7ONT
PARP1 catalytic domain in complex with a selective pyridine carboxamide-based inhibitor (compound 22)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-10-05 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.97625 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.573, 92.621, 164.312 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 82.160 - 1.853 |
R-factor | 0.2146 |
Rwork | 0.213 |
R-free | 0.24380 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | internal model |
RMSD bond length | 0.008 |
RMSD bond angle | 0.970 |
Data reduction software | XDS |
Data scaling software | STARANISO |
Phasing software | AMoRE |
Refinement software | BUSTER (2.11.8 (24-FEB-2021)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 82.160 | 1.989 |
High resolution limit [Å] | 1.850 | 1.850 |
Rmerge | 0.143 | 1.354 |
Number of reflections | 50296 | 2516 |
<I/σ(I)> | 9.2 | 1.5 |
Completeness [%] | 93.3 | |
Redundancy | 6.5 | |
CC(1/2) | 0.997 | 0.482 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 9.5 | 293 | 2.5 M ammonium sulfate, 0.1 M Tris pH 8.5 |