4iy0

<StructureSection load='4iy0' size='340' side='right'caption='[[4iy0]], [[Resolution|resolution]] 1.90&Aring;' scene=''>

<table><tr><td colspan='2'>[[4iy0]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IY0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4IY0 FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=ADP:ADENOSINE-5-DIPHOSPHATE'>ADP</scene></td></tr>

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4iy0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4iy0 OCA], [https://pdbe.org/4iy0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4iy0 RCSB], [https://www.ebi.ac.uk/pdbsum/4iy0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4iy0 ProSAT]</span></td></tr>

[https://www.uniprot.org/uniprot/CNNM2_HUMAN CNNM2_HUMAN] Familial primary hypomagnesemia with normocalcuria and normocalcemia. The disease is caused by mutations affecting the gene represented in this entry.

[https://www.uniprot.org/uniprot/CNNM2_HUMAN 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).

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Accardi A]]

[[Category: Corral-Rodriguez MA]]

[[Category: Diercks T]]

[[Category: Encinar JA]]

[[Category: Ereno-Orbea J]]

[[Category: Gomez-Garcia I]]

[[Category: Martinez-Cruz LA]]

[[Category: Muller D]]

[[Category: Oyenarte I]]

[[Category: Spiwok V]]

[[Category: Stuiver M]]

[[Category: Terashima H]]