8f6d
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Crystal structure of the CNNM2 CBS-pair domain in complex with ARL15
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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 07:20, 12 July 2023.