9jxg

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Current revision (07:16, 27 August 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9jxg is ON HOLD until Paper Publication
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==Cryo-EM structure of apo human XPR1, class 3, with symmetrically dimerized SPX domains==
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<StructureSection load='9jxg' size='340' side='right'caption='[[9jxg]], [[Resolution|resolution]] 3.75&Aring;' scene=''>
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Authors: Wang, X., Bai, Z., Wallis, C., Wang, H., Han, Y., Jin, R., Lei, M., Gu, C., Jessen, H., Shears, S., Sun, Y., Corry, B., Zhang, Y.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9jxg]] 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=9JXG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9JXG FirstGlance]. <br>
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Description: Cryo-EM structure of apo human XPR1, class 3, with symmetrically dimerized SPX domains
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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]] 3.75&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=9jxg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9jxg OCA], [https://pdbe.org/9jxg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9jxg RCSB], [https://www.ebi.ac.uk/pdbsum/9jxg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9jxg ProSAT]</span></td></tr>
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[[Category: Gu, C]]
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</table>
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[[Category: Jessen, H]]
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== Disease ==
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[[Category: Zhang, Y]]
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[https://www.uniprot.org/uniprot/S53A1_HUMAN S53A1_HUMAN] Bilateral striopallidodentate calcinosis. The disease is caused by variants affecting the gene represented in this entry.
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[[Category: Jin, R]]
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== Function ==
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[[Category: Wang, X]]
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[https://www.uniprot.org/uniprot/S53A1_HUMAN S53A1_HUMAN] Inorganic ion transporter that mediates phosphate ion export across plasma membrane. Plays a major role in phosphate homeostasis, preventing intracellular phosphate accumulation and possible calcium phosphate precipitation, ultimately preserving calcium signaling. The molecular mechanism of phosphate transport, whether electrogenic, electroneutral or coupled to other ions, remains to be elucidated (By similarity) (PubMed:23791524, PubMed:25938945, PubMed:31043717). Binds inositol hexakisphosphate (Ins6P) and similar inositol polyphosphates, such as 5-diphospho-inositol pentakisphosphate (5-InsP7), important intracellular signaling molecules involved in regulation of phosphate flux (PubMed:27080106).[UniProtKB:Q9Z0U0]<ref>PMID:23791524</ref> <ref>PMID:25938945</ref> <ref>PMID:27080106</ref> <ref>PMID:31043717</ref>
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[[Category: Lei, M]]
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== References ==
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[[Category: Bai, Z]]
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<references/>
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[[Category: Corry, B]]
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__TOC__
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[[Category: Shears, S]]
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</StructureSection>
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[[Category: Sun, Y]]
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[[Category: Homo sapiens]]
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[[Category: Wang, H]]
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[[Category: Large Structures]]
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[[Category: Wallis, C]]
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[[Category: Bai Z]]
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[[Category: Han, Y]]
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[[Category: Corry B]]
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[[Category: Gu C]]
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[[Category: Han Y]]
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[[Category: Jessen H]]
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[[Category: Jin R]]
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[[Category: Lei M]]
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[[Category: Shears S]]
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[[Category: Sun Y]]
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[[Category: Wallis C]]
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[[Category: Wang H]]
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[[Category: Wang X]]
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[[Category: Zhang Y]]

Current revision

Cryo-EM structure of apo human XPR1, class 3, with symmetrically dimerized SPX domains

PDB ID 9jxg

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