IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v457y2009i7228d10.1038_nature07529.html
   My bibliography  Save this article

Protein kinase R reveals an evolutionary model for defeating viral mimicry

Author

Listed:
  • Nels C. Elde

    (Division of Basic Sciences,)

  • Stephanie J. Child

    (and)

  • Adam P. Geballe

    (and
    Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA
    University of Washington, Seattle, Washington 98115, USA)

  • Harmit S. Malik

    (Division of Basic Sciences,)

Abstract

Virus versus innate immunity Poxviruses, such as small pox, undermine host defences by producing a protein called K3L, which closely mimics the substrate of protein kinase R (PKR), an important component of the vertebrate innate immunity system. Elde et al. show that PKR evolved under dramatic episodes of positive selection in primates, substituting amino acids at sites where K3L and PKR meet. The evolutionary changes increase the chances of the host defeating the mimic and see the two protagonists locked in a molecular 'arms race' trying to out-smart and out-evolve each other.

Suggested Citation

  • Nels C. Elde & Stephanie J. Child & Adam P. Geballe & Harmit S. Malik, 2009. "Protein kinase R reveals an evolutionary model for defeating viral mimicry," Nature, Nature, vol. 457(7228), pages 485-489, January.
  • Handle: RePEc:nat:nature:v:457:y:2009:i:7228:d:10.1038_nature07529
    DOI: 10.1038/nature07529
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature07529
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature07529?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Joseph Hiatt & Judd F. Hultquist & Michael J. McGregor & Mehdi Bouhaddou & Ryan T. Leenay & Lacy M. Simons & Janet M. Young & Paige Haas & Theodore L. Roth & Victoria Tobin & Jason A. Wojcechowskyj & , 2022. "A functional map of HIV-host interactions in primary human T cells," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:457:y:2009:i:7228:d:10.1038_nature07529. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.