9DFR
PARP4 BRCT domain F39A mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08B1-1 |
Synchrotron site | CLSI |
Beamline | 08B1-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2024-04-02 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.2 |
Spacegroup name | F 2 3 |
Unit cell lengths | 115.411, 115.411, 115.411 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.520 - 1.900 |
R-factor | 0.18342 |
Rwork | 0.182 |
R-free | 0.21838 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.004 |
RMSD bond angle | 1.257 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0430) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.950 |
High resolution limit [Å] | 1.900 | 1.900 |
Number of reflections | 10148 | 687 |
<I/σ(I)> | 22.3 | |
Completeness [%] | 99.9 | 100 |
Redundancy | 8.6 | 8.4 |
CC(1/2) | 0.999 | 0.607 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 27% PEG3350, 0.2M ammonium sulfate and 0.1M sodium acetate pH 4.6 |