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 |