6TIV
Crystal structure of the SVS_A2 protein (205-DREMH-209 /205-AQDLE-209 mutant) from ancestral sequence reconstruction at 2.38 A resolution
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | MAX IV BEAMLINE BioMAX |
| Synchrotron site | MAX IV |
| Beamline | BioMAX |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-06-28 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.91842 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 74.079, 104.250, 108.189 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 29.000 - 2.380 |
| R-factor | 0.1877 |
| Rwork | 0.186 |
| R-free | 0.21030 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4okz |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.698 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0253) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 29.660 | 2.480 |
| High resolution limit [Å] | 2.380 | 2.380 |
| Rmerge | 0.129 | 0.526 |
| Rpim | 0.057 | 0.234 |
| Number of reflections | 34458 | 4109 |
| <I/σ(I)> | 7.7 | 3 |
| Completeness [%] | 99.8 | 98.8 |
| Redundancy | 6.7 | |
| CC(1/2) | 0.994 | 0.855 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 293 | 0.2M Na phosphate 0.1M Bis-Tris-Propane pH 6.5 20% PEG 3350 |






