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9UL7

Improved thermostability of a GH3 glycosidase based on its X-ray crystal structure

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL19U1
Synchrotron siteSSRF
BeamlineBL19U1
Temperature [K]100
Detector technologyPIXEL
Collection date2021-05-24
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.987
Spacegroup nameC 1 2 1
Unit cell lengths112.866, 104.617, 69.156
Unit cell angles90.00, 91.91, 90.00
Refinement procedure
Resolution34.559 - 2.200
R-factor0.1917
Rwork0.190
R-free0.23610
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.007
RMSD bond angle0.920
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((1.14_3260: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.240
High resolution limit [Å]2.2002.200
Number of reflections27364540984
<I/σ(I)>25.643
Completeness [%]99.9
Redundancy6.7
CC(1/2)0.9960.940
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2970.1 M MES pH 6.5 25% (v/v) PEG 550 MME

246031

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