9HLK
X-ray structure of the adduct formed upon reaction of the diiodido analogue of picoplatin with lysozyme (structure A)
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ELETTRA BEAMLINE 11.2C |
| Synchrotron site | ELETTRA |
| Beamline | 11.2C |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-12-05 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 78.400, 78.400, 36.920 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 55.437 - 1.960 |
| Rwork | 0.206 |
| R-free | 0.26910 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.760 |
| Data reduction software | autoPROC |
| Data scaling software | autoPROC |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 55.440 | 2.000 |
| High resolution limit [Å] | 1.960 | 1.960 |
| Rmerge | 0.067 | 0.966 |
| Rmeas | 0.069 | 0.987 |
| Rpim | 0.015 | 0.204 |
| Number of reflections | 8548 | 381 |
| <I/σ(I)> | 29.9 | 4.1 |
| Completeness [%] | 98.6 | 93.4 |
| Redundancy | 20.9 | 23.3 |
| CC(1/2) | 0.999 | 0.969 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 293 | 1.1 M sodium chloride 0.1 M sodium acetate buffer pH 4.5 |
