7z0j
From Proteopedia
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== Disease == | == Disease == | ||
| - | [https://www.uniprot.org/uniprot/PEX13_HUMAN PEX13_HUMAN] | + | [https://www.uniprot.org/uniprot/PEX13_HUMAN PEX13_HUMAN] Neonatal adrenoleukodystrophy;Infantile Refsum disease;Zellweger syndrome. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. |
== Function == | == Function == | ||
| - | [https://www.uniprot.org/uniprot/PEX13_HUMAN PEX13_HUMAN] Component of the PEX13-PEX14 docking complex, a translocon channel that specifically mediates the import of peroxisomal cargo proteins bound to PEX5 receptor (PubMed: | + | [https://www.uniprot.org/uniprot/PEX13_HUMAN PEX13_HUMAN] Component of the PEX13-PEX14 docking complex, a translocon channel that specifically mediates the import of peroxisomal cargo proteins bound to PEX5 receptor (PubMed:28765278, PubMed:8858165, PubMed:9653144). The PEX13-PEX14 docking complex forms a large import pore which can be opened to a diameter of about 9 nm (By similarity). Mechanistically, PEX5 receptor along with cargo proteins associates with the PEX14 subunit of the PEX13-PEX14 docking complex in the cytosol, leading to the insertion of the receptor into the organelle membrane with the concomitant translocation of the cargo into the peroxisome matrix (PubMed:28765278, PubMed:8858165, PubMed:9653144). Involved in the import of PTS1- and PTS2-type containing proteins (PubMed:8858165, PubMed:9653144).[UniProtKB:P80667]<ref>PMID:28765278</ref> <ref>PMID:8858165</ref> <ref>PMID:9653144</ref> |
== References == | == References == | ||
<references/> | <references/> | ||
Current revision
human PEX13 SH3 domain in complex with internal FxxxF motif
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