6UYB
Crystal structure of TEAD2 bound to Compound 1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.2 |
Synchrotron site | ALS |
Beamline | 5.0.2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-08-28 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.999 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 124.418, 62.090, 79.620 |
Unit cell angles | 90.00, 117.82, 90.00 |
Refinement procedure
Resolution | 70.417 - 1.543 |
R-factor | 0.1976 |
Rwork | 0.196 |
R-free | 0.23190 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5emv |
Data reduction software | ADDREF |
Data scaling software | autoPROC |
Phasing software | PHENIX |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 70.417 | 1.710 |
High resolution limit [Å] | 1.543 | 1.543 |
Number of reflections | 39934 | 1997 |
<I/σ(I)> | 13 | |
Completeness [%] | 86.0 | |
Redundancy | 3.3 | |
CC(1/2) | 0.999 | 0.609 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 292 | 200 mM potassium/sodium tartrate pH 6.5 20% PEG 3350 |