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3I2Q

Crystal structure of the hairpin ribozyme with 2'OMe substrate strand and N1-deazaadenosine at position A9

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]100
Detector technologyCCD
Collection date2009-01-29
DetectorADSC QUANTUM 315r
Wavelength(s)0.9700
Spacegroup nameP 61 2 2
Unit cell lengths93.350, 93.350, 131.450
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution40.420 - 2.900
R-factor0.203
Rwork0.203
R-free0.22700
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)2oue
RMSD bond length0.006
RMSD bond angle1.400
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.900
High resolution limit [Å]2.8002.800
Rmerge0.0770.361
Number of reflections9310
<I/σ(I)>7.71.8
Completeness [%]99.899.8
Redundancy7.87.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7293.15Well solutions contained 20.5% w/v PEG 2000 MME, 0.10 M Na cacodylate, pH 6.5 or 7.0, 0.25 M Li2SO4, 2.5 mM Co(NH3)6Cl3 and 2 mM Spermidine-HCl. Crystals grew as hexagonal rods or plates and reached a size of 0.3 mm x 0.2 mm x 0.2 mm in approximately 3 weeks, VAPOR DIFFUSION, HANGING DROP, temperature 293.15K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
11PEG 2000 MME
101Spermidine-HCl
21Na cacodylate
31Li2SO4
41Co(NH3)6Cl3
51Spermidine-HCl
61PEG 2000 MME
71Na cacodylate
81Li2SO4
91Co(NH3)6Cl3

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PDB entries from 2024-05-15

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