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This mini-review describes the structural and functional aspects of the cardiac channel protein Nav1.5, its post-translational modifications, and its role in human channelopathies.
This review summarizes the structural and functional aspects of the cardiac Nav1.5 protein and its role in human channelopathies.
The aim of this mini-review is to draw together the main concepts and findings that have emerged from recent studies of the cardiac channel protein Nav1.5. This complex protein is encoded by the SCN5A gene that, in its mutated form, is implicated in various diseases, particularly channelopathies, specifically at cardiac tissue level. Here we describe the structural, and functional aspects of Nav1.5 including post-translational modifications in normal conditions, and the main human channelopathies in which this protein may be the cause or trigger. Lastly, we also briefly discuss interacting proteins that are relevant for these channel functions in normal and disease conditions.
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Detta et al. (2015) conducted a review in Cardiac channelopathies. Nav1.5 protein was evaluated. This mini-review describes the structural and functional aspects of the cardiac channel protein Nav1.5, its post-translational modifications, and its role in human channelopathies.
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