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5GR6

Crystal structure of branching enzyme Y500A/D501A double mutant from Cyanothece sp. ATCC 51142

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPHOTON FACTORY BEAMLINE AR-NW12A
Synchrotron sitePhoton Factory
BeamlineAR-NW12A
Temperature [K]100
Detector technologyCCD
Collection date2014-11-22
DetectorADSC QUANTUM 210
Wavelength(s)1.0
Spacegroup nameP 41 21 2
Unit cell lengths133.596, 133.596, 184.227
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution46.060 - 2.000
R-factor0.16319
Rwork0.162
R-free0.19363
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5gqz
RMSD bond length0.024
RMSD bond angle2.056
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0049)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.030
High resolution limit [Å]2.0002.000
Rmerge0.0350.264
Number of reflections112602
<I/σ(I)>60.910.7
Completeness [%]100.0100
Redundancy14.414.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5293magnesium chloride, ethanol, HEPES-NaOH

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