5ONM
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 | 71.130, 71.130, 68.660 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 35.565 - 1.520 |
R-factor | 0.1776 |
Rwork | 0.176 |
R-free | 0.20280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5bxx |
RMSD bond length | 0.011 |
RMSD bond angle | 1.405 |
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] | 35.565 |
High resolution limit [Å] | 1.520 |
Number of reflections | 31125 |
<I/σ(I)> | 19.2 |
Completeness [%] | 99.3 |
Redundancy | 18.8 |
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. |