8WMO
Crystal structure analysis of tubulin and heterocyclic podophyllotoxins complex for anticancer agents
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 | 2022-01-03 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.987 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 103.820, 156.446, 179.393 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.860 - 2.890 |
R-factor | 0.2259 |
Rwork | 0.224 |
R-free | 0.26620 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.011 |
RMSD bond angle | 1.276 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.996 |
High resolution limit [Å] | 2.890 | 2.893 |
Number of reflections | 65706 | 6356 |
<I/σ(I)> | 71.89 | |
Completeness [%] | 99.6 | |
Redundancy | 6.7 | |
CC(1/2) | 0.850 | 0.750 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 277 | 6% glycerol, 6% PEG4000, 30 mM MgCl2, 30 mM CaCl2, 100 mM MES-Na |