8A0U
Crystal structure of TEAD3 in complex with CPD4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-12-12 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.0000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 65.265, 128.607, 156.107 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.640 - 2.895 |
R-factor | 0.2144 |
Rwork | 0.212 |
R-free | 0.26800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Previous in-house structure |
RMSD bond length | 0.008 |
RMSD bond angle | 1.000 |
Data reduction software | autoPROC |
Data scaling software | STARANISO |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.8 (3-FEB-2022)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 24.638 | 2.980 |
High resolution limit [Å] | 2.895 | 2.895 |
Rmerge | 0.158 | 0.741 |
Number of reflections | 27738 | 1388 |
<I/σ(I)> | 10.5 | 2.4 |
Completeness [%] | 92.2 | |
Redundancy | 6.5 | |
CC(1/2) | 0.997 | 0.823 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 1.1 - 1.4 M sodium/potassium phosphate pH 5.6 |