6MBA
Crystal Structure of Human Nav1.4 CTerminal Domain in Complex with apo Calmodulin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 17-ID-1 |
| Synchrotron site | NSLS-II |
| Beamline | 17-ID-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-10-02 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 0.918 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 112.720, 29.041, 94.991 |
| Unit cell angles | 90.00, 123.65, 90.00 |
Refinement procedure
| Resolution | 44.875 - 1.799 |
| R-factor | 0.2043 |
| Rwork | 0.203 |
| R-free | 0.23350 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4ovn |
| RMSD bond length | 0.016 |
| RMSD bond angle | 1.384 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 44.875 | 44.500 | 1.850 |
| High resolution limit [Å] | 1.799 | 8.050 | 1.800 |
| Rmerge | 0.060 | 0.046 | 0.429 |
| Rmeas | 0.084 | 0.065 | 0.591 |
| Number of reflections | 42682 | 452 | 3101 |
| <I/σ(I)> | 6.57 | 13.37 | 1.53 |
| Completeness [%] | 91.4 | 85.8 | 90.6 |
| Redundancy | 1.605 | 1.712 | 1.581 |
| CC(1/2) | 0.991 | 0.987 | 0.825 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 6 | 293 | 0.1M MES pH 6.0, 20% PEG 6000, 1.0M LiCl |






