5QI8
PanDDA analysis group deposition -- Crystal Structure of human PARP14 Macrodomain 3 in complex with FMOPL000605a
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 | 2017-03-04 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.92819 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 34.552, 41.716, 110.859 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 55.490 - 1.090 |
| R-factor | 0.2026 |
| Rwork | 0.202 |
| R-free | 0.22070 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 4abl |
| RMSD bond length | 0.004 |
| RMSD bond angle | 1.278 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.31) |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 110.860 | 110.860 | 1.150 |
| High resolution limit [Å] | 1.090 | 3.450 | 1.090 |
| Rmerge | 0.034 | 0.030 | 0.176 |
| Rmeas | 0.037 | 0.033 | 0.243 |
| Rpim | 0.015 | 0.014 | 0.167 |
| Total number of observations | 297418 | 13651 | 7347 |
| Number of reflections | 62590 | ||
| <I/σ(I)> | 23.7 | 57.9 | 2.6 |
| Completeness [%] | 92.2 | 98.7 | 57.4 |
| Redundancy | 4.8 | 5.8 | 1.3 |
| CC(1/2) | 0.999 | 0.998 | 0.949 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.4 | 277 | 80 mM KBr, 30 % PEG2kMME |
