4iy0: Difference between revisions

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-'''Unreleased structure'''
+==Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4==
+<StructureSection load='4iy0' size='340' side='right' caption='[[4iy0]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
-The entry 4iy0 is ON HOLD  until Paper Publication
+== Structural highlights ==
+<table><tr><td colspan='2'>[[4iy0]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. 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 [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4IY0 FirstGlance]. <br>
-Authors: Corral-Rodriguez, M.A., Stuiver, M., Encinar, J.A., Spiwok, V., Gomez-Garcia, I., Oyenarte, I., Ereno-Orbea, J., Terashima, H., Accardi, A., Diercks, T., Muller, D., Martinez-Cruz, L.A.
+</td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=ADP:ADENOSINE-5-DIPHOSPHATE'>ADP</scene><br>
+<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4iy2|4iy2]], [[4iy3|4iy3]], [[4iy4|4iy4]]</td></tr>
-Description: Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4
+<tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CNNM2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
+<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4iy0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4iy0 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4iy0 RCSB], [http://www.ebi.ac.uk/pdbsum/4iy0 PDBsum]</span></td></tr>
+<table>
+== Disease ==
+[[http://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.
+== Function ==
+[[http://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).
+__TOC__
+</StructureSection>
+[[Category: Human]]
+[[Category: Accardi, A.]]
+[[Category: Corral-Rodriguez, M A.]]
+[[Category: Diercks, T.]]
+[[Category: Encinar, J A.]]
+[[Category: Ereno-Orbea, J.]]
+[[Category: Gomez-Garcia, I.]]
+[[Category: Martinez-Cruz, L A.]]
+[[Category: Muller, D.]]
+[[Category: Oyenarte, I.]]
+[[Category: Spiwok, V.]]
+[[Category: Stuiver, M.]]
+[[Category: Terashima, H.]]
+[[Category: Bateman domain]]
+[[Category: Cb]]
+[[Category: Cytosol]]
+[[Category: Magnesium sensor]]
+[[Category: Magnesium transporter]]
+[[Category: Metal transport]]