6MIQ
Crystal structure of Taf14 YEATS domain in complex with histone H3K9bu
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 4.2.2 |
Synchrotron site | ALS |
Beamline | 4.2.2 |
Temperature [K] | 100 |
Detector technology | CMOS |
Collection date | 2016-06-19 |
Detector | RDI CMOS_8M |
Wavelength(s) | 1.0 |
Spacegroup name | P 65 |
Unit cell lengths | 113.149, 113.149, 26.170 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 56.575 - 1.750 |
R-factor | 0.1745 |
Rwork | 0.172 |
R-free | 0.21780 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5iok |
RMSD bond length | 0.006 |
RMSD bond angle | 0.909 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.11.1_2575)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 98.000 | 1.810 |
High resolution limit [Å] | 1.750 | 1.750 |
Number of reflections | 31249 | |
<I/σ(I)> | 34 | |
Completeness [%] | 99.9 | |
Redundancy | 10.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 44% PEG600 (v/v) and 0.2 M citric acid (pH 6.0) |