3teq: Difference between revisions
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{{STRUCTURE_3teq| PDB=3teq | SCENE= }} | {{STRUCTURE_3teq| PDB=3teq | SCENE= }} | ||
===Crystal structure of SOAR domain=== | ===Crystal structure of SOAR domain=== | ||
{{ABSTRACT_PUBMED_22451904}} | |||
==Disease== | |||
[[http://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:[http://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== | |||
[[http://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> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:022451904</ref><references group="xtra"/> | <ref group="xtra">PMID:022451904</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Cai, X.]] | [[Category: Cai, X.]] |