5N7I
Crystal structure of the coiled-coil domain of human tricellulin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-05-13 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.918409 |
Spacegroup name | P 42 |
Unit cell lengths | 95.711, 95.711, 34.615 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.860 - 2.880 |
R-factor | 0.212 |
Rwork | 0.210 |
R-free | 0.23800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5n7h |
RMSD bond length | 0.010 |
RMSD bond angle | 0.980 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | BUSTER (2.10.3) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.860 | 3.220 |
High resolution limit [Å] | 2.879 | 2.880 |
Rmerge | 0.079 | 1.332 |
Number of reflections | 7271 | 711 |
<I/σ(I)> | 14.62 | 1.33 |
Completeness [%] | 98.4 | 98.78 |
Redundancy | 5.4 | 5.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 8.5% (w/v) PEG4000, 20% 2-propanol, 0.1 M HEPES-NaOH pH 7.0 |