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379D

THE STRUCTURAL BASIS OF HAMMERHEAD RIBOZYME SELF-CLEAVAGE

Experimental procedure
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X12C
Synchrotron siteNSLS
BeamlineX12C
Temperature [K]100
Detector technologyCCD
Collection date1997-05-09
DetectorCUSTOM-MADE
Spacegroup nameP 31 2 1
Unit cell lengths65.100, 65.100, 138.700
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution8.000 - 3.100
R-factor0.23
Rwork0.230
R-free0.28000

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Structure solution methodPHASED FROM ISOMORPHOUS CRYSTAL
Starting model (for MR)HAMMERHEAD RIBOZYME "GROUND STATE" AT PH 6.
RMSD bond length0.009
RMSD bond angle18.900

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.8)
Refinement softwareX-PLOR
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0003.270
High resolution limit [Å]3.1003.100
Rmerge0.0460.123
Number of reflections6203
<I/σ(I)>12.65.8
Completeness [%]91.675.1

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Redundancy2.12.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1unknown

*

6

*

pH 8.50, VAPOR DIFFUSION, SITTING DROP
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111WATER
211LI SULFATE
311NA CACODYLATE
411EDTA
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11RNA1 (mM)
2121.8 (M)
312sodium cacodylate50 (mM)
4121.5 (mM)

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PDB entries from 2024-05-22

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