8EB9
Crystal structure of SIX8 from Fusarium oxysporum f. sp. lycopersici
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-08-09 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.95373 |
| Spacegroup name | P 43 2 2 |
| Unit cell lengths | 51.814, 51.814, 81.599 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 36.640 - 1.280 |
| R-factor | 0.1715 |
| Rwork | 0.170 |
| R-free | 0.19330 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | SIX8 alphafold model |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.210 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.640 | 1.326 |
| High resolution limit [Å] | 1.280 | 1.280 |
| Rmerge | 0.048 | 1.350 |
| Rmeas | 0.050 | 1.405 |
| Rpim | 0.014 | |
| Number of reflections | 29449 | 2869 |
| <I/σ(I)> | 23.71 | |
| Completeness [%] | 100.0 | 99.1 |
| Redundancy | 13 | |
| CC(1/2) | 0.999 | 0.725 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.17 M Ammonium sulfate, 15% glycerol, 25.5% PEG4000 |






