8vud

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Current revision (05:31, 30 July 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8vud is ON HOLD until Paper Publication
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==Crystal structure of APOBEC3F-CD1==
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<StructureSection load='8vud' size='340' side='right'caption='[[8vud]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
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Authors: Yang, H.J., Li, S.-X., Pacheco, J., Chen, X.S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8vud]] 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=8VUD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8VUD FirstGlance]. <br>
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Description: Crystal structure of APOBEC3F-CD1
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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]] 2.599&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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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[[Category: Li, S.-X]]
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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=8vud FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8vud OCA], [https://pdbe.org/8vud PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8vud RCSB], [https://www.ebi.ac.uk/pdbsum/8vud PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8vud ProSAT]</span></td></tr>
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[[Category: Yang, H.J]]
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</table>
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[[Category: Pacheco, J]]
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== Function ==
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[[Category: Chen, X.S]]
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[https://www.uniprot.org/uniprot/ABC3F_HUMAN ABC3F_HUMAN] DNA deaminase (cytidine deaminase) which acts as an inhibitor of retrovirus replication and retrotransposon mobility via deaminase-dependent and -independent mechanisms. Exhibits antiviral activity against vif-deficient HIV-1. After the penetration of retroviral nucleocapsids into target cells of infection and the initiation of reverse transcription, it can induce the conversion of cytosine to uracil in the minus-sense single-strand viral DNA, leading to G-to-A hypermutations in the subsequent plus-strand viral DNA. The resultant detrimental levels of mutations in the proviral genome, along with a deamination-independent mechanism that works prior to the proviral integration, together exert efficient antiretroviral effects in infected target cells. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single- or double-stranded RNA. Exhibits antiviral activity also against hepatitis B virus (HBV), equine infectious anemia virus (EIAV), xenotropic MuLV-related virus (XMRV) and simian foamy virus (SFV) and may inhibit the mobility of LTR and non-LTR retrotransposons. May also play a role in the epigenetic regulation of gene expression through the process of active DNA demethylation.<ref>PMID:15152192</ref> <ref>PMID:16527742</ref> <ref>PMID:16378963</ref> <ref>PMID:19458006</ref> <ref>PMID:20219927</ref> <ref>PMID:20335265</ref> <ref>PMID:20062055</ref> <ref>PMID:21496894</ref> <ref>PMID:21835787</ref> <ref>PMID:22915799</ref> <ref>PMID:22807680</ref> <ref>PMID:23097438</ref> <ref>PMID:23152537</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: Chen XS]]
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[[Category: Li S-X]]
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[[Category: Pacheco J]]
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[[Category: Yang HJ]]

Current revision

Crystal structure of APOBEC3F-CD1

PDB ID 8vud

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