8v9u

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'''Unreleased structure'''
 
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The entry 8v9u is ON HOLD until Paper Publication
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==Solution NMR structure of human DNMT1 N-terminal alpha-helical domain==
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<StructureSection load='8v9u' size='340' side='right'caption='[[8v9u]]' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8v9u]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8V9U OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8V9U FirstGlance]. <br>
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Description:
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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[[Category: Unreleased Structures]]
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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=8v9u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8v9u OCA], [https://pdbe.org/8v9u PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8v9u RCSB], [https://www.ebi.ac.uk/pdbsum/8v9u PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8v9u ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/DNMT1_HUMAN DNMT1_HUMAN] Defects in DNMT1 are the cause of hereditary sensory neuropathy type 1E (HSN1E) [MIM:[https://omim.org/entry/614116 614116]. A neurodegenerative disorder characterized by adult onset of progressive peripheral sensory loss associated with progressive hearing impairment and early-onset dementia.<ref>PMID:21532572</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/DNMT1_HUMAN DNMT1_HUMAN] Methylates CpG residues. Preferentially methylates hemimethylated DNA. Associates with DNA replication sites in S phase maintaining the methylation pattern in the newly synthesized strand, that is essential for epigenetic inheritance. Associates with chromatin during G2 and M phases to maintain DNA methylation independently of replication. It is responsible for maintaining methylation patterns established in development. DNA methylation is coordinated with methylation of histones. Mediates transcriptional repression by direct binding to HDAC2. In association with DNMT3B and via the recruitment of CTCFL/BORIS, involved in activation of BAG1 gene expression by modulating dimethylation of promoter histone H3 at H3K4 and H3K9.<ref>PMID:16357870</ref> <ref>PMID:18754681</ref> <ref>PMID:18413740</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: Botuyan MV]]
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[[Category: Hu Q]]
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[[Category: Mer G]]

Revision as of 09:40, 1 March 2024

Solution NMR structure of human DNMT1 N-terminal alpha-helical domain

PDB ID 8v9u

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