Iron-sulfur clusters transporter ABCB7, mitochondrial
Definition:
References:
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[1]. R Allikmets, et al. Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Hum Mol Genet. 1999 May;8(5):743-9. [Content Brief]
[2]. Patrizia Cavadini, et al. RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload. Blood. 2007 Apr 15;109(8):3552-9. [Content Brief]
[3]. Nunziata Maio, et al. Dimeric ferrochelatase bridges ABCB7 and ABCB10 homodimers in an architecturally defined molecular complex required for heme biosynthesis. Haematologica. 2019 Sep;104(9):1756-1767. [Content Brief]
[4]. Stephen A Pearson, et al. Evolution of the human mitochondrial ABCB7 [2Fe-2S](GS)4 cluster exporter and the molecular mechanism of an E433K disease-causing mutation. Arch Biochem Biophys. 2021 Jan 15;697:108661. [Content Brief]
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