
| R-free | 0.14750 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2oh6 |
| RMSD bond length | 0.005 |
| RMSD bond angle | 1.146 |
| Data reduction software | xia2 |
| Data scaling software | xia2 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 72.700 | 1.510 |
| High resolution limit [Å] | 1.480 | 1.480 |
| Rmerge | 0.320 | |
| Number of reflections | 30415 | |
| <I/σ(I)> | 7.1 | 1.5 |
| Completeness [%] | 100.0 | 99.8 |
| Redundancy | 12.9 | 8.6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 7.5 | PH 7.5 |






