5RKR
PanDDA analysis group deposition -- Crystal Structure of PHIP in complex with Z1432018343
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 | 2019-07-28 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.97622 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 81.270, 27.080, 55.980 |
| Unit cell angles | 90.00, 100.33, 90.00 |
Refinement procedure
| Resolution | 39.980 - 1.370 |
| R-factor | 0.1879 |
| Rwork | 0.186 |
| R-free | 0.22000 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 3mb3 |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.860 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.7.4) |
| Phasing software | REFMAC |
| Refinement software | BUSTER (2.10.3 (29-NOV-2019)) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 39.980 | 39.980 | 1.410 |
| High resolution limit [Å] | 1.370 | 6.130 | 1.370 |
| Rmerge | 0.050 | 0.022 | 0.812 |
| Rmeas | 0.061 | 0.027 | 1.037 |
| Rpim | 0.033 | 0.015 | 0.638 |
| Total number of observations | 74498 | 910 | 3795 |
| Number of reflections | 25299 | ||
| <I/σ(I)> | 11.6 | 38.9 | 1 |
| Completeness [%] | 98.8 | 95.8 | 97 |
| Redundancy | 2.9 | 2.9 | 2.1 |
| CC(1/2) | 0.999 | 0.999 | 0.560 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.6 | 277 | 20% PEG 8000, 0.04M potassium phosphate |
