Cysteine Ubiquitination of PTS1 Receptor Pex5p Regulates Pex5p Recycling
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0854.2011.01217.x/fullpdf
Reference51 articles.
1. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders.;Dodt;Nat Genet,1995
2. Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.;Otera;Mol Cell Biol,1998
3. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata.;Braverman;Nat Genet,1997
4. Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor.;Motley;Nat Genet,1997
5. Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.;Purdue;Nat Genet,1997
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