8y4z
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Monomeric HERC5 HECT c-lobe structure in solution== | |
- | + | <StructureSection load='8y4z' size='340' side='right'caption='[[8y4z]]' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8y4z]] 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=8Y4Z OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8Y4Z FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> | |
- | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8y4z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8y4z OCA], [https://pdbe.org/8y4z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8y4z RCSB], [https://www.ebi.ac.uk/pdbsum/8y4z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8y4z ProSAT]</span></td></tr> |
- | [[Category: | + | </table> |
- | [[Category: | + | == Function == |
- | [[Category: | + | [https://www.uniprot.org/uniprot/HERC5_HUMAN HERC5_HUMAN] Major E3 ligase for ISG15 conjugation (PubMed:26355087, PubMed:27564865, PubMed:27534820, PubMed:34572049, PubMed:37279284). Acts as a positive regulator of innate antiviral response in cells induced by interferon. Functions as part of the ISGylation machinery that recognizes target proteins in a broad and relatively non-specific manner. Catalyzes ISGylation of IRF3 which results in sustained activation, it attenuates IRF3-PIN1 interaction, which antagonizes IRF3 ubiquitination and degradation, and boosts the antiviral response. Mediates ISGylation of the phosphatase PTEN leading to its degradation, thus alleviating its suppression of the PI3K-AKT signaling pathway and promoting the production of cytokines that facilitate bacterial clearance (PubMed:37279284). Interferes with the function of key viral structural proteins such as ebolavirus structural protein VP40 or HIV-1 protein GAG (PubMed:22093708, PubMed:34572049). Catalyzes ISGylation of influenza A viral NS1 which attenuates virulence; ISGylated NS1 fails to form homodimers and thus to interact with its RNA targets. Catalyzes ISGylation of papillomavirus type 16 L1 protein which results in dominant-negative effect on virus infectivity. Physically associated with polyribosomes, broadly modifies newly synthesized proteins in a cotranslational manner. In an interferon-stimulated cell, newly translated viral proteins are primary targets of ISG15. Promotes parkin/PRKN ubiquitin E3 ligase activity by suppressing the intramolecular interaction that maintains its autoinhibited conformation (PubMed:27534820).<ref>PMID:16407192</ref> <ref>PMID:16815975</ref> <ref>PMID:16884686</ref> <ref>PMID:20133869</ref> <ref>PMID:20308324</ref> <ref>PMID:20385878</ref> <ref>PMID:20542004</ref> <ref>PMID:22093708</ref> <ref>PMID:26355087</ref> <ref>PMID:27534820</ref> <ref>PMID:27564865</ref> <ref>PMID:34572049</ref> <ref>PMID:37279284</ref> (Microbial infection) Functions as an E3 ligase for ISGylation of hepatitis B virus protein X leading to enhanced viral replication due to increased interferon resistance.<ref>PMID:34661519</ref> |
- | [[Category: | + | == References == |
- | [[Category: | + | <references/> |
- | [[Category: Lambert | + | __TOC__ |
- | [[Category: | + | </StructureSection> |
- | [[Category: | + | [[Category: Homo sapiens]] |
+ | [[Category: Large Structures]] | ||
+ | [[Category: Dag C]] | ||
+ | [[Category: Dotsch V]] | ||
+ | [[Category: Gocenler O]] | ||
+ | [[Category: Guntert P]] | ||
+ | [[Category: Kahraman K]] | ||
+ | [[Category: Lambert M]] | ||
+ | [[Category: Lee W]] | ||
+ | [[Category: Lohn F]] |
Current revision
Monomeric HERC5 HECT c-lobe structure in solution
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Categories: Homo sapiens | Large Structures | Dag C | Dotsch V | Gocenler O | Guntert P | Kahraman K | Lambert M | Lee W | Lohn F