8ex7
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Human S1P transporter Spns2 in an outward-facing partially occluded conformation (state 3)== | |
- | + | <StructureSection load='8ex7' size='340' side='right'caption='[[8ex7]], [[Resolution|resolution]] 3.53Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8ex7]] is a 1 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=8EX7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8EX7 FirstGlance]. <br> | |
- | + | </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=8ex7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ex7 OCA], [https://pdbe.org/8ex7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ex7 RCSB], [https://www.ebi.ac.uk/pdbsum/8ex7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ex7 ProSAT]</span></td></tr> | |
- | [[Category: | + | </table> |
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/SPNS2_HUMAN SPNS2_HUMAN] The disease is caused by variants affecting the gene represented in this entry. | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/SPNS2_HUMAN SPNS2_HUMAN] Lipid transporter that specifically mediates export of sphingosine-1-phosphate (sphing-4-enine 1-phosphate, S1P) and sphinganine-1-phosphate in the lymph, thereby playing a role in lymphocyte trafficking (PubMed:19074308, PubMed:23180825, PubMed:21084291). S1P is a bioactive signaling molecule that regulates many physiological processes important for the development and for the immune system (PubMed:19074308, PubMed:23180825). Regulates levels of S1P and the S1P gradient that exists between the high circulating concentrations of S1P and low tissue levels that control lymphocyte trafficking (PubMed:19074308, PubMed:23180825). Required for the egress of T-cells from lymph nodes during an immune response by mediating S1P secretion, which generates a gradient that enables activated T-cells to access lymph (By similarity). Also required for the egress of immature B-cells from the bone marrow (By similarity). In contrast, not involved in S1P release from red blood cells (By similarity). Involved in auditory function (PubMed:30973865). S1P release in the inner ear is required for maintenance of the endocochlear potential in the cochlea (By similarity). In addition to export, also able to mediate S1P import (By similarity).[UniProtKB:Q91VM4]<ref>PMID:19074308</ref> <ref>PMID:21084291</ref> <ref>PMID:23180825</ref> <ref>PMID:30973865</ref> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Ahmed S]] | ||
+ | [[Category: Dai Y]] | ||
+ | [[Category: Lee CH]] | ||
+ | [[Category: Zhao H]] |
Revision as of 05:42, 31 May 2023
Human S1P transporter Spns2 in an outward-facing partially occluded conformation (state 3)
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Categories: Homo sapiens | Large Structures | Ahmed S | Dai Y | Lee CH | Zhao H