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1H89

CRYSTAL STRUCTURE OF TERNARY PROTEIN-DNA COMPLEX2

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL45XU
Synchrotron siteSPring-8
BeamlineBL45XU
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-11-17
DetectorRIGAKU RAXIS IV
Spacegroup nameP 21 21 21
Unit cell lengths62.684, 73.383, 161.699
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000

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- 2.450
R-factor0.229
Rwork0.229
R-free0.26700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1h88
RMSD bond length0.005
RMSD bond angle1.120

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.851)
Refinement softwareCNS (0.9)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.540
High resolution limit [Å]2.4502.450
Rmerge0.072

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Total number of observations205777

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Number of reflections27451
<I/σ(I)>27.50432.162
Completeness [%]99.095.5
Redundancy7.4964
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.8

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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)
41reservoir0.1 (M)
51reservoir0.005 (M)
61reservoirsodium HEPES0.05 (M)pH7.0
71reservoirMPD4 (%(v/v))
81reservoirglycerol6 (%(v/v))

227561

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