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3NKB

A 1.9A crystal structure of the HDV ribozyme precleavage suggests both Lewis acid and general acid mechanisms contribute to phosphodiester cleavage

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2010-03-15
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.97872
Spacegroup nameC 2 2 21
Unit cell lengths64.837, 84.107, 102.020
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution27.361 - 1.916
R-factor0.2169
Rwork0.214
R-free0.24100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1CX0 WITH PORTIONS OF P2 AND P4 DELETED
RMSD bond length0.003
RMSD bond angle1.254
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX (1.6_289)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.950
High resolution limit [Å]1.9001.900
Number of reflections20583
<I/σ(I)>44.32.2
Completeness [%]94.354.6
Redundancy7.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP52933.5 mg/mL RNA, 10 mM MgCl2, 50 mM potassium acetate, 1 mM spermine, 30% MPD, pH 5.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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