8F6D
Crystal structure of the CNNM2 CBS-pair domain in complex with ARL15
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-E |
| Synchrotron site | APS |
| Beamline | 24-ID-E |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-04-14 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.97918 |
| Spacegroup name | P 1 |
| Unit cell lengths | 66.018, 73.323, 79.327 |
| Unit cell angles | 94.35, 95.50, 115.33 |
Refinement procedure
| Resolution | 29.530 - 3.200 |
| R-factor | 0.2655 |
| Rwork | 0.264 |
| R-free | 0.29270 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4iy0 |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.791 |
| Data reduction software | DIALS |
| Data scaling software | DIALS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.19_4092) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 3.260 |
| High resolution limit [Å] | 3.200 | 3.200 |
| Number of reflections | 20526 | 1986 |
| <I/σ(I)> | 10.4 | 0.6 |
| Completeness [%] | 94.2 | 93.1 |
| Redundancy | 3.7 | 3.8 |
| CC(1/2) | 0.998 | 0.624 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 294 | 0.2 M sodium chloride, 0.1 M Tris pH 8.5, 25% (w/v) PEG3350, 0.5 mM GppNp |






