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3D0P

Insights into RNA/DNA hybrid recognition and processing by RNase H from the crystal structure of a non-specific enzyme-dsDNA complex

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2007-10-21
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.97850
Spacegroup nameC 1 2 1
Unit cell lengths98.397, 66.660, 76.926
Unit cell angles90.00, 122.31, 90.00
Refinement procedure
Resolution41.590 - 1.800
R-factor0.21539
Rwork0.214
R-free0.24108
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1zbi using one protein molecule.
RMSD bond length0.016
RMSD bond angle1.672
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.4.0066)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.860
High resolution limit [Å]1.8001.800
Rmerge0.0610.248
Number of reflections37768
<I/σ(I)>12.412.4
Completeness [%]97.394.7
Redundancy7.77.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.62910.1 M sodium acetate, 8 % (w/v) PEG 4000, pH 4.6, VAPOR DIFFUSION, SITTING DROP, temperature 291K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111sodium acetate
211PEG 4000
312sodium acetate
412PEG 4000

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