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8hb0

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Current revision (13:08, 1 November 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8hb0 is ON HOLD until 2024-10-27
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==Structure of human SGLT2-MAP17 complex with TA1887==
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<StructureSection load='8hb0' size='340' side='right'caption='[[8hb0]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
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Authors: Hiraizumi, M., Kishida, H., Miyaguchi, I., Nureki, O.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8hb0]] 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=8HB0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HB0 FirstGlance]. <br>
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Description: Structure of human SGLT2-MAP17 complex with TA1887
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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]] 2.9&#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=KZ3:(2R,3R,4S,5S,6R)-2-[3-[(4-cyclopropylphenyl)methyl]-4-fluoranyl-indol-1-yl]-6-(hydroxymethyl)oxane-3,4,5-triol'>KZ3</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: Nureki, O]]
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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=8hb0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hb0 OCA], [https://pdbe.org/8hb0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hb0 RCSB], [https://www.ebi.ac.uk/pdbsum/8hb0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hb0 ProSAT]</span></td></tr>
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[[Category: Kishida, H]]
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</table>
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[[Category: Miyaguchi, I]]
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== Disease ==
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[[Category: Hiraizumi, M]]
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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: Hiraizumi M]]
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[[Category: Kishida H]]
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[[Category: Miyaguchi I]]
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[[Category: Nureki O]]

Current revision

Structure of human SGLT2-MAP17 complex with TA1887

PDB ID 8hb0

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