6DUW
Crystal structure of the alpha-N-catenin actin-binding domain H1 mutant
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | CLSI BEAMLINE 08ID-1 |
| Synchrotron site | CLSI |
| Beamline | 08ID-1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-04-15 |
| Detector | RAYONIX MX-300 |
| Wavelength(s) | 1 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 108.652, 108.652, 133.078 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 42.080 - 2.200 |
| R-factor | 0.204 |
| Rwork | 0.202 |
| R-free | 0.22630 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4k1o |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.789 |
| Data reduction software | HKL-2000 |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 42.080 | 2.280 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.076 | 0.680 |
| Number of reflections | 24191 | |
| <I/σ(I)> | 31.7 | 3.6 |
| Completeness [%] | 99.8 | 100 |
| Redundancy | 13.1 | 13.3 |
| CC(1/2) | 0.980 | 0.890 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 277 | 2.0 M ammonium sulfate, 10 mM cobalt chloride |






