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. 2018 Sep 29;12(1):326–334. doi: 10.1080/19336950.2018.1516984

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© 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 1. — Location of predicted phosphorylation sites within human Ca_v2.3d. (a). Cartoon of the deduced transmembrane organization of the human Ca_v2.3d subunit. (b). Predicted phosphorylation sites within the amino terminus, the I-II loop and the II-III loop. (c). and (d). Predicted phosphorylation sites within the carboxy terminus including a cluster of putative phosphorylation sites for PKC, PKA and tyrosine kinase downstream of important functional domains (EF-like and IQ site as well as the inserted exon 45 of the splice variant d of Ca_v2.3). (E). A detailed view of the alternate exons 19 and 45, which are identified in different Ca_v2.3 splice variants (for details see 53) is shown. Note within exon 45 one additional PKC site, which was predicted.