6E1F
Crystal structure of the SWIRM domain of human histone lysine-specific demethylase LSD1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-03-01 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.97857 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 49.957, 57.514, 97.019 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.180 - 1.160 |
R-factor | 0.133 |
Rwork | 0.133 |
R-free | 0.16900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5it3 |
RMSD bond length | 0.015 |
RMSD bond angle | 1.907 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0230) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.180 | 1.190 |
High resolution limit [Å] | 1.160 | 1.160 |
Number of reflections | 94426 | |
<I/σ(I)> | 50.7 | 3.5 |
Completeness [%] | 96.8 | 86.4 |
Redundancy | 11.4 | 8.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 293 | 0.1 M Bis-Tris, pH 6.5, 0.1 M potassium chloride, 1.5 M ammonium sulfate |