5C9B
Crystal structure of a retropepsin-like aspartic protease from Rickettsia conorii
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-10-20 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.9825 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 101.985, 101.985, 127.063 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.370 - 2.400 |
R-factor | 0.20206 |
Rwork | 0.199 |
R-free | 0.26222 |
RMSD bond length | 0.016 |
RMSD bond angle | 1.819 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | SOLVE |
Refinement software | REFMAC (5.7.0032) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.440 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.054 | 0.419 |
Number of reflections | 28761 | |
<I/σ(I)> | 31.27 | 2.67 |
Completeness [%] | 87.6 | 33.6 |
Redundancy | 5.6 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.8 | 293 | 24% PEG4000, 0.2 M lithium sulfate, pH 5.8 |