4iy0
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Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4
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Structural highlights
DiseaseCNNM2_HUMAN Familial primary hypomagnesemia with normocalcuria and normocalcemia. The disease is caused by mutations affecting the gene represented in this entry. FunctionCNNM2_HUMAN Divalent metal cation transporter. Mediates transport of divalent metal cations in an order of Mg(2+) > Co(2+) > Mn(2+) > Sr(2+) > Ba(2+) > Cu(2+) > Fe(2+) (By similarity). Contents | ||||||||||||||||||||
This page was last modified 08:53, 20 March 2024.