6HK9
Crystal structure of TEX12 F102A F109E V116A
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I24 |
Synchrotron site | Diamond |
Beamline | I24 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-07-08 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9790 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 43.233, 219.712, 37.501 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.971 - 1.454 |
R-factor | 0.1808 |
Rwork | 0.179 |
R-free | 0.20470 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Quark decoys |
RMSD bond length | 0.008 |
RMSD bond angle | 0.856 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | AMPLE |
Refinement software | PHENIX ((dev_3126: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 54.930 | 1.480 |
High resolution limit [Å] | 1.450 | 1.450 |
Rmeas | 0.044 | 0.472 |
Rpim | 0.017 | 0.170 |
Number of reflections | 59176 | |
<I/σ(I)> | 20.3 | 2.6 |
Completeness [%] | 98.1 | 96.6 |
Redundancy | 7.1 | |
CC(1/2) | 0.999 | 0.993 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 200 mM Calcium acetate, 40% MPD |