5ES3
Co-crystal structure of LDH liganded with oxamate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04-1 |
Synchrotron site | Diamond |
Beamline | I04-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-02-13 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.92 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 84.080, 146.630, 284.900 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 80.642 - 2.290 |
R-factor | 0.1716 |
Rwork | 0.170 |
R-free | 0.20280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4aje |
RMSD bond length | 0.007 |
RMSD bond angle | 0.845 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 80.642 |
High resolution limit [Å] | 2.290 |
Rmerge | 0.127 |
Number of reflections | 158462 |
<I/σ(I)> | 11.9 |
Completeness [%] | 99.7 |
Redundancy | 7.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 291 | 0.1 M Tris/Bicine pH 8.5, 20 % ethylene glycol, 10 % PEG 8000, 0.02 M of each of sodium formate, ammonium acetate, tri-sodium citrate, sodium/potassium tartrate and sodium oxamate |