8q1n

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m (Protected "8q1n" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 8q1n is ON HOLD
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==Cyclic peptide binder of the WBM-site of WDR5==
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<StructureSection load='8q1n' size='340' side='right'caption='[[8q1n]], [[Resolution|resolution]] 1.84&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8q1n]] is a 4 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=8Q1N OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8Q1N FirstGlance]. <br>
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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]] 1.843&#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=DAB:2,4-DIAMINOBUTYRIC+ACID'>DAB</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=8q1n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8q1n OCA], [https://pdbe.org/8q1n PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8q1n RCSB], [https://www.ebi.ac.uk/pdbsum/8q1n PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8q1n ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/WDR5_HUMAN WDR5_HUMAN] Contributes to histone modification. May position the N-terminus of histone H3 for efficient trimethylation at 'Lys-4'. As part of the MLL1/MLL complex it is involved in methylation and dimethylation at 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. As part of the NSL complex it may be involved in acetylation of nucleosomal histone H4 on several lysine residues. May regulate osteoblasts differentiation.<ref>PMID:19556245</ref> <ref>PMID:19103755</ref> <ref>PMID:20018852</ref> <ref>PMID:16600877</ref> <ref>PMID:16829960</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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WDR5 is an adaptor protein involved in the regulation of various epigenetic modifier complexes. Various inhibitors have been described but only as inhibitors of its protein-protein interactions. Here we describe peptidic macrocycles that act as inhibitors of the interaction between WDR5 and long non-coding RNAs. The findings provide a new strategy to modulate the biological function of WDR5 as an RNA binding epigenetic regulator.
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Authors:
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Macrocyclic peptides as inhibitors of WDR5-lncRNA interactions.,Chang JY, Neugebauer C, Schmeing S, Amrahova G, 't Hart P Chem Commun (Camb). 2023 Aug 31;59(71):10656-10659. doi: 10.1039/d3cc03221c. PMID:37581220<ref>PMID:37581220</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 8q1n" style="background-color:#fffaf0;"></div>
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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: Chang JY]]
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[[Category: Gasper R]]
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[[Category: Schmeing S]]
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[[Category: T Hart P]]

Revision as of 06:27, 6 September 2023

Cyclic peptide binder of the WBM-site of WDR5

PDB ID 8q1n

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