6Z9G
Structure of [NiFeSe] hydrogenase G491A variant from Desulfovibrio vulgaris Hildenborough pressurized with Oxygen gas - structure G491A-O2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID30B |
| Synchrotron site | ESRF |
| Beamline | ID30B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-09-27 |
| Detector | DECTRIS EIGER X 4M |
| Wavelength(s) | 0.9677 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 120.306, 93.815, 126.951 |
| Unit cell angles | 90.00, 105.20, 90.00 |
Refinement procedure
| Resolution | 61.200 - 1.760 |
| R-factor | 0.1944 |
| Rwork | 0.192 |
| R-free | 0.23970 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5jsk |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.946 |
| Data reduction software | XDS |
| Data scaling software | STARANISO |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 74.480 | 1.930 |
| High resolution limit [Å] | 1.760 | 1.760 |
| Rmerge | 0.114 | 0.814 |
| Rpim | 0.060 | 0.459 |
| Number of reflections | 189459 | 8187 |
| <I/σ(I)> | 7.4 | 1.6 |
| Completeness [%] | 70.4 | 12.7 |
| Redundancy | 4.5 | 3.9 |
| CC(1/2) | 0.997 | 0.676 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.6 | 293 | 20% PEG 1500 (w/v) and 0.1 mM Tris-HCl pH 7.6 |






