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1H88

CRYSTAL STRUCTURE OF TERNARY PROTEIN-DNA COMPLEX1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL45XU
Synchrotron siteSPring-8
BeamlineBL45XU
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-02-25
DetectorRIGAKU RAXIS IV
Spacegroup nameP 1 21 1
Unit cell lengths41.735, 156.966, 55.868
Unit cell angles90.00, 100.16, 90.00
Refinement procedure
Resolution20.000

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- 2.800
R-factor0.222
Rwork0.222
R-free0.27700
Structure solution methodMAD AND MIR
RMSD bond length0.006
RMSD bond angle1.140

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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]20.0002.800
High resolution limit [Å]2.7002.700
Rmerge0.046

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Total number of observations56631

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Number of reflections18605
<I/σ(I)>25.25642.109
Completeness [%]96.087.8
Redundancy3.1512.2
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)
41reservoirammonium acetate0.05 (M)
51reservoir0.01 (M)
61reservoirTris-HCl0.05 (M)pH7.5
71reservoirMPD10 (%(v/v))
81reservoirglycerol6 (%(v/v))

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