6n7e | pdb_00006n7e
From Proteopedia
Crystal structure of the cytosolic domain of human CNNM2 in complex with AMP-PNP and Mg2+
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Structural highlights
Disease[CNNM2_HUMAN] Familial primary hypomagnesemia with normocalcuria and normocalcemia. The disease is caused by mutations affecting the gene represented in this entry. Function[CNNM2_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 08:10, 4 December 2019.