Literature summary for 7.2.2.7 extracted from

Allikmets, R.; Raskind, W.H.; Hutchinson, A.; Schueck, N.D.; Dean, M.; Koeller, D.M.
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) (1999), Hum. Mol. Genet., 8, 743-749.

Search for more literature for 7.2.2.7

Cloned(Commentary)

Cloned (Comment)	Organism
ABC7 gene	Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates	Organism	Comment (Nat. Sub.)	Natural Products	Comment (Nat. Pro.)	Rev.	Reac.
ATP + H2O + Fe3+/out	Homo sapiens	ABC7 is the causal gene of X-linked siderolastic anemia and ataxia	ADP + phosphate + Fe3+/in	-	?

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
ATP + H2O + Fe3+/out	-	Homo sapiens	ADP + phosphate + Fe3+/in	-	?
ATP + H2O + Fe3+/out	ABC7 is the causal gene of X-linked siderolastic anemia and ataxia	Homo sapiens	ADP + phosphate + Fe3+/in	-	?

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Release 2023.1 (January 2023)