9SPR
p53 cancer mutant R282W in complex with DARPin C10
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SLS BEAMLINE X06SA |
| Synchrotron site | SLS |
| Beamline | X06SA |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2023-02-05 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 37.587, 93.837, 53.263 |
| Unit cell angles | 90.00, 109.94, 90.00 |
Refinement procedure
| Resolution | 46.900 - 1.660 |
| R-factor | 0.153198508844 |
| Rwork | 0.151 |
| R-free | 0.20069 |
| Structure solution method | FOURIER SYNTHESIS |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.751 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.900 | 1.690 |
| High resolution limit [Å] | 1.660 | 1.660 |
| Rmerge | 0.069 | 0.628 |
| Number of reflections | 40703 | 2011 |
| <I/σ(I)> | 11.1 | 2 |
| Completeness [%] | 99.4 | 98.7 |
| Redundancy | 5 | 5.3 |
| CC(1/2) | 0.998 | 0.858 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | Protein concentration: 1.8 mg/ml in 25 mM HEPES pH 7.5, 150 mM NaCl, 0.5 mM TCEP. Reservoir buffer: 25% PEG3350, 0.1M HEPES pH 7.5, 0.2M lithium sulfate. Drop volume ratio 1:1. |






