6SYG
Crystal structure of the Cyclic Nucleotide-Binding Homology Domain of the human KCNH2 channel
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-04-12 |
Detector | DECTRIS PILATUS 6M-F |
Wavelength(s) | 0.972 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 57.493, 90.649, 61.111 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.550 - 1.500 |
R-factor | 0.1706 |
Rwork | 0.170 |
R-free | 0.18400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4llo |
RMSD bond length | 0.008 |
RMSD bond angle | 1.058 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.580 | 1.590 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmeas | 0.114 | 0.811 |
Number of reflections | 25875 | 4087 |
<I/σ(I)> | 13.91 | |
Completeness [%] | 99.7 | |
Redundancy | 11.5 | |
CC(1/2) | 0.999 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 292 | 20% w/v PEG 3350, 2% v/v Tacsimate, 0.1M Bis-Tris, pH 6.8 |