6L1F
Crystal structure of PHF20L1 Tudor1 in complex with K142me1 DNMT1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-04-14 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 42.702, 52.932, 31.394 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.235 - 1.900 |
R-factor | 0.196 |
Rwork | 0.192 |
R-free | 0.22970 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3sd4 |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.240 | 1.930 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.119 | 0.541 |
Number of reflections | 5921 | 553 |
<I/σ(I)> | 16.9 | 2.1 |
Completeness [%] | 99.0 | |
Redundancy | 6.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 30% PEG MME 2000, 0.1M sodium cacodylate, pH 6.0 |