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1MME

THE CRYSTAL STRUCTURE OF AN ALL-RNA HAMMERHEAD RIBOZYME: A PROPOSED MECHANISM FOR RNA CATALYTIC CLEAVAGE

Experimental procedure
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX9.6
Synchrotron siteSRS
BeamlinePX9.6
Temperature [K]173
Detector technologyIMAGE PLATE
Collection date1994-11-03
DetectorMARRESEARCH
Spacegroup nameP 31 2 1
Unit cell lengths64.980, 64.980, 138.140
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution15.000 - 3.100
R-factor0.251
Rwork0.251
R-free0.29300
RMSD bond length0.010
RMSD bond angle16.500

*

Data reduction softwareIPMOSFLM
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 Overall
Low resolution limit [Å]15.000
High resolution limit [Å]3.100
Rmerge0.085
Number of reflections6529
Completeness [%]99.9
Redundancy3.3

*

Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.520

*

pH 6.50, VAPOR DIFFUSION, SITTING DROP, temperature 293.00K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111WATER
211PEG 6000
311GLYCEROL
411NH4 CACODYLATE
511NH4 ACETATE
611MG ACETATE
711SPERMINE
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropribozyme complex0.5 (mM)
21dropammonium cacodylate10 (mM)
31reservoirammonium cacodylate50 (mM)
41reservoir100 (mM)
51reservoir10 (mM)
61reservoirspermine1 (mM)
71reservoirPEG600023 (%)
81reservoirglycerol5 (%)

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