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| http://purl.uniprot.org/citations/26453804 | http://www.w3.org/2000/01/rdf-schema#comment | "Mutations in the PEX1 gene, which encodes a protein required for peroxisome biogenesis, are the most common cause of the Zellweger spectrum diseases. The recognition that Pex1p shares a conserved ATP-binding domain with p97 and NSF led to the discovery of the extended family of AAA+-type ATPases. So far, four AAA+-type ATPases are related to peroxisome function. Pex6p functions together with Pex1p in peroxisome biogenesis, ATAD1/Msp1p plays a role in membrane protein targeting and a member of the Lon-family of proteases is associated with peroxisomal quality control. This review summarizes the current knowledge on the AAA+-proteins involved in peroxisome biogenesis and function."xsd:string |
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| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/author | "Erdmann R."xsd:string |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/author | "Girzalsky W."xsd:string |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/author | "Grimm I."xsd:string |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/date | "2016"xsd:gYear |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/name | "Biochim Biophys Acta"xsd:string |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/pages | "828-837"xsd:string |
| http://purl.uniprot.org/citations/26453804 | http://purl.uniprot.org/core/title | "Role of AAA(+)-proteins in peroxisome biogenesis and function."xsd:string |
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