4iy4: Difference between revisions

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-{{STRUCTURE_4iy4|  PDB=4iy4  |  SCENE=  }}
-===Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4===
-==Disease==
+==Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4==
-[[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.
+<StructureSection load='4iy4' size='340' side='right'caption='[[4iy4]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
+== Structural highlights ==
-==Function==
+<table><tr><td colspan='2'>[[4iy4]] is a 2 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=4IY4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4IY4 FirstGlance]. <br>
-[[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).
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.9&#8491;</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=4iy4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4iy4 OCA], [https://pdbe.org/4iy4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4iy4 RCSB], [https://www.ebi.ac.uk/pdbsum/4iy4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4iy4 ProSAT]</span></td></tr>
-==About this Structure==
+</table>
-[[4iy4]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IY4 OCA].
+== Disease ==
-[[Category: Accardi, A.]]
+[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.
-[[Category: Corral-Rodriguez, M A.]]
+== Function ==
-[[Category: Diercks, T.]]
+[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: Encinar, J A.]]
+__TOC__
-[[Category: Ereno-Orbea, J.]]
+</StructureSection>
-[[Category: Gomez-Garcia, I.]]
+[[Category: Homo sapiens]]
-[[Category: Martinez-Cruz, L A.]]
+[[Category: Large Structures]]
-[[Category: Muller, D.]]
+[[Category: Accardi A]]
-[[Category: Oyenarte, I.]]
+[[Category: Corral-Rodriguez MA]]
-[[Category: Spiwok, V.]]
+[[Category: Diercks T]]
-[[Category: Stuiver, M.]]
+[[Category: Encinar JA]]
-[[Category: Terashima, H.]]
+[[Category: Ereno-Orbea J]]
-[[Category: Bateman domain]]
+[[Category: Gomez-Garcia I]]
-[[Category: Cbs domain]]
+[[Category: Martinez-Cruz LA]]
-[[Category: Cytosol]]
+[[Category: Muller D]]
-[[Category: Magnesium sensor]]
+[[Category: Oyenarte I]]
-[[Category: Magnesium transport]]
+[[Category: Spiwok V]]
-[[Category: Metal transport]]
+[[Category: Stuiver M]]
+[[Category: Terashima H]]