6V3Y
Crystal structure of EED in complex with PALI1-K1219me3 peptide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-07-24 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.95372 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 57.775, 85.296, 91.106 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 48.790 - 1.630 |
| R-factor | 0.1665 |
| Rwork | 0.165 |
| R-free | 0.19250 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3jzn |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.890 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.5) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.790 | 1.710 |
| High resolution limit [Å] | 1.630 | 1.630 |
| Rmerge | 0.074 | 0.643 |
| Number of reflections | 57098 | 8025 |
| <I/σ(I)> | 16.2 | |
| Completeness [%] | 99.7 | 97.9 |
| Redundancy | 8.1 | 8.1 |
| CC(1/2) | 0.866 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | 3.6 M sodium formate, 10 mM TCEP, 5% glycerol |






