6OAK
Structure of human PARG complexed with JA2131
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL9-2 |
| Synchrotron site | SSRL |
| Beamline | BL9-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-12-14 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.979 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 66.497, 89.333, 94.161 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 37.078 - 1.700 |
| R-factor | 0.1835 |
| Rwork | 0.182 |
| R-free | 0.20880 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4b1g |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.799 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.10_2155: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 37.078 | 1.761 |
| High resolution limit [Å] | 1.700 | 1.700 |
| Rmerge | 0.139 | 2.688 |
| Number of reflections | 62296 | 6098 |
| <I/σ(I)> | 17.71 | |
| Completeness [%] | 100.0 | 99 |
| Redundancy | 19.1 | 13.1 |
| CC(1/2) | 0.999 | 0.431 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 295 | 0.1 M PCTP, pH 7.5, 0.2 M (NH3)2SO4, 17% PEG3350 |






