5FQ9
Crystal structure of the OXA10 with 1C
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04 |
| Synchrotron site | Diamond |
| Beamline | I04 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2015-09-27 |
| Detector | DECTRIS PILATUS 6M |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 48.898, 103.109, 125.529 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 15.424 - 1.500 |
| R-factor | 0.158 |
| Rwork | 0.157 |
| R-free | 0.18060 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1k6r |
| RMSD bond length | 0.014 |
| RMSD bond angle | 1.344 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | PHENIX |
| Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 15.440 | 1.120 |
| High resolution limit [Å] | 1.500 | 1.100 |
| Rmerge | 0.050 | 1.100 |
| Number of reflections | 253261 | |
| <I/σ(I)> | 5.6 | 2 |
| Completeness [%] | 99.9 | 99.5 |
| Redundancy | 5.9 | 8.9 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 5.5 | 0.2M NACL, 0.1M NA ACETATE PH 5.0, 20% PEG 6000 |






