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2PL4

D-(GGTATACC) under 0.55 GPa hydrostatic pressure

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID27
Synchrotron siteESRF
BeamlineID27
Temperature [K]295
Detector technologyIMAGE PLATE
Collection date2006-11-10
DetectorMAR scanner 345 mm plate
Wavelength(s)0.3738
Spacegroup nameP 61
Unit cell lengths43.710, 43.710, 40.710
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution10.000 - 1.650
R-factor0.1693
Rwork0.168
R-free0.20100
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)2pkv
RMSD bond length0.010
RMSD bond angle0.028
Data reduction softwareXDS
Data scaling softwareSCALA
Refinement softwareSHELXL-97
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]18.0001.750
High resolution limit [Å]1.6501.650
Rmerge0.0430.188
Number of reflections5057
<I/σ(I)>10.23.6
Completeness [%]94.186.2
Redundancy3.22.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP729010 mg of octamer dissolved in cacodylate buffer (10-2 M, 15 % MPD) additives : 10-5 M sodium azide, 10-2 M MgCl2, 2.10-2 M spermine chloride. Reservoir: same solution but 50 % MPD, pH 7, VAPOR DIFFUSION, SITTING DROP, temperature 290K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111cacodylate buffer
1012spermine chloride
211MPD
311sodium azide
411MgCl2
511spermine chloride
612cacodylate buffer
712MPD
812sodium azide
912MgCl2

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