6XUV
Crystallographic structure of oligosaccharide dehydrogenase from Pycnoporus cinnabarinus, laminaribiose-bound form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I24 |
Synchrotron site | Diamond |
Beamline | I24 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-06-28 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9685 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.914, 60.929, 194.286 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 97.330 - 1.750 |
R-factor | 0.16977 |
Rwork | 0.168 |
R-free | 0.20729 |
Structure solution method | FOURIER SYNTHESIS |
RMSD bond length | 0.014 |
RMSD bond angle | 2.005 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | REFMAC |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 97.330 | 2.020 |
High resolution limit [Å] | 1.750 | 1.750 |
Number of reflections | 59350 | 20470 |
<I/σ(I)> | 7 | |
Completeness [%] | 99.9 | |
Redundancy | 13 | |
CC(1/2) | 0.990 | 0.810 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 294 | 2 M ammonium sulfate |