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1PVO

X-ray crystal structure of Rho transcription termination factor in complex with ssRNA substrate and ANPPNP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.3.1
Synchrotron siteALS
Beamline8.3.1
Temperature [K]95
Detector technologyCCD
Collection date2003-01-19
DetectorADSC QUANTUM 4
Wavelength(s)1.00
Spacegroup nameC 1 2 1
Unit cell lengths119.249, 204.649, 147.788
Unit cell angles90.00, 96.54, 90.00
Refinement procedure
Resolution20.000 - 3.000
R-factor0.27381
Rwork0.271
R-free0.30300

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1pv4
RMSD bond length0.010
RMSD bond angle1.250

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Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0003.120
High resolution limit [Å]3.0003.000
Rmerge0.050

*

0.332

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Number of reflections64912
<I/σ(I)>15.32.5
Completeness [%]96.1

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95
Redundancy2.2

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2.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5

*

4

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0.05 M Cacodylate (pH 6.5), 0.05 M NaCl, 2.5% PEG 8K, 20% glycerol, 0.3 mM n-Nonyl-beta-D-thiomaltoside, 1mM TCEP, VAPOR DIFFUSION, HANGING DROP, temperature 18K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111Cacodylate
1012PEG
1112H2O
211NaCl
311PEG
411glycerol
511n-Nonyl-beta-D-thiomaltoside
611TCEP
711H2O
812Cacodylate
912NaCl
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropTris-HCl10 (mM)pH7.5
21drop50 (mM)
31reservoirsodium cacodylate100 (mM)pH6.5
41reservoir100 (mM)
51reservoirPEG80005 (%)
61reservoirglycerol40 (%)
71reservoirn-Nonyl-beta-D-thiomaltoside0.6 (mM)
81reservoirTCEP2 (mM)

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