6MBI
Crystal Structure of SNX15 PX domain in domain swapped conformation form 2
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 | 2018-08-24 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9796 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 60.312, 60.312, 85.161 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 49.219 - 2.834 |
| R-factor | 0.282 |
| Rwork | 0.278 |
| R-free | 0.31910 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6ecm |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.517 |
| 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] | 49.220 | 2.980 |
| High resolution limit [Å] | 2.830 | 2.830 |
| Rmerge | 0.094 | 0.728 |
| Rpim | 0.028 | 0.210 |
| Number of reflections | 4100 | 565 |
| <I/σ(I)> | 14.4 | 2.6 |
| Completeness [%] | 99.4 | 96.2 |
| Redundancy | 12.2 | 12.6 |
| CC(1/2) | 0.999 | 0.960 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293 | 4 M NaCl, 0.1 Tris (pH 8.5) |






