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6XUT

Crystallographic structure of oligosaccharide dehydrogenase from Pycnoporus cinnabarinus, ligand-free form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I24
Synchrotron siteDiamond
BeamlineI24
Temperature [K]100
Detector technologyPIXEL
Collection date2019-06-28
DetectorDECTRIS PILATUS3 6M
Wavelength(s)1
Spacegroup nameP 21 21 21
Unit cell lengths48.874, 61.592, 195.091
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution97.550 - 1.600
R-factor0.16626
Rwork0.165
R-free0.19648
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4ynt
RMSD bond length0.013
RMSD bond angle1.713
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0258)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]97.7401.570
High resolution limit [Å]1.4301.430
Number of reflections10324825836
<I/σ(I)>14.51.72
Completeness [%]99.9
Redundancy12.7
CC(1/2)1.0000.790
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2942 M ammonium sulfate

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