6ECM
Crystal Structure of SNX15 PX domain in domain swapped conformation
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 | 2018-08-01 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9796 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 54.498, 54.498, 83.580 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.000 - 2.353 |
| R-factor | 0.2499 |
| Rwork | 0.244 |
| R-free | 0.29890 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4ikd |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.036 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.000 | 2.430 |
| High resolution limit [Å] | 2.350 | 2.350 |
| Rmerge | 0.076 | 1.074 |
| Rpim | 0.015 | 0.216 |
| Number of reflections | 5645 | 505 |
| <I/σ(I)> | 20.9 | 3.1 |
| Completeness [%] | 99.4 | 94.3 |
| Redundancy | 26.2 | 24.6 |
| CC(1/2) | 1.000 | 0.982 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293 | 0.1 M Tris (pH 8.5) 200 mM LiSO4, 24% PEG4000, 10% glycerol |






