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1E73

2-F-glucosylated MYROSINASE FROM SINAPIS ALBA with bound L-ascorbate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-3
Synchrotron siteESRF
BeamlineID14-3
Temperature [K]100
Detector technologyCCD
Collection date1997-10-15
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths135.300, 137.200, 80.600
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 1.500
R-factor0.134

*

Rwork0.134
R-free0.16700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1e4m
RMSD bond length0.021
RMSD bond angle0.036
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareX-PLOR
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]34.7001.580
High resolution limit [Å]1.5001.500
Rmerge0.0630.352
Number of reflections98776
<I/σ(I)>82.1
Completeness [%]82.771.4
Redundancy4.23.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.5

*

Burmeister, W.P., (1997) Structure (London), 5, 663.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropmyrosinase12 (mg/ml)
21dropHEPES30 (mM)
31drop0.05 (%)
41reservoirammonium sulfate66 (%sat)
51reservoirTris-HCl100 (mM)

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