IMR Press / FBL / Volume 18 / Issue 2 / DOI: 10.2741/4133

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.


Confronting JC virus and Homo sapiens biological signatures

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1 Department of Biochemistry and Molecular Biology, University of Bari, Italy
2 Department of Neurological and Psychiatric Sciences, University of Bari, Italy
Front. Biosci. (Landmark Ed) 2013, 18(2), 716–724;
Published: 1 January 2013

The present report describes the peptide commonality between JC virus (JCV) and the human proteome at the heptamer level. In total, 53 viral heptapeptides occur in functionally important human proteins with potential consequences for host functions and JCV pathogenesis. A paradigmatic example of a crucial peptide match is the SGKTTLA sequence, shared by JCV LT antigen and human nicotinamide/nicotinic acid riboside kinase, an enzyme involved in myelination processes. In general, the JCV- versus-host heptapeptide overlap may result in a competition between viral sequences and identical motifs in host enzymic active sites, adhesive domains, regulatory signaling motifs, etc., thus interfering with essential reactions and posing disadvantages to the cell. Overall, this study provides a starting point for investigating the role of peptide commonality in host- pathogen interactions.

JCV-vrs-human heptapeptide commonality
JCV-associated pathogenesis
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