4rov

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m (Protected "4rov" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 4rov is ON HOLD
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==The crystal structure of novel APOBEC3G CD2 head-to-tail dimer suggests the binding mode of full-length APOBEC3G to HIV-1 ssDNA==
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<StructureSection load='4rov' size='340' side='right'caption='[[4rov]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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Authors: Xiuxiu Lu, Tianlong Zhang, Zeng Xu, Shanshan Liu, Bin Zhao, Wenxian Lan, Chunxi Wang, Jianping Ding, Chunyang Cao, Midwest Center for Structural Genomics (MCSG)
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4rov]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ROV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4ROV FirstGlance]. <br>
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Description: The crystal structure of novel APOBEC3G CD2 head-to-tail dimer suggests the binding mode of full-length APOBEC3G to HIV-1 ssDNA
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=4rov FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4rov OCA], [https://pdbe.org/4rov PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4rov RCSB], [https://www.ebi.ac.uk/pdbsum/4rov PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4rov ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/ABC3G_HUMAN ABC3G_HUMAN] DNA deaminase (cytidine deaminase) that mediates a form of innate resistance to retroviral infections (at least to HIV-1 infection) by triggering G-to-A hypermutation in the newly synthesized viral DNA. The replacements C-to-U in the minus strand DNA of HIV-1 during reverse transcription, leads to G-to-A transitions in the plus strand. The inhibition of viral replication is either due to the degradation of the minus strand before its integration or to the lethality of the hypermutations. Modification of both DNA strands is not excluded. This antiviral activity is neutralized by the virion infectivity factor (VIF), that prevents the incorporation of APOBEC3G into progeny HIV-1 virions by both inhibiting its translation and/or by inducing its ubiquitination and subsequent degradation by the 26S proteasome. May also prevent the transposition of a subset of retroelements. Binds a variety of RNAs, but does not display detectable APOB, NF1 and NAT1 mRNA editing.<ref>PMID:14557625</ref> <ref>PMID:12167863</ref> <ref>PMID:12808466</ref> <ref>PMID:12809610</ref> <ref>PMID:12808465</ref> <ref>PMID:12859895</ref> <ref>PMID:12970355</ref> <ref>PMID:14528300</ref> <ref>PMID:15031497</ref> <ref>PMID:16527742</ref> <ref>PMID:21123384</ref> <ref>PMID:18288108</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: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Cao C]]
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[[Category: Ding J]]
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[[Category: Lan W]]
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[[Category: Liu S]]
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[[Category: Lu X]]
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[[Category: Wang C]]
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[[Category: Xu Z]]
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[[Category: Zhang T]]
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[[Category: Zhao B]]

Current revision

The crystal structure of novel APOBEC3G CD2 head-to-tail dimer suggests the binding mode of full-length APOBEC3G to HIV-1 ssDNA

PDB ID 4rov

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