Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals-Reference-Cited by-同舟云学术

Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals

Published:2010-11-02 Issue:2 Volume:149 Page:203-210
ISSN:0021-924X
Container-title:Journal of Biochemistry
language:en
Short-container-title:Journal of Biochemistry

Author:

Honsho M.,Hashiguchi Y.,Ghaedi K.,Fujiki Y.

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,General Medicine

Link

http://academic.oup.com/jb/article-pdf/149/2/203/2494753/mvq130.pdf

Reference33 articles.

1. Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants

2. Biogenesis of Peroxisomes

3. Import of Peroxisomal Matrix and Membrane Proteins

4. Peroxisome Targeting Signal Type 1 (PTS1) Receptor Is Involved in Import of Both PTS1 and PTS2: Studies with PEX5 -Defective CHO Cell Mutants

5. The Mammalian Peroxin Pex5pL, the Longer Isoform of the Mobile Peroxisome Targeting Signal (PTS) Type 1 Transporter, Translocates the Pex7p·PTS2 Protein Complex into Peroxisomes via Its Initial Docking Site, Pex14p

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1. Peroxisome Biogenesis Disorders;Advances in Experimental Medicine and Biology;2020

2. A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform;Human Molecular Genetics;2015-07-28

3. Unique Requirements for Mono- and Polyubiquitination of the Peroxisomal Targeting Signal Co-receptor, Pex20;Journal of Biological Chemistry;2013-03

4. Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101;Biochemical Journal;2012-12-07

5. Recent advances in peroxisomal matrix protein import;Current Opinion in Cell Biology;2012-08