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1V33

Crystal structure of DNA primase from Pyrococcus horikoshii

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL41XU
Synchrotron siteSPring-8
BeamlineBL41XU
Temperature [K]90
Detector technologyCCD
Collection date1999-11-20
DetectorMARRESEARCH
Wavelength(s)1.000
Spacegroup nameP 32 2 1
Unit cell lengths76.451, 76.451, 128.894
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000

*

- 1.800
Rwork0.219
R-free0.24400

*

Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.487
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.830
High resolution limit [Å]1.8001.800
Rmerge0.0480.176
Number of reflections38381
<I/σ(I)>15.24.2
Completeness [%]90.675.8
Redundancy6.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7293PEG 8000, AMMONIUM SULFATE, POTASSIUM PHOSPHATE, SODIUM CACODYLATE, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein6-10 (mg/ml)
21reservoirPEG800010.5 (%)
31reservoirammonium sulfate10 (mM)
41reservoirpotassium phosphate22.5 (mM)pH7
51reservoirsodium phosphate5 (mM)pH6.5

227344

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