6XUU
Crystallographic structure of oligosaccharide dehydrogenase from Pycnoporus cinnabarinus, glucose-bound form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ELETTRA BEAMLINE 11.2C |
Synchrotron site | ELETTRA |
Beamline | 11.2C |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-11-14 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 49.137, 61.618, 195.954 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.040 - 1.570 |
R-factor | 0.16358 |
Rwork | 0.162 |
R-free | 0.18889 |
Structure solution method | FOURIER SYNTHESIS |
RMSD bond length | 0.013 |
RMSD bond angle | 1.856 |
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] | 49.040 | 1.670 |
High resolution limit [Å] | 1.570 | 1.570 |
Number of reflections | 103996 | 29033 |
<I/σ(I)> | 12 | |
Completeness [%] | 99.6 | |
Redundancy | 6.6 | |
CC(1/2) | 0.990 | 0.560 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 294 | 2 M ammonium sulfate |