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3E1J

Crystal structure of E. coli Bacterioferritin (BFR) with an unoccupied ferroxidase centre (APO-BFR).

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID23-1
Synchrotron siteESRF
BeamlineID23-1
Temperature [K]100
Collection date2006-01-01
Spacegroup nameP 42 21 2
Unit cell lengths208.216, 208.216, 142.457
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution35.110 - 2.700
R-factor0.243
Rwork0.242
R-free0.26300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1bcf
RMSD bond length0.017
RMSD bond angle1.817
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.0002.850
High resolution limit [Å]2.7002.700
Number of reflections84897
<I/σ(I)>14.55
Completeness [%]98.893.7
Redundancy6.51.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP52891.8 M AMMONIUM SULFATE, 0.1 M TRI- SODIUM CITRATE PH 5.0. CRYSTALS LATER SOAKED IN CRYOPROTECTANT AT PH 7, VAPOR DIFFUSION, SITTING DROP, TEMPERATURE 289K, pH 5.00

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