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1DUH

CRYSTAL STRUCTURE OF THE CONSERVED DOMAIN IV OF E. COLI 4.5S RNA

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsELETTRA BEAMLINE 5.2R
Synchrotron siteELETTRA
Beamline5.2R
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-08-01
DetectorMARRESEARCH
Wavelength(s)1.0302, 1.3366, 1.3369, 0.9968, 1.3359
Spacegroup nameP 32 2 1
Unit cell lengths69.697, 69.697, 84.102
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution22.500 - 2.700
R-factor0.244
Rwork0.230
R-free0.24500
Structure solution methodMAD
RMSD bond length0.006
RMSD bond angle1.000
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]22.5002.800
High resolution limit [Å]2.7002.700
Rmerge0.0760.593
Total number of observations154595

*

Number of reflections12371
<I/σ(I)>14.52.1
Completeness [%]98.5100
Redundancy4.24.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6303.15CRYSTALLIZED FROM 1.60-1.90 M (NH4)2SO4, 0.09 M MAGNESIUM ACETATE, 0.05 M SODIUM CACODYLATE PH 6.0, AT 303 K. CRYSTALS WERE STABILISED AT 292 K IN A SOLUTION OF 2.20 M (NH4)2SO4, 0.01 M MGCL2, 0.05 M BIS-TRIS-HCL PH 6.0. SOAK CONDITIONS: CRYSTALS WERE SOAKED IN STABILISATION SOLUTION CONTAINING 0.002 M LUTETIUM CHLORIDE HEXAHYDRATE. CRYOPROTECTION CONDITIONS: AFTER ADDITION OF 20% GLYCEROL (W/V) TO THE SOAK SOLUTION, CRYSTALS WERE FLASH-FROZEN IN LIQUID NITROGEN., VAPOR DIFFUSION, SITTING DROP, temperature 303.15K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111MAGNESIUM ACETATE
211SODIUM CACODYLATE
311BIS-TRIS-HCL
411(NH4)2SO4
511MGCL2
611LUCL3
712(NH4)2SO4
812BIS-TRIS-HCL
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirammonium sulfate1.6-1.8 (M)
21reservoir90 (mM)
31reservoirNa cacodylate50 (mM)
41reservoir2 (mM)

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PDB entries from 2024-05-15

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