6yel: Difference between revisions
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==Stromal interaction molecule 1 coiled-coil 1 fragment== | ==Stromal interaction molecule 1 coiled-coil 1 fragment== | ||
<StructureSection load='6yel' size='340' side='right'caption='[[6yel | <StructureSection load='6yel' size='340' side='right'caption='[[6yel]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6yel]] is a 1 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6yel]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YEL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6YEL FirstGlance]. <br> | ||
</td></tr> | </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=6yel FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6yel OCA], [https://pdbe.org/6yel PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6yel RCSB], [https://www.ebi.ac.uk/pdbsum/6yel PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6yel ProSAT]</span></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/STIM1_HUMAN STIM1_HUMAN] Defects in STIM1 are the cause of immune dysfunction with T-cell inactivation due to calcium entry defect type 2 (IDTICED2) [MIM:[https://omim.org/entry/612783 612783]. IDTICED2 is an immune disorder characterized by recurrent infections, impaired T-cell activation and proliferative response, decreased T-cell production of cytokines, lymphadenopathy, and normal lymphocytes counts and serum immunoglobulin levels. Additional features include thrombocytopenia, autoimmune hemolytic anemia, non-progressive myopathy, partial iris hypoplasia, hepatosplenomegaly and defective enamel dentition.<ref>PMID:19420366</ref> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/STIM1_HUMAN STIM1_HUMAN] Plays a role in mediating store-operated Ca(2+) entry (SOCE), a Ca(2+) influx following depletion of intracellular Ca(2+) stores. Acts as Ca(2+) sensor in the endoplasmic reticulum via its EF-hand domain. Upon Ca(2+) depletion, translocates from the endoplasmic reticulum to the plasma membrane where it activates the Ca(2+) release-activated Ca(2+) (CRAC) channel subunit, TMEM142A/ORAI1.<ref>PMID:9377559</ref> <ref>PMID:16005298</ref> <ref>PMID:15866891</ref> <ref>PMID:16208375</ref> <ref>PMID:16807233</ref> <ref>PMID:16766533</ref> <ref>PMID:16733527</ref> <ref>PMID:16537481</ref> <ref>PMID:22464749</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Bechmann | [[Category: Bechmann M]] | ||
[[Category: Cerofolini | [[Category: Cerofolini L]] | ||
[[Category: Fahrner | [[Category: Fahrner M]] | ||
[[Category: Fragai | [[Category: Fragai M]] | ||
[[Category: Grabmayr | [[Category: Grabmayr H]] | ||
[[Category: Luchinat | [[Category: Luchinat C]] | ||
[[Category: Mueller | [[Category: Mueller N]] | ||
[[Category: Rathner | [[Category: Rathner P]] | ||
[[Category: Ravera | [[Category: Ravera E]] | ||
[[Category: Romanin | [[Category: Romanin C]] | ||