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    Repetitive sequences in malaria parasite proteins

    Davies, H. and Nofal, S. and Mclaughlin, E. and Osborne, Andrew (2017) Repetitive sequences in malaria parasite proteins. FEMS Microbiology Reviews 41 (6), pp. 923-940. ISSN 1574-6976.

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    Abstract

    Five species of parasite cause malaria in humans with the most severe disease caused by Plasmodium falciparum. Many of the proteins encoded in the P. falciparum genome are unusually enriched in repetitive low complexity sequences containing a limited repertoire of amino acids. These repetitive sequences expand and contract dynamically and are among the most rapidly changing sequences in the genome. The simplest repetitive sequences consist of single amino acid repeats such as poly-asparagine tracts which are found in approximately 25% of P. falciparum proteins. More complex repeats of two or more amino acids are also common in diverse parasite protein families. There is no universal explanation for the occurrence of repetitive sequences and it is possible that many confer no function to the encoded protein and no selective advantage or disadvantage to the parasite. However, there are increasing numbers of examples where repetitive sequences are important for parasite protein function. We discuss the diverse roles of low complexity repetitive sequences throughout the parasite life cycle, from mediating protein-protein interactions to enabling the parasite to evade the host immune system.

    Metadata

    Item Type: Article
    Additional Information: This is a pre-copyedited, author-produced PDF of an article accepted for publication following peer review. The version of record is available online at the link above.
    Keyword(s) / Subject(s): malaria, Plasmodium falciparum, protein repeats, low complexity, host-pathogen interaction, protein evolution
    School: Birkbeck Faculties and Schools > Faculty of Science > School of Natural Sciences
    Depositing User: Andrew Osborne
    Date Deposited: 07 Dec 2017 06:54
    Last Modified: 02 Aug 2023 17:37
    URI: https://eprints.bbk.ac.uk/id/eprint/20547

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