4Y17
SdiA in complex with 3-oxo-C8-homoserine lactone
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 | 2011-12-02 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.987 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 88.486, 92.430, 118.995 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.469 - 2.840 |
R-factor | 0.2363 |
Rwork | 0.234 |
R-free | 0.27120 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4y13 |
RMSD bond length | 0.004 |
RMSD bond angle | 0.902 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX ((phenix.refine: 1.8.4_1496)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.469 | |
High resolution limit [Å] | 2.840 | 2.840 |
Number of reflections | 23551 | |
<I/σ(I)> | 22.4 | 2.1 |
Completeness [%] | 99.5 | 99.7 |
Redundancy | 5 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 18% (w/v) PEG 3350, 0.1M sodium acetate pH5.4, 0.3M ammonium sulfate |