5C5A
Crystal Structure of HDM2 in complex with Nutlin-3a
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-06-12 |
Detector | DECTRIS PILATUS 2M-F |
Wavelength(s) | 1.0 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 41.620, 43.630, 52.670 |
Unit cell angles | 90.00, 90.04, 90.00 |
Refinement procedure
Resolution | 41.620 - 1.146 |
R-factor | 0.1537 |
Rwork | 0.153 |
R-free | 0.16830 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4hg7 |
RMSD bond length | 0.014 |
RMSD bond angle | 1.593 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.620 | 1.187 |
High resolution limit [Å] | 1.146 | 1.146 |
Rmerge | 0.068 | |
Number of reflections | 53751 | |
<I/σ(I)> | 12.58 | |
Completeness [%] | 79.1 | 12.95 |
Redundancy | 2.9 | 1.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.2M Potassium iodide, 2.2M Ammonium Sulfate |