1n6g

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(New page: 200px<br /><applet load="1n6g" size="450" color="white" frame="true" align="right" spinBox="true" caption="1n6g" /> '''The structure of immature Dengue-2 prM parti...)
Current revision (07:53, 14 February 2024) (edit) (undo)
 
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[[Image:1n6g.gif|left|200px]]<br /><applet load="1n6g" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1n6g" />
 
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'''The structure of immature Dengue-2 prM particles'''<br />
 
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==Overview==
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==The structure of immature Dengue-2 prM particles==
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Structures of prM-containing dengue and yellow fever virus particles were, determined to 16 and 25 A resolution, respectively, by cryoelectron, microscopy and image reconstruction techniques. The closely similar, structures show 60 icosahedrally organized trimeric spikes on the particle, surface. Each spike consists of three prM:E heterodimers, where E is an, envelope glycoprotein and prM is the precursor to the membrane protein M., The pre-peptide components of the prM proteins in each spike cover the, fusion peptides at the distal ends of the E glycoproteins in a manner, similar to the organization of the glycoproteins in the alphavirus spikes., Each heterodimer is associated with an E and a prM transmembrane density., These transmembrane densities represent either an EE or prMprM, antiparallel coiled coil by which each protein spans the membrane twice, leaving the C-terminus of each protein on the exterior of the viral, membrane, consistent with the predicted membrane-spanning domains of the, unprocessed polyprotein.
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<SX load='1n6g' size='340' side='right' viewer='molstar' caption='[[1n6g]], [[Resolution|resolution]] 16.00&Aring;' scene=''>
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== Structural highlights ==
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==About this Structure==
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<table><tr><td colspan='2'>[[1n6g]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Dengue_virus_2_Puerto_Rico/PR159-S1/1969 Dengue virus 2 Puerto Rico/PR159-S1/1969]. The July 2008 RCSB PDB [https://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/index.html Molecule of the Month] feature on ''Dengue Virus'' by David Goodsell is [https://dx.doi.org/10.2210/rcsb_pdb/mom_2008_7 10.2210/rcsb_pdb/mom_2008_7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1N6G OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1N6G FirstGlance]. <br>
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1N6G is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Dengue_virus_type_3 Dengue virus type 3]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1N6G OCA].
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 16&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1n6g FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1n6g OCA], [https://pdbe.org/1n6g PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1n6g RCSB], [https://www.ebi.ac.uk/pdbsum/1n6g PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1n6g ProSAT]</span></td></tr>
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==Reference==
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</table>
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Structures of immature flavivirus particles., Zhang Y, Corver J, Chipman PR, Zhang W, Pletnev SV, Sedlak D, Baker TS, Strauss JH, Kuhn RJ, Rossmann MG, EMBO J. 2003 Jun 2;22(11):2604-13. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12773377 12773377]
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== Function ==
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[[Category: Dengue virus type 3]]
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[https://www.uniprot.org/uniprot/POLG_TBEVW POLG_TBEVW] 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 (By similarity). Non-structural protein 2A may be involved viral RNA replication and capsid assembly (Potential). Non-structural protein 2B is a required cofactor for the serine protease function of NS3 (By similarity). 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). 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 (By similarity). 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 SCRIB and prevents activation of downstream JAK-STAT signaling pathway (By similarity).
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[[Category: Single protein]]
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== Evolutionary Conservation ==
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[[Category: Baker, T.S.]]
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[[Image:Consurf_key_small.gif|200px|right]]
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[[Category: Chipman, P.R.]]
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Check<jmol>
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[[Category: Corver, J.]]
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<jmolCheckbox>
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[[Category: Kuhn, R.J.]]
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/n6/1n6g_consurf.spt"</scriptWhenChecked>
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[[Category: Pletnev, S.V.]]
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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[[Category: Rossmann, M.G.]]
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<text>to colour the structure by Evolutionary Conservation</text>
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[[Category: Sedlak, D.]]
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</jmolCheckbox>
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[[Category: Strauss, J.H.]]
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1n6g ConSurf].
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[[Category: Zhang, W.]]
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<div style="clear:both"></div>
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[[Category: Zhang, Y.]]
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__TOC__
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[[Category: dengue immature virus]]
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</SX>
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[[Category: flaviviridae]]
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[[Category: Dengue Virus]]
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[[Category: flavivirus]]
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[[Category: Dengue virus 2 Puerto Rico/PR159-S1/1969]]
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[[Category: icosahedral virus]]
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[[Category: Large Structures]]
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[[Category: prm particle]]
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[[Category: RCSB PDB Molecule of the Month]]
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[[Category: Baker TS]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:00:13 2007''
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[[Category: Chipman PR]]
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[[Category: Corver J]]
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[[Category: Kuhn RJ]]
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[[Category: Pletnev SV]]
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[[Category: Rossmann MG]]
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[[Category: Sedlak D]]
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[[Category: Strauss JH]]
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[[Category: Zhang W]]
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[[Category: Zhang Y]]

Current revision

The structure of immature Dengue-2 prM particles

1n6g, resolution 16.00Å

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