8AEU
Structure of hMDM2 in complex with Nutlin-3a-aa
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-07-11 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9184 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 56.233, 56.233, 75.376 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.070 - 2.000 |
R-factor | 0.2012 |
Rwork | 0.197 |
R-free | 0.24040 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4zfi |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.15.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.070 | 2.050 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.048 | |
Number of reflections | 8645 | 6799 |
<I/σ(I)> | 33.6 | |
Completeness [%] | 100.0 | |
Redundancy | 24.7 | |
CC(1/2) | 1.000 | 0.805 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.01 M magnesium chloride hexahydrate, 0.05 M Tris hydrochloride pH 7.6, 1.6 M ammonium sulfate |