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3E1O

Crystal structure of E. coli Bacterioferritin (BFR) with two ZN(II) ION sites at the Ferroxidase centre (ZN-BFR).

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX10.1
Synchrotron siteSRS
BeamlinePX10.1
Temperature [K]100
Detector technologyCCD
Collection date2006-01-01
Spacegroup nameP 42 21 2
Unit cell lengths207.867, 207.867, 142.432
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.810 - 2.950
R-factor0.23
Rwork0.229
R-free0.25200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2QP7
RMSD bond length0.022
RMSD bond angle1.941
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.0003.110
High resolution limit [Å]2.9502.950
Number of reflections58778
<I/σ(I)>20.97.9
Completeness [%]89.289.2
Redundancy9.16.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5298APO-BFR CRYSTALIZED IN 1.8 M AMMONIUM SULFATE, 0.1 M TRI-SODIUM CITRATE PH 5.0. CRYSTAL WAS THEN SOAKED IN A CRYOPROTECTANT CONTAINING ZN2+ IONS AND BUFFERED WITH MOPS PH 7 INSTEAD OF CITRATE. PLEASE SEE PAPER FO FULL DETAILS., VAPOR DIFFUSION, SITTING DROP, TEMPERATURE 298K, pH 5.00

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