4iy2: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''
==Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4==
 
<StructureSection load='4iy2' size='340' side='right' caption='[[4iy2]], [[Resolution|resolution]] 3.60&Aring;' scene=''>
The entry 4iy2 is ON HOLD  until Paper Publication
== Structural highlights ==
 
<table><tr><td colspan='2'>[[4iy2]] is a 2 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=4IY2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4IY2 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>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
 
<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4iy0|4iy0]], [[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=4iy2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4iy2 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4iy2 RCSB], [http://www.ebi.ac.uk/pdbsum/4iy2 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: Cbs domain]]
[[Category: Cnnm2]]
[[Category: Cytosol]]
[[Category: Magnesium transporter]]
[[Category: Metal transport]]