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7wr2
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Cryatal structure of OspC3 C-terminal ankyrin-repeat domain== | |
| - | + | <StructureSection load='7wr2' size='340' side='right'caption='[[7wr2]], [[Resolution|resolution]] 1.54Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[7wr2]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Shigella_flexneri Shigella flexneri]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7WR2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7WR2 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]] 1.54Å</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=7wr2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7wr2 OCA], [https://pdbe.org/7wr2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7wr2 RCSB], [https://www.ebi.ac.uk/pdbsum/7wr2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7wr2 ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/OSPC3_SHIFL OSPC3_SHIFL] ADP-riboxanase effector that inhibits host cell pyroptosis (PubMed:23684308, PubMed:34409271, PubMed:34671164). Acts by mediating arginine ADP-riboxanation of host CASP4/CASP11, blocking CASP4/CASP11 autoprocessing (PubMed:34671164, PubMed:35338844, PubMed:35568036). This prevents CASP4 activation and ability to recognize and cleave GSDMD, thereby inhibiting LPS-induced pyroptosis (PubMed:34671164). ADP-riboxanation takes place in two steps: OspC3 first catalyzes ADP-ribosylation of target Arg, and then initiates a deamination to remove one N-omega group (PubMed:34671164). Independently of its ADP-riboxanase activity, acts as an inhibitor of calcium signaling by inhibiting host calmodulin, preventing activation of the JAK-STAT signaling pathway in response to interferon-beta (PubMed:35568036). Mechanistically, acts by binding to the apo form of calmodulin, preventing calcium-binding and ability to activate host CaMK2 (CAMKII), which is required to stimulate the JAK-STAT signaling pathway in response to interferon-beta (PubMed:35568036).<ref>PMID:23684308</ref> <ref>PMID:34409271</ref> <ref>PMID:34671164</ref> <ref>PMID:35338844</ref> <ref>PMID:35568036</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Shigella flexneri]] | ||
| + | [[Category: Ding J]] | ||
| + | [[Category: Hou YJ]] | ||
| + | [[Category: Shao F]] | ||
| + | [[Category: Zeng H]] | ||
Current revision
Cryatal structure of OspC3 C-terminal ankyrin-repeat domain
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Categories: Large Structures | Shigella flexneri | Ding J | Hou YJ | Shao F | Zeng H
