8VMG
Crystal structure of GSK-3 26-383 bound to Axin 383-435
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL12-1 |
| Synchrotron site | SSRL |
| Beamline | BL12-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-12-09 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.97946 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 195.585, 195.585, 152.204 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 39.760 - 2.450 |
| R-factor | 0.1953 |
| Rwork | 0.195 |
| R-free | 0.23010 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4nm0 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.841 |
| Data reduction software | XDS |
| Data scaling software | pointless (1.12.2) |
| Phasing software | PHENIX (1.20.1_4487) |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.760 | 2.510 |
| High resolution limit [Å] | 2.450 | 2.450 |
| Rmerge | 0.222 | 8.110 |
| Rmeas | 0.225 | 8.208 |
| Rpim | 0.035 | 1.258 |
| Number of reflections | 63244 | 4331 |
| <I/σ(I)> | 15.9 | 0.7 |
| Completeness [%] | 99.9 | 98.3 |
| Redundancy | 41.1 | 42.2 |
| CC(1/2) | 0.999 | 0.414 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 298 | 100 mM MES, pH 5.5, 1.9 M ammonium sulfate, 200 mM sodium chloride, cryoprotectant: 25% ethylene glycol |






