3j2p
From Proteopedia
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| - | [[Image:3j2p.png|left|200px]]  | ||
| - | + | ==CryoEM structure of Dengue virus envelope protein heterotetramer==  | |
| + | <SX load='3j2p' size='340' side='right' viewer='molstar' caption='[[3j2p]], [[Resolution|resolution]] 3.60Å' scene=''>  | ||
| + | == Structural highlights ==  | ||
| + | <table><tr><td colspan='2'>[[3j2p]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Dengue_virus_2 Dengue virus 2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3J2P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3J2P FirstGlance]. <br>  | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.6Å</td></tr>  | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>  | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3j2p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3j2p OCA], [https://pdbe.org/3j2p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3j2p RCSB], [https://www.ebi.ac.uk/pdbsum/3j2p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3j2p ProSAT]</span></td></tr>  | ||
| + | </table>  | ||
| + | == Function ==  | ||
| + | [https://www.uniprot.org/uniprot/POLG_DEN2N POLG_DEN2N] Capsid protein C self-assembles to form an icosahedral capsid about 30 nm in diameter. The capsid encapsulates the genomic RNA (By similarity).  prM acts as a chaperone for envelope protein E during intracellular virion assembly by masking and inactivating envelope protein E fusion peptide. prM is matured in the last step of virion assembly, presumably to avoid catastrophic activation of the viral fusion peptide induced by the acidic pH of the trans-Golgi network. After cleavage by host furin, the pr peptide is released in the extracellular medium and small envelope protein M and envelope protein E homodimers are dissociated (By similarity).  Envelope protein E binding to host cell surface receptor is followed by virus internalization through clathrin-mediated endocytosis. Envelope protein E is subsequently involved in membrane fusion between virion and host late endosomes. Synthesized as a homodimer with prM which acts as a chaperone for envelope protein E. After cleavage of prM, envelope protein E dissociate from small envelope protein M and homodimerizes (By similarity).  Non-structural protein 1 is involved in virus replication and regulation of the innate immune response. Soluble and membrane-associated NS1 may activate human complement and induce host vascular leakage. This effect might explain the clinical manifestations of dengue hemorrhagic fever and dengue shock syndrome (By similarity).  Non-structural protein 2A may be involved viral RNA replication and capsid assembly.  Non-structural protein 2B is a required cofactor for the serine protease function of NS3.[PROSITE-ProRule:PRU00859]  Serine protease NS3 displays three enzymatic activities: serine protease, NTPase and RNA helicase. NS3 serine protease, in association with NS2B, performs its autocleavage and cleaves the polyprotein at dibasic sites in the cytoplasm: C-prM, NS2A-NS2B, NS2B-NS3, NS3-NS4A, NS4A-2K and NS4B-NS5. NS3 RNA helicase binds RNA and unwinds dsRNA in the 3' to 5' direction (By similarity).[PROSITE-ProRule:PRU00860]  Non-structural protein 4A induces host endoplasmic reticulum membrane rearrangements leading to the formation of virus-induced membranous vesicles hosting the dsRNA and polymerase, functioning as a replication complex. NS4A might also regulate the ATPase activity of the NS3 helicase (By similarity).  Peptide 2k functions as a signal peptide for NS4B and is required for the interferon antagonism activity of the latter.  Non-structural protein 4B inhibits interferon (IFN)-induced host STAT1 phosphorylation and nuclear translocation, thereby preventing the establishment of cellular antiviral state by blocking the IFN-alpha/beta pathway.  RNA-directed RNA polymerase NS5 replicates the viral (+) and (-) genome, and performs the capping of genomes in the cytoplasm. NS5 methylates viral RNA cap at guanine N-7 and ribose 2'-O positions. Besides its role in genome replication, also prevents the establishment of cellular antiviral state by blocking the interferon-alpha/beta (IFN-alpha/beta) signaling pathway. Inhibits host TYK2 and STAT2 phosphorylation, thereby preventing activation of JAK-STAT signaling pathway (By similarity).[PROSITE-ProRule:PRU00539]  | ||
| + | <div style="background-color:#fffaf0;">  | ||
| + | == Publication Abstract from PubMed ==  | ||
| + | Regulated by pH, membrane-anchored proteins E and M function during dengue virus maturation and membrane fusion. Our atomic model of the whole virion from cryo-electron microscopy at 3.5-A resolution reveals that in the mature virus at neutral extracellular pH, the N-terminal 20-amino-acid segment of M (involving three pH-sensing histidines) latches and thereby prevents spring-loaded E fusion protein from prematurely exposing its fusion peptide. This M latch is fastened at an earlier stage, during maturation at acidic pH in the trans-Golgi network. At a later stage, to initiate infection in response to acidic pH in the late endosome, M releases the latch and exposes the fusion peptide. Thus, M serves as a multistep chaperone of E to control the conformational changes accompanying maturation and infection. These pH-sensitive interactions could serve as targets for drug discovery.  | ||
| - | + | Cryo-EM structure of the mature dengue virus at 3.5-A resolution.,Zhang X, Ge P, Yu X, Brannan JM, Bi G, Zhang Q, Schein S, Zhou ZH Nat Struct Mol Biol. 2012 Dec 16. doi: 10.1038/nsmb.2463. PMID:23241927<ref>PMID:23241927</ref>  | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>  | |
| - | + | </div>  | |
| - | ==  | + | <div class="pdbe-citations 3j2p" style="background-color:#fffaf0;"></div>  | 
| - | + | == References ==  | |
| + | <references/>  | ||
| + | __TOC__  | ||
| + | </SX>  | ||
[[Category: Dengue virus 2]]  | [[Category: Dengue virus 2]]  | ||
| - | [[Category: Bi  | + | [[Category: Large Structures]]  | 
| - | [[Category: Brannan  | + | [[Category: Bi G]]  | 
| - | [[Category: Ge  | + | [[Category: Brannan JM]]  | 
| - | [[Category: Schein  | + | [[Category: Ge P]]  | 
| - | [[Category: Yu  | + | [[Category: Schein S]]  | 
| - | [[Category: Zhang  | + | [[Category: Yu X]]  | 
| - | [[Category: Zhang  | + | [[Category: Zhang Q]]  | 
| - | [[Category: Zhou  | + | [[Category: Zhang X]]  | 
| - | + | [[Category: Zhou ZH]]  | |
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Current revision
CryoEM structure of Dengue virus envelope protein heterotetramer
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Categories: Dengue virus 2 | Large Structures | Bi G | Brannan JM | Ge P | Schein S | Yu X | Zhang Q | Zhang X | Zhou ZH
