3OON
The structure of an outer membrance protein from Borrelia burgdorferi B31
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-06-09 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9793 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 52.089, 74.784, 66.760 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.740 - 1.790 |
R-factor | 0.2136 |
Rwork | 0.212 |
R-free | 0.23614 |
Structure solution method | SAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.147 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | SHELXD |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.830 |
High resolution limit [Å] | 1.790 | 1.800 |
Rmerge | 0.069 | 0.210 |
Number of reflections | 12430 | |
<I/σ(I)> | 50.6 | 7.35 |
Completeness [%] | 98.4 | 100 |
Redundancy | 5.3 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 277 | 0.20M ammonium sulfate, 0.1M bis-tris, 25%w/v PEG3350, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 277K |