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1OPO

THE STRUCTURE OF CARNATION MOTTLE VIRUS

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date1990-07-15
DetectorHENDRIX-LENTFER
Wavelength(s)0.96
Spacegroup nameI 2 3
Unit cell lengths382.600, 382.600, 382.600
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution6.000 - 3.200
R-factor0.183
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2tbv
RMSD bond length0.021
RMSD bond angle4.150
Data scaling softwareSCALEPACK
Phasing softwareGAP ((OXFORD))
Refinement softwareX-PLOR (2.1)
Data quality characteristics
 Overall
Low resolution limit [Å]6.000
High resolution limit [Å]3.200
Rmerge0.082
Number of reflections140483
Completeness [%]91.0
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5.032980.1M Tris-maleic (mal)/NaOH, 25% saturated ammonium sulphate, 1.7-heptandiol or PEG 300 were added to lessen the number of pellets, pH 5.03, VAPOR DIFFUSION, SITTING DROP, temperature 298.0K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropTris-HCl0.1 (M)
21dropvirus40-50 (mg/ml)
31dropammonium sulfate10 (%sat)
41reservoirTris-maleic/NaOH0.1 (M)pH5.03
51reservoirammonium sulfate25 (%sat)

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