7OK7
Crystal structure of the UNC119B ARL3 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04-1 |
Synchrotron site | Diamond |
Beamline | I04-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-06-24 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.91587 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 110.270, 152.190, 171.840 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 74.820 - 3.150 |
R-factor | 0.2239 |
Rwork | 0.221 |
R-free | 0.26990 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4goj |
RMSD bond length | 0.003 |
RMSD bond angle | 0.712 |
Data reduction software | DIALS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.15.2_3472: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 74.820 | 3.230 |
High resolution limit [Å] | 3.150 | 3.150 |
Number of reflections | 50733 | 3702 |
<I/σ(I)> | 0.114 | |
Completeness [%] | 99.9 | |
Redundancy | 6.7 | |
CC(1/2) | 0.998 | 0.782 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 279 | 1.00 M Ammonium di-hydrogen phosphate, 0.1M Tris PH7.5 |