View source for 9ywq


==the structure of ERMA complex with ATPrS and Mg++==
<StructureSection load='9ywq' size='340' side='right'caption='[[9ywq]], [[Resolution|resolution]] 3.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9ywq]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9YWQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9YWQ FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AGS:PHOSPHOTHIOPHOSPHORIC+ACID-ADENYLATE+ESTER'>AGS</scene>, <scene name='pdbligand=D10:DECANE'>D10</scene>, <scene name='pdbligand=D12:DODECANE'>D12</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=OCT:N-OCTANE'>OCT</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=9ywq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ywq OCA], [https://pdbe.org/9ywq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ywq RCSB], [https://www.ebi.ac.uk/pdbsum/9ywq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ywq ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/TMM94_MOUSE TMM94_MOUSE] Could function in the uptake of Mg(2+) from the cytosol into the endoplasmic reticulum and regulate intracellular Mg(2+) homeostasis.<ref>PMID:38513662</ref> 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Magnesium (Mg(2+)) is the most abundant divalent cation in cells, yet the mechanisms mediating its organellar transport remain poorly defined. We identify endoplasmic reticulum (ER) Mg(2+) adenosine triphosphatase (ATPase) (ERMA) as the transporter that drives Mg(2+) uptake into the ER lumen, establishing the ER as a bi-ionic intracellular reservoir. MagFRET biosensors targeted to the ER demonstrate that ERMA mediates dynamic ER Mg(2+) storage and robust adenosine 5'-triphosphate-dependent Mg(2+) uptake reaching 15 to 30 millimolar. Cryo-electron microscopy structures of human and mouse ERMA reveal a P-type ATPase fold with an unwound transmembrane 4 (TM4) that coordinates Mg(2+) via the unique PILP backbone and the TM5 residue Q1110, whose mutation markedly impairs ERMA-mediated Mg(2+) uptake. Functional reconstitution of domain mutants, ERMA-SERCA chimeras, and pathogenic variants confirm ERMA as an ER-resident Mg(2+) pump and gatekeeper of ER Mg(2+) ionic equilibrium.

Structural and mutational insights define ERMA as the ER Mg(2+) ATPase and reservoir gatekeeper.,Venkatesan M, Oldham ML, Shi N, Chidambaram A, Vishnu N, Madesh AK, Bentz K, Stathopulos PB, Kalathur RC, Jiang Y, Madesh M Sci Adv. 2026 Jul 3;12(27):eaef4971. doi: 10.1126/sciadv.aef4971. Epub 2026 Jul , 1. PMID:42384784<ref>PMID:42384784</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 9ywq" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Jiang Y]]
[[Category: Shi N]]