13QJ
PanDDA analysis group deposition -- Crystal structure of PLpro-C111S in complex with 7T-0223
This is a non-PDB format compatible entry.
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 | 2024-05-09 |
| Detector | DECTRIS EIGER2 S 9M |
| Wavelength(s) | 0.97918 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 83.000, 83.000, 133.860 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 37.910 - 2.580 |
| R-factor | 0.1969 |
| Rwork | 0.196 |
| R-free | 0.22520 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 7cjm |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.445 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.7.7) |
| Phasing software | DIMPLE |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 37.910 | 37.910 | 2.650 |
| High resolution limit [Å] | 2.580 | 11.540 | 2.580 |
| Rmerge | 0.103 | 0.028 | 1.715 |
| Rmeas | 0.106 | 0.030 | 1.757 |
| Rpim | 0.024 | 0.008 | 0.381 |
| Total number of observations | 342645 | 2815 | 26008 |
| Number of reflections | 17355 | 229 | 1237 |
| <I/σ(I)> | 24.1 | 59 | 2.4 |
| Completeness [%] | 99.9 | 97.2 | 99.9 |
| Redundancy | 19.7 | 12.3 | 21 |
| CC(1/2) | 1.000 | 1.000 | 0.867 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6 | 291 | 1.4 M Sodium Maleate pH 6.0 |
