4rwq
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Crystal structure of the apo-state of porcine OAS1== | |
- | + | <StructureSection load='4rwq' size='340' side='right'caption='[[4rwq]], [[Resolution|resolution]] 3.10Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[4rwq]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4RWQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4RWQ FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.1Å</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=4rwq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4rwq OCA], [https://pdbe.org/4rwq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4rwq RCSB], [https://www.ebi.ac.uk/pdbsum/4rwq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4rwq ProSAT]</span></td></tr> |
- | [[Category: | + | </table> |
- | [[Category: | + | == Function == |
- | [[Category: | + | [https://www.uniprot.org/uniprot/OAS1_PIG OAS1_PIG] Interferon-induced, dsRNA-activated antiviral enzyme which plays a critical role in cellular innate antiviral response. In addition, it may also play a role in other cellular processes such as apoptosis, cell growth, differentiation and gene regulation. Synthesizes higher oligomers of 2'-5'-oligoadenylates (2-5A) from ATP which then bind to the inactive monomeric form of ribonuclease L (RNase L) leading to its dimerization and subsequent activation. Activation of RNase L leads to degradation of cellular as well as viral RNA, resulting in the inhibition of protein synthesis, thus terminating viral replication. Can mediate the antiviral effect via the classical RNase L-dependent pathway or an alternative antiviral pathway independent of RNase L. The secreted form displays antiviral effect against vesicular stomatitis virus (VSV), herpes simplex virus type 2 (HSV-2), and encephalomyocarditis virus (EMCV) and stimulates the alternative antiviral pathway independent of RNase L.<ref>PMID:20844035</ref> |
- | [[Category: Fedorov | + | == References == |
- | [[Category: | + | <references/> |
- | [[Category: | + | __TOC__ |
- | [[Category: | + | </StructureSection> |
- | [[Category: Tishchenko | + | [[Category: Large Structures]] |
+ | [[Category: Sus scrofa]] | ||
+ | [[Category: Baruch P]] | ||
+ | [[Category: Fedorov R]] | ||
+ | [[Category: Kay-Fedorov P]] | ||
+ | [[Category: Lohoefener J]] | ||
+ | [[Category: Manstein DJ]] | ||
+ | [[Category: Nikulin A]] | ||
+ | [[Category: Steinke N]] | ||
+ | [[Category: Tishchenko S]] |
Current revision
Crystal structure of the apo-state of porcine OAS1
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