8R0Z
14-3-3 sigma in complex with TAZ peptide and stabilizing fragment TCF199
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID23-1 |
| Synchrotron site | ESRF |
| Beamline | ID23-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-10-13 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.97626 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 81.474, 111.984, 62.754 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 65.880 - 1.200 |
| R-factor | 0.169 |
| Rwork | 0.169 |
| R-free | 0.17560 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.911 |
| Data reduction software | DIALS |
| Data scaling software | Aimless |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 65.880 | 1.220 |
| High resolution limit [Å] | 1.200 | 1.200 |
| Rmerge | 0.075 | 0.529 |
| Rmeas | 0.081 | 0.575 |
| Number of reflections | 89634 | 8853 |
| <I/σ(I)> | 17.4 | |
| Completeness [%] | 100.0 | |
| Redundancy | 12.8 | |
| CC(1/2) | 0.997 | 0.940 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 277.15 | 0.095M HEPES pH 7.5, 26%PEG 400, 0.19M CaCL, 5%Glycerol |






