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 |