6B4K
Crystal structure of human DDX19B(AMPPNP)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-D |
| Synchrotron site | APS |
| Beamline | 23-ID-D |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-12-11 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.0332 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 83.233, 45.364, 127.391 |
| Unit cell angles | 90.00, 97.03, 90.00 |
Refinement procedure
| Resolution | 42.144 - 2.200 |
| R-factor | 0.2086 |
| Rwork | 0.207 |
| R-free | 0.24840 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3ews |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.623 |
| Data reduction software | DIALS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.300 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rpim | 0.053 | 0.979 |
| Number of reflections | 48313 | 4099 |
| <I/σ(I)> | 10 | 1.7 |
| Completeness [%] | 99.4 | 97.9 |
| Redundancy | 6.9 | 6.1 |
| CC(1/2) | 0.994 | 0.452 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 277 | 0.1 M MIB buffer pH 5.0 (malonate, imidazole, borate), 13 % (w/v) PEG 1500 |






