7EID
Crystal structure of AF9 YEATS domain in complex with H4K8acK12ac peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL26B2 |
Synchrotron site | SPring-8 |
Beamline | BL26B2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-10-02 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 1.000 |
Spacegroup name | P 1 |
Unit cell lengths | 42.963, 44.913, 58.797 |
Unit cell angles | 84.86, 86.09, 66.33 |
Refinement procedure
Resolution | 39.360 - 2.000 |
R-factor | 0.20381 |
Rwork | 0.202 |
R-free | 0.22881 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4tmp |
RMSD bond length | 0.002 |
RMSD bond angle | 0.790 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.030 |
High resolution limit [Å] | 1.996 | 2.000 |
Number of reflections | 26432 | 1339 |
<I/σ(I)> | 13.9 | |
Completeness [%] | 97.3 | |
Redundancy | 2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 200 mM ammonium citrate tribasic buffer (pH 7.0) containing 19% PEG3350 |