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  • Pex13p Is an SH3 Protein of the Peroxisome Membrane and a Docking Factor for the Predominantly Cytoplasmic PTS1 Receptor

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    Author(s)
    Gould, SJ
    Kalish, JE
    Morrell, JC
    Bjorkman, J
    Urquhart, AJ
    Crane, DI
    Griffith University Author(s)
    Crane, Denis I.
    Year published
    1996
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    Abstract
    Import of newly synthesized PTS1 proteins into the peroxisome requires the PTS1 receptor (Pex5p), a predominantly cytoplasmic protein that cycles between the cytoplasm and peroxisome. We have identified Pex13p, a novel integral peroxisomal membrane from both yeast and humans that binds the PTS1 receptor via a cytoplasmically oriented SH3 domain. Although only a small amount of Pex5p is bound to peroxisomes at steady state (>5%), loss of Pex13p further reduces the amount of peroxisome- associated Pex5p by approximately 40-fold. Furthermore, loss of Pex13p eliminates import of peroxisomal matrix proteins that contain either ...
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    Import of newly synthesized PTS1 proteins into the peroxisome requires the PTS1 receptor (Pex5p), a predominantly cytoplasmic protein that cycles between the cytoplasm and peroxisome. We have identified Pex13p, a novel integral peroxisomal membrane from both yeast and humans that binds the PTS1 receptor via a cytoplasmically oriented SH3 domain. Although only a small amount of Pex5p is bound to peroxisomes at steady state (>5%), loss of Pex13p further reduces the amount of peroxisome- associated Pex5p by approximately 40-fold. Furthermore, loss of Pex13p eliminates import of peroxisomal matrix proteins that contain either the type-1 or type-2 peroxisomal targeting signal but does not affect targeting and insertion of integral peroxisomal membrane proteins. We conclude that Pex13p functions as a docking factor for the predominantly cytoplasmic PTS1 receptor.
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    Journal Title
    Journal of Cell Biology
    Volume
    135
    Issue
    1
    Publisher URI
    https://rupress.org/jcb/article/135/1/85/15394/Pex13p-is-an-SH3-protein-of-the-peroxisome
    Copyright Statement
    © 1996 Rockefeller University Press. Reproduced in accordance with the copyright policy of the publisher. Use hypertext link for access to the journal's website.
    Subject
    Biological sciences
    Information and computing sciences
    Biomedical and clinical sciences
    Publication URI
    http://hdl.handle.net/10072/12606
    Collection
    • Journal articles

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