3E1J
Crystal structure of E. coli Bacterioferritin (BFR) with an unoccupied ferroxidase centre (APO-BFR).
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Collection date | 2006-01-01 |
Spacegroup name | P 42 21 2 |
Unit cell lengths | 208.216, 208.216, 142.457 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.110 - 2.700 |
R-factor | 0.243 |
Rwork | 0.242 |
R-free | 0.26300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1bcf |
RMSD bond length | 0.017 |
RMSD bond angle | 1.817 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.000 | 2.850 |
High resolution limit [Å] | 2.700 | 2.700 |
Number of reflections | 84897 | |
<I/σ(I)> | 14.5 | 5 |
Completeness [%] | 98.8 | 93.7 |
Redundancy | 6.5 | 1.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5 | 289 | 1.8 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 |