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BRENDA support

Literature summary for 7.2.2.9 extracted from

  • Lim, C.M.; Cater, M.A.; Mercer, J.F.; La Fontaine, S.
    Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A (2006), J. Biol. Chem., 281, 14006-14014.
    View publication on PubMed

Localization

Localization Comment Organism GeneOntology No. Textmining
insulin-responsive compartment ATP7B interaction with p62 is a key component of the copper-induced trafficking pathway that delivers ATP7B to subapical vesicles of hepatocytes for the removal of excess copper into bile Homo sapiens 32593
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Organism

Organism UniProt Comment Textmining
Homo sapiens P35670
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-

Source Tissue

Source Tissue Comment Organism Textmining
hepatocyte ATP7B interaction with p62 is a key component of the copper-induced trafficking pathway that delivers ATP7B to subapical vesicles of hepatocytes for the removal of excess copper into bile Homo sapiens
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skin fibroblast
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Homo sapiens
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Synonyms

Synonyms Comment Organism
ATP7B
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Homo sapiens