5cyn

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'''Unreleased structure'''
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==JC Virus large T-antigen origin binding domain F258L mutant==
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<StructureSection load='5cyn' size='340' side='right' caption='[[5cyn]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
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The entry 5cyn is ON HOLD until Paper Publication
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5cyn]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5CYN OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5CYN FirstGlance]. <br>
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Authors: Meinke, G., Bohm, A., Bullock, P.A.
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr>
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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=5cyn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5cyn OCA], [http://pdbe.org/5cyn PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5cyn RCSB], [http://www.ebi.ac.uk/pdbsum/5cyn PDBsum]</span></td></tr>
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Description: JC Virus large T-antigen origin binding domain F258L mutant
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</table>
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[[Category: Unreleased Structures]]
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== Function ==
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[[Category: Bullock, P.A]]
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[[http://www.uniprot.org/uniprot/LT_POVJC LT_POVJC]] Isoform large T antigen is a key early protein essential for both driving viral replication and inducing cellular transformation. Plays a role in viral genome replication by driving entry of quiescent cells into the cell cycle and by autoregulating the synthesis of viral early mRNA. Displays highly oncogenic activities by corrupting the host cellular checkpoint mechanisms that guard cell division and the transcription, replication, and repair of DNA. Participates in the modulation of cellular gene expression preceeding viral DNA replication. This step involves binding to host key cell cycle regulators retinoblastoma protein RB1/pRb and TP53. Induces the disassembly of host E2F1 transcription factors from RB1, thus promoting transcriptional activation of E2F1-regulated S-phase genes. Inhibits host TP53 binding to DNA, abrogating the ability of TP53 to stimulate gene expression. Plays the role of a TFIID-associated factor (TAF) in transcription initiation for all three RNA polymerases, by stabilizing the TBP-TFIIA complex on promoters. Initiates viral DNA replication and unwinding via interactions with the viral origin of replication. Binds two adjacent sites in the SV40 origin. The replication fork movement is facilitated by Large T antigen helicase activity. Activates the transcription of viral late mRNA, through host TBP and TFIIA stabilization. Interferes with histone deacetylation mediated by HDAC1, leading to activation of transcription (By similarity).
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[[Category: Meinke, G]]
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__TOC__
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</StructureSection>
[[Category: Bohm, A]]
[[Category: Bohm, A]]
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[[Category: Bullock, P A]]
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[[Category: Meinke, G]]
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[[Category: Dna binding domain]]
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[[Category: Dna binding protein]]
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[[Category: Origin binding domain]]
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[[Category: Viral protein]]

Revision as of 13:57, 16 December 2015

JC Virus large T-antigen origin binding domain F258L mutant

5cyn, resolution 2.70Å

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