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6QUK

Protein crystallization by ionic liquid hydrogel support: glucose isomerase grown by using ionic liquid hydrogel

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]100
Detector technologyPIXEL
Collection date2016-12-12
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.97779
Spacegroup nameP 21 21 2
Unit cell lengths85.900, 92.598, 99.111
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution62.980 - 1.580
R-factor0.16824
Rwork0.167
R-free0.19449
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1oad
RMSD bond length0.008
RMSD bond angle0.635
Data reduction softwarexia2
Data scaling softwareAimless
Phasing softwareSir2014
Refinement softwareREFMAC (5.8.0238)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]64.9001.620
High resolution limit [Å]1.5801.580
Rmerge0.0990.664
Rmeas0.1150.791
Rpim0.0700.492
Number of reflections1033567748
<I/σ(I)>11.13.4
Completeness [%]95.697.4
Redundancy4.24.1
CC(1/2)0.9950.622
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION7298protein 26mg/m in HEPES 10mM pH 7 and MgCl2 1mM Reservoir: (NH4)2SO4 1.5M

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