8deh

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'''Unreleased structure'''
 
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The entry 8deh is ON HOLD until Paper Publication
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==Ankyrin domain of SKD3==
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<StructureSection load='8deh' size='340' side='right'caption='[[8deh]], [[Resolution|resolution]] 1.81&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8deh]] 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=8DEH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8DEH FirstGlance]. <br>
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Description:
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</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=8deh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8deh OCA], [https://pdbe.org/8deh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8deh RCSB], [https://www.ebi.ac.uk/pdbsum/8deh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8deh ProSAT]</span></td></tr>
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[[Category: Unreleased Structures]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/CLPB_HUMAN CLPB_HUMAN] 3-methylglutaconic aciduria type 7;Autosomal dominant severe congenital neutropenia. 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/CLPB_HUMAN CLPB_HUMAN] May function as a regulatory ATPase and be related to secretion/protein trafficking process. Involved in mitochondrial-mediated antiviral innate immunity, activates RIG-I-mediated signal transduction and production of IFNB1 and pro-inflammatory cytokine IL6 (PubMed:31522117).<ref>PMID:31522117</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: Lee S]]
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[[Category: Tsai FTF]]

Revision as of 09:26, 19 April 2023

Ankyrin domain of SKD3

PDB ID 8deh

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