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'''ATP7A''', also known as '''Menkes’ protein''' ('''MNK'''), is a copper-transporting [[P-type ATPase]] which uses the energy arising from [[ATP hydrolysis]] to transport Cu(I) across cell membranes. The ATP7A protein is a [[transmembrane protein]] and is expressed in the intestine and all tissues except liver. In the intestine, ATP7A regulates Cu(I) absorption in the human body by transporting Cu(I) from the small intestine into the blood. In other tissues, ATP7A shuttles between the [[Golgi apparatus]] and the cell membrane to maintain proper Cu(I) concentrations (since there is no free Cu(I) in the cell, Cu(I) ions are all tightly bound) in the cell and provides certain enzymes with Cu(I)(e.g. [[Peptidylglycine monooxygenase|peptidyl-α-monooxygenase]], [[tyrosinase]], and [[lysyl oxidase]]). The X-linked, inherited, lethal genetic disorder of the ''ATP7A'' gene causes [[Menkes disease]], a copper deficiency resulting in early childhood death.<ref name="pmid10079817">{{vcite2 journal | vauthors = Tümer Z, Møller LB, Horn N | title = Mutation spectrum of ATP7A, the gene defective in Menkes disease | journal = Adv. Exp. Med. Biol. | volume = 448 | issue = | pages = 83–95 | year = 1999 | pmid = 10079817 | doi = 10.1007/978-1-4615-4859-1_7 }}</ref>
== Gene ==
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