6twu

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m (Protected "6twu" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6twu is ON HOLD until Paper Publication
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==MAGI1_2 complexed with a phosphomimetic 16E6 peptide==
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<StructureSection load='6twu' size='340' side='right'caption='[[6twu]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
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Authors: Gogl, G., Cousido-Siah, A., Trave, G.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6twu]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6TWU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6TWU FirstGlance]. <br>
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Description: MAGI1_2 complexed with a phosphomimetic 16E6 peptide
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CIT:CITRIC+ACID'>CIT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6twu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6twu OCA], [http://pdbe.org/6twu PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6twu RCSB], [http://www.ebi.ac.uk/pdbsum/6twu PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6twu ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/MAGI1_HUMAN MAGI1_HUMAN]] May play a role as scaffolding protein at cell-cell junctions. May regulate acid-induced ASIC3 currents by modulating its expression at the cell surface (By similarity). [[http://www.uniprot.org/uniprot/VE6_HPV16 VE6_HPV16]] Plays a major role in the induction and maintenance of cellular transformation. Acts mainly as an oncoprotein by stimulating the destruction of many host cell key regulatory proteins. E6 associates with host E6-AP ubiquitin-protein ligase, and inactivates tumor suppressors TP53 and TP73 by targeting them to the 26S proteasome for degradation. In turn, DNA damage and chromosomal instabilities increase and lead to cell proliferation and cancer development. The complex E6/E6P targets several other substrates to degradation via the proteasome including host NFX1-91, a repressor of human telomerase reverse transcriptase (hTERT). The resulting increased expression of hTERT prevents the shortening of telomere length leading to cell immortalization. Other cellular targets including Bak, Fas-associated death domain-containing protein (FADD) and procaspase 8, are degraded by E6/E6AP causing inhibition of apoptosis. E6 also inhibits immune response by interacting with host IRF3 and TYK2. These interactions prevent IRF3 transcriptional activities and inhibit TYK2-mediated JAK-STAT activation by interferon alpha resulting in inhibition of the interferon signaling pathway.<ref>PMID:8598912</ref> <ref>PMID:9649509</ref> <ref>PMID:10523853</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: Large Structures]]
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[[Category: Cousido-Siah, A]]
[[Category: Gogl, G]]
[[Category: Gogl, G]]
[[Category: Trave, G]]
[[Category: Trave, G]]
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[[Category: Cousido-Siah, A]]
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[[Category: Motif]]
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[[Category: Pdz domain]]
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[[Category: Peptide binding protein]]
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[[Category: Phosphorylation]]

Revision as of 09:22, 1 April 2020

MAGI1_2 complexed with a phosphomimetic 16E6 peptide

PDB ID 6twu

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