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1B35

CRICKET PARALYSIS VIRUS (CRPV)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE F1
Synchrotron siteCHESS
BeamlineF1
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-07-07
DetectorFUJI
Spacegroup nameI 2 2 2
Unit cell lengths330.000, 334.000, 395.000
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution15.000 - 2.400
R-factor0.228
Rwork0.228
R-free0.24200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2plv
RMSD bond length0.007
RMSD bond angle1.400
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Refinement softwareCNS (0.4)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.440
High resolution limit [Å]2.4002.400
Rmerge0.128

*

0.015
Total number of observations312272

*

Number of reflections210945
<I/σ(I)>115
Completeness [%]25.29.2
Redundancy1.231.06
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.2

*

VIRUS STORED AT 10MG/ML IN 200MM NAH2PO4, PH7.2. WELL SOLUTION CONSISTED OF 8% (W/V) MPEG 5K, 50MM LI2SO4, 50MM MES, PH6.0.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropvirus10 (mg/ml)
21dropsodium phosphate200 (mM)
31reservoirmPEG50008 (%(w/v))
41reservoir50 (mM)
51reservoirMES50 (mM)

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