8hdh

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'''Unreleased structure'''
 
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The entry 8hdh is ON HOLD until 2024-11-04
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==Structure of human SGLT2-MAP17 complex with Canagliflozin==
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<StructureSection load='8hdh' size='340' side='right'caption='[[8hdh]], [[Resolution|resolution]] 3.10&Aring;' scene=''>
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Authors: Masahiro, H., Hioryuki, K., Ikuko, M., Osamu, N.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8hdh]] 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=8HDH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HDH FirstGlance]. <br>
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Description: Structure of human SGLT2-MAP17 complex with Canagliflozin
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.1&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=L3R:(2~{S},3~{R},4~{R},5~{S},6~{R})-2-[3-[[5-(4-fluorophenyl)thiophen-2-yl]methyl]-4-methyl-phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol'>L3R</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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[[Category: Hioryuki, K]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8hdh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hdh OCA], [https://pdbe.org/8hdh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hdh RCSB], [https://www.ebi.ac.uk/pdbsum/8hdh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hdh ProSAT]</span></td></tr>
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[[Category: Masahiro, H]]
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</table>
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[[Category: Ikuko, M]]
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== Disease ==
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[[Category: Osamu, N]]
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[https://www.uniprot.org/uniprot/SC5A2_HUMAN SC5A2_HUMAN] Familial renal glucosuria. The disease is caused by variants affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/SC5A2_HUMAN SC5A2_HUMAN] Electrogenic Na(+)-coupled sugar simporter that actively transports D-glucose at the plasma membrane, with a Na(+) to sugar coupling ratio of 1:1. Transporter activity is driven by a transmembrane Na(+) electrochemical gradient set by the Na(+)/K(+) pump (PubMed:20980548, PubMed:28592437, PubMed:34880493). Has a primary role in D-glucose reabsorption from glomerular filtrate across the brush border of the early proximal tubules of the kidney (By similarity).[UniProtKB:Q923I7]<ref>PMID:20980548</ref> <ref>PMID:28592437</ref> <ref>PMID:34880493</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Hioryuki K]]
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[[Category: Ikuko M]]
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[[Category: Masahiro H]]
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[[Category: Osamu N]]

Revision as of 12:00, 8 November 2023

Structure of human SGLT2-MAP17 complex with Canagliflozin

PDB ID 8hdh

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