3H94
Crystal structure of the membrane fusion protein CusB from Escherichia coli
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-03-29 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.3779,0.9792,0.9793,0.9949 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 85.005, 114.418, 259.080 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.200 - 3.840 |
R-factor | 0.28 |
Rwork | 0.280 |
R-free | 0.30000 |
Structure solution method | MAD |
RMSD bond length | 0.010 |
RMSD bond angle | 1.900 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SHARP |
Refinement software | PHENIX |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 3.980 |
High resolution limit [Å] | 3.840 | 3.840 |
Rmerge | 0.072 | 0.412 |
Number of reflections | 363533 | |
<I/σ(I)> | 24 | 7.5 |
Completeness [%] | 99.4 | 95.2 |
Redundancy | 3.8 | 3.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 5.6 | 298 | 15%PEG1000, 360mM Lithium Citrate, 5% Glycerol, 5% Isopropanol, pH 5.6, VAPOR DIFFUSION, temperature 298K |