5EOA
Crystal structure of OPTN E50K mutant and TBK1 complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U |
| Synchrotron site | SSRF |
| Beamline | BL17U |
| Temperature [K] | 291.15 |
| Detector technology | CCD |
| Collection date | 2015-07-25 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.9791 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 36.824, 54.549, 153.305 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 44.444 - 2.503 |
| R-factor | 0.2018 |
| Rwork | 0.199 |
| R-free | 0.26680 |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.896 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.8.2_1309) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 50.000 |
| High resolution limit [Å] | 2.500 |
| Number of reflections | 11226 |
| <I/σ(I)> | 10.42 |
| Completeness [%] | 99.7 |
| Redundancy | 3.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 6 | 291.5 | 0.1M MES monohydrate pH 6.0, 14% w/V Polyethylene glycol 4000 |






