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1H8A

CRYSTAL STRUCTURE OF TERNARY PROTEIN-DNA COMPLEX3

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL45XU
Synchrotron siteSPring-8
BeamlineBL45XU
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-04-29
DetectorRIGAKU RAXIS IV
Spacegroup nameP 21 21 2
Unit cell lengths109.860, 166.700, 39.600
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000

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- 2.230
R-factor0.245
Rwork0.245
R-free0.28800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1h88
RMSD bond length0.005
RMSD bond angle1.070

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS (0.9)
Refinement softwareCNS (0.9)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.170
High resolution limit [Å]2.1002.100
Rmerge0.069

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Total number of observations162864

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Number of reflections42104
<I/σ(I)>23.94951.784
Completeness [%]97.394.2
Redundancy3.8682.56
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.8

*

297Tahirov, T.H., (2001) Acta Crystallogr.,Sect.D, 57, 1655.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropdithiothreitol10 (mM)pH6.8
21dropDNA10 (%)excess
31dropprotein6.5-7.5 (mg/ml)
41reservoir0.04 (M)
51reservoirsodium cacodylate0.05 (M)pH6.0
61reservoirMPD20 (%(v/v))

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