1wh3
From Proteopedia
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<StructureSection load='1wh3' size='340' side='right'caption='[[1wh3]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | <StructureSection load='1wh3' size='340' side='right'caption='[[1wh3]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[1wh3]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[1wh3]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WH3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1WH3 FirstGlance]. <br> |
- | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">IMS cDNA adSE00628 ([ | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">IMS cDNA adSE00628 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1wh3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wh3 OCA], [https://pdbe.org/1wh3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1wh3 RCSB], [https://www.ebi.ac.uk/pdbsum/1wh3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1wh3 ProSAT], [https://www.topsan.org/Proteins/RSGI/1wh3 TOPSAN]</span></td></tr> |
</table> | </table> | ||
== Function == | == Function == | ||
- | [[ | + | [[https://www.uniprot.org/uniprot/OASL_HUMAN OASL_HUMAN]] Does not have 2'-5'-OAS activity, but can bind double-stranded RNA. Displays antiviral activity against encephalomyocarditis virus (EMCV) and hepatitis C virus (HCV) via an alternative antiviral pathway independent of RNase L.<ref>PMID:9826176</ref> <ref>PMID:18931074</ref> <ref>PMID:20074559</ref> |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] |
Revision as of 06:54, 2 March 2022
Solution structure of C-terminal ubiquitin like domain of human 2'-5'-oligoadenylate synthetase-like protain (p59 OASL)
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Categories: Human | Large Structures | Inoue, M | Kigawa, T | Koshiba, S | Structural genomic | Tochio, N | Tomizawa, T | Yokoyama, S | P59 oasl | Protein binding | Rsgi | Ubiquitin family