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. 2021 Jan 13;11:944. doi: 10.1038/s41598-020-79580-9

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Schematic model of the multiple PBM-mediated interactions of HBc with PTPN3 and other PDZ-containing proteins. The model illustrates the competition of HBc with PTPN3 cellular ligands (CNP, PTB). The subsequent complex formed between the two proteins could allow the dephosphorylation of HBc by PTPN3, potentially affecting capsid stability. HBc could also target and alter functions of other cellular PDZ-containing proteins (proteins X, Y, Z).