8AIK
Crystal structure of DltE from L. plantarum, tartare bound form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID30B |
Synchrotron site | ESRF |
Beamline | ID30B |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-05-15 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9677 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.690, 103.730, 152.529 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.384 - 1.950 |
Rwork | 0.182 |
R-free | 0.22110 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 8agr |
RMSD bond length | 0.007 |
RMSD bond angle | 1.433 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0352) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.384 | 2.000 |
High resolution limit [Å] | 1.950 | 1.950 |
Rmerge | 0.050 | 0.564 |
Number of reflections | 56946 | 3918 |
<I/σ(I)> | 14.5 | 2.4 |
Completeness [%] | 99.5 | |
Redundancy | 4.5 | |
CC(1/2) | 0.999 | 0.787 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | PEG 3350, ammonium tartrate |