6LFC
E. coli Thioesterase I mutant DG
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-07-01 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 73.932, 118.227, 121.286 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 63.000 - 2.700 |
R-factor | 0.228 |
Rwork | 0.227 |
R-free | 0.26100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1u8u |
RMSD bond length | 0.010 |
RMSD bond angle | 1.446 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | MOLREP |
Refinement software | REFMAC (v1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 63.130 | 2.840 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.120 | 1.280 |
Rmeas | 0.128 | 1.379 |
Rpim | 0.050 | 0.512 |
Number of reflections | 30085 | 4352 |
<I/σ(I)> | 14.9 | |
Completeness [%] | 99.9 | |
Redundancy | 12.8 | |
CC(1/2) | 0.999 | 0.836 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | ammonium iodine, peg 3350 |