8RRM
tripartite complex between 14-3-3 sigma, Fusicoccin-A, and a phosphopeptide optimized for a Fusicoccin-mediated stabilization of the complex
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 | 2023-02-16 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.8856 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 138.330, 55.910, 82.750 |
Unit cell angles | 90.00, 101.71, 90.00 |
Refinement procedure
Resolution | 47.440 - 2.000 |
R-factor | 0.185 |
Rwork | 0.183 |
R-free | 0.21860 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.011 |
RMSD bond angle | 0.878 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((1.21rc1_5015: ???)) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 47.440 | 47.440 | 1.910 |
High resolution limit [Å] | 1.800 | 5.370 | 1.800 |
Rmerge | 0.072 | 0.030 | 3.282 |
Rmeas | 0.085 | 0.036 | 3.846 |
Number of reflections | 111525 | 4191 | 17959 |
<I/σ(I)> | 7.81 | ||
Completeness [%] | 99.1 | ||
Redundancy | 3.56 | ||
CC(1/2) | 0.999 | 0.999 | 0.216 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 277 | 20% PEG 6000, 100mM Tris pH 8.5 |