7XRF
Crystal structaure of DgpB/C complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 80 |
Detector technology | PIXEL |
Collection date | 2021-05-06 |
Detector | DECTRIS EIGER R 4M |
Wavelength(s) | 0.9875 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 78.076, 159.704, 176.168 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.836 - 2.137 |
R-factor | 0.2069 |
Rwork | 0.206 |
R-free | 0.25100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7exz |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.100 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.200 | 0.860 |
Number of reflections | 226255 | 689 |
<I/σ(I)> | 6.3 | |
Completeness [%] | 99.9 | |
Redundancy | 14.5 | |
CC(1/2) | 0.860 | 0.850 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 0.2 M magnesium acetate and 10% PEG 8000 |