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1BX3

EFFECTS OF COMMONLY USED CRYOPROTECTANTS ON GLYCOGEN PHOSPHORYLASE ACTIVITY AND STRUCTURE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-07-29
DetectorMARRESEARCH
Spacegroup nameP 43 21 2
Unit cell lengths126.040, 126.040, 115.190
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution36.800 - 2.300
R-factor0.186
Rwork0.186
R-free0.25200
Structure solution methodOTHER
Starting model (for MR)2gpn
RMSD bond length0.009
RMSD bond angle1.200
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCCP4
Refinement softwareX-PLOR (3.8)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]36.8002.340
High resolution limit [Å]2.3002.300
Rmerge0.0420.103
Total number of observations244996

*

Number of reflections41713
<I/σ(I)>20.5910.48
Completeness [%]99.999.5
Redundancy5.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1unknown

*

6.716

*

Oikonomakos, N.G., (1985) Biochim.Biophys.Acta., 832, 248.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111phosphorylase b27.5 (mg/ml)
211IMP1.1 (mM)
311spermine1.1 (mM)
411Bes10 (mM)
511dithiothreitol2.9 (mM)
611EDTA0.1 (mM)

249697

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