5Z2S
Crystal structure of DUX4-HD2 domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-12-16 |
Detector | MAR CCD 130 mm |
Wavelength(s) | 0.9792 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 25.150, 25.390, 72.570 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 23.966 - 1.500 |
R-factor | 0.19 |
Rwork | 0.189 |
R-free | 0.21540 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3a02 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.127 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((1.11.1_2575)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 36.300 | 1.580 |
High resolution limit [Å] | 1.500 | 1.500 |
Number of reflections | 7483 | |
<I/σ(I)> | 19.2 | |
Completeness [%] | 100.0 | |
Redundancy | 6.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 273 | PEG 4000 |