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1XPR

Structural mechanism of inhibition of the Rho transcription termination factor by the antibiotic 5a-formylbicyclomycin (FB)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 8.3.1
Synchrotron siteALS
Beamline8.3.1
Temperature [K]100
Detector technologyCCD
Wavelength(s)1.100
Spacegroup nameC 1 2 1
Unit cell lengths210.526, 109.679, 160.046
Unit cell angles90.00, 108.16, 90.00
Refinement procedure
Resolution20.000 - 3.150
R-factor0.28389
Rwork0.274
R-free0.29582
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.006
RMSD bond angle1.081
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0003.230
High resolution limit [Å]3.1503.150
Number of reflections49136
Completeness [%]86.576.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION6.5293PEG 3350, Na Cacodylate, NaCl, glycerol, Na DihydrogenPhosphate, pH 6.5, VAPOR DIFFUSION, temperature 293K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111PEG 3350
211NaCl
311glycerol
411NaH2PO4
511sodium Cacodylate
612PEG 3350
712NaCl
812glycerol
912NaH2PO4

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PDB entries from 2024-07-24

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