5QHT
PanDDA analysis group deposition -- Crystal Structure of human PARP14 Macrodomain 3 in complex with FMOPL000065a
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04-1 |
| Synchrotron site | Diamond |
| Beamline | I04-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-02-09 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.92819 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 34.200, 41.390, 111.370 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 55.750 - 1.050 |
| R-factor | 0.1875 |
| Rwork | 0.186 |
| R-free | 0.21330 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 4abl |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.172 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.31) |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 55.690 | 55.690 | 1.080 |
| High resolution limit [Å] | 1.050 | 4.580 | 1.050 |
| Rmerge | 0.044 | 0.040 | 0.254 |
| Rmeas | 0.048 | 0.044 | 0.328 |
| Rpim | 0.019 | 0.018 | 0.204 |
| Total number of observations | 295735 | 5919 | 938 |
| Number of reflections | 53278 | ||
| <I/σ(I)> | 20.9 | 43.1 | 2.4 |
| Completeness [%] | 71.5 | 98.6 | 9.3 |
| Redundancy | 5.6 | 5.8 | 1.8 |
| CC(1/2) | 0.998 | 0.997 | 0.931 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.4 | 277 | 80 mM KBr, 30 % PEG2kMME |
