5ONN
Crystal Structure of Ectoine Synthase from P. lautus
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-10-21 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.988 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 70.910, 70.910, 68.540 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 45.737 - 1.400 |
R-factor | 0.1828 |
Rwork | 0.182 |
R-free | 0.19920 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5bxx |
RMSD bond length | 0.010 |
RMSD bond angle | 1.651 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 45.737 |
High resolution limit [Å] | 1.200 |
Rmerge | 0.060 |
Number of reflections | 53471 |
<I/σ(I)> | 24.6 |
Completeness [%] | 91.9 |
Redundancy | 20 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | BATCH MODE | 4.2 | 298 | 0.2 M ammonium sulfate, 0.1 M phosphate citrate pH 4.2, 20% (v/v) PEG 300, 10% (v/v) glycerol. |