9I6T
14-3-3sigma binding to the ERa peptide and compound 32
This is a non-PDB format compatible entry.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-2 |
Synchrotron site | ESRF |
Beamline | ID23-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2024-06-14 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.873128 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 82.191, 113.033, 62.894 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 56.580 - 1.300 |
R-factor | 0.1296 |
Rwork | 0.128 |
R-free | 0.15383 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.009 |
RMSD bond angle | 1.179 |
Data reduction software | autoPROC |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | PDB-REDO |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 62.890 | 1.320 |
High resolution limit [Å] | 1.300 | 1.300 |
Number of reflections | 72119 | 3565 |
<I/σ(I)> | 21.7 | 3.7 |
Completeness [%] | 99.9 | |
Redundancy | 11.8 | |
CC(1/2) | 1.000 | 0.881 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.095 M HEPES pH=7.1-7.7 0.19 M CaCl2 5% glycerol 24-29% PEG400 |