7SZ8
Crystal structure of human CELSR1 EC4-7
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-C |
| Synchrotron site | APS |
| Beamline | 24-ID-C |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-03-08 |
| Detector | DECTRIS EIGER2 X 16M |
| Wavelength(s) | 0.97911 |
| Spacegroup name | P 1 |
| Unit cell lengths | 42.384, 76.943, 92.742 |
| Unit cell angles | 89.83, 87.78, 76.23 |
Refinement procedure
| Resolution | 46.378 - 2.337 |
| Rwork | 0.213 |
| R-free | 0.27940 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5t9t 5szn 5v5x 6c13 6e6b 6vg4 |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.752 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.378 | 2.390 |
| High resolution limit [Å] | 2.337 | 2.337 |
| Number of reflections | 47823 | 1953 |
| <I/σ(I)> | 15.375 | 8.824 |
| Completeness [%] | 85.3 | 82.5 |
| Redundancy | 3.3 | 3.2 |
| CC(1/2) | 0.992 | 0.984 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 277 | 0.1 M magnesium chloride, 0.1 M MES pH 7.3, 30% PEG400 |






