| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10870328 | FEBS Letters | 2014 | 7 Pages | 
Abstract
												PEX5 acts as a cycling receptor for import of PTS1 proteins into peroxisomes and as a co-receptor for PEX7, the PTS2 receptor, but the mechanism of cargo unloading has remained obscure. Using recombinant protein domains we show PEX5 binding to the PEX14N-terminal domain (PEX14N) has no effect on the affinity of PEX5 for a PTS1 containing peptide. PEX5 can form a complex containing both recombinant PTS1 cargo and endogenous PEX7-thiolase simultaneously but isolation of the complex via the PEX14 construct resulted in an absence of thiolase, suggesting a possible role for PEX14 in the unloading of PTS2 cargos.
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											Authors
												Thomas Lanyon-Hogg, Jacob Hooper, Sarah Gunn, Stuart L. Warriner, Alison Baker, 
											