8HKO
Mutated human ADP-ribosyltransferase 2 (PARP2) catalytic domain bound to Rucaparib
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL02U1 |
| Synchrotron site | SSRF |
| Beamline | BL02U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-12-14 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.97918 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 39.761, 86.286, 96.047 |
| Unit cell angles | 90.00, 90.39, 90.00 |
Refinement procedure
| Resolution | 36.650 - 2.100 |
| R-factor | 0.1659 |
| Rwork | 0.164 |
| R-free | 0.21080 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | Alphafold model |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.417 |
| Data scaling software | Aimless |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.650 | 2.175 |
| High resolution limit [Å] | 2.100 | 2.100 |
| Number of reflections | 37874 | 3743 |
| <I/σ(I)> | 17.08 | 5.5 |
| Completeness [%] | 99.8 | 99.97 |
| Redundancy | 5.9 | |
| CC(1/2) | 0.997 | 0.942 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 291 | 25% PEG-3350, 0.1 M Tris-HCl pH 8.5 |






