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464D

DISORDER AND TWIN REFINEMENT OF RNA HEPTAMER DOUBLE HELIX

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM14
Synchrotron siteESRF
BeamlineBM14
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-09-23
DetectorMARRESEARCH
Spacegroup nameP 1
Unit cell lengths26.375, 28.995, 28.995
Unit cell angles110.37, 96.62, 96.62
Refinement procedure
Resolution15.000 - 1.230
R-factor0.127

*

Rwork0.127
R-free0.19330
RMSD bond length0.029
RMSD bond angle0.018
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Refinement softwareSHELXL-97
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]15.0001.240
High resolution limit [Å]1.2301.230
Rmerge0.0500.308
Total number of observations64180

*

Number of reflections18837

*

Completeness [%]82.832.1
Redundancy3.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP62930.5 MM RNA DUPLEX, 12 MM SPERMINE, 40 MM NA-CACODYLATE PH 6.0, 80 MM SRCL2,40 MM LICL, 10 % (V/V) MPD AGAINST 0.5 ML 35 % (V/V) MPD, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111SPERMINE
211SODIUM CACODYLATE
311SRCL2
411LICL
511MPD
612MPD
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein0.5 (mM)
21reservoirsodium cacodylate40 (mM)
31reservoirspermine tetra-HCl12 (mM)
41reservoir80 (mM)
51reservoir40 (mM)
61reservoir10 (%(v/v))

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PDB entries from 2024-12-25

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