3EEX
The crystal structure of OspA mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-03-13 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.9793 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 36.502, 82.401, 109.428 |
Unit cell angles | 90.00, 91.62, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.490 |
R-factor | 0.26578 |
Rwork | 0.262 |
R-free | 0.29875 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3cka |
RMSD bond length | 0.013 |
RMSD bond angle | 1.559 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.590 |
High resolution limit [Å] | 2.490 | 2.490 |
Rmerge | 0.094 | 0.616 |
Number of reflections | 22424 | |
<I/σ(I)> | 2.33 | |
Completeness [%] | 99.0 | 100 |
Redundancy | 3.1 | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 9 | 293 | 34% PEG400, 0.1M Tris-HCl pH 9, protein 20.2 mg/ml, VAPOR DIFFUSION, HANGING DROP, temperature 293K |