5OC5
Crystal structure of human tRNA-dihydrouridine(20) synthase dsRBD K419A-K420A mutant
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SOLEIL BEAMLINE PROXIMA 2 |
| Synchrotron site | SOLEIL |
| Beamline | PROXIMA 2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-02-05 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 0.98011 |
| Spacegroup name | P 41 |
| Unit cell lengths | 36.170, 36.170, 75.090 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 36.170 - 1.893 |
| R-factor | 0.1747 |
| Rwork | 0.169 |
| R-free | 0.22620 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4wft |
| RMSD bond length | 0.015 |
| RMSD bond angle | 1.138 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.170 | 1.961 |
| High resolution limit [Å] | 1.893 | 1.893 |
| Rmerge | 0.099 | |
| Number of reflections | 7680 | 710 |
| <I/σ(I)> | 13.3 | 1.29 |
| Completeness [%] | 99.5 | 96.33 |
| Redundancy | 9.4 | 7.7 |
| CC(1/2) | 0.998 | 0.468 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 292 | 35% PEG 4K 1 M LiCl 100 mM Tris |






