8cj2
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Urea-based foldamer inhibitor c3u_5 chimera in complex with ASF1 histone chaperone== | |
+ | <StructureSection load='8cj2' size='340' side='right'caption='[[8cj2]], [[Resolution|resolution]] 2.13Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[8cj2]] is a 8 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=8CJ2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CJ2 FirstGlance]. <br> | ||
+ | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.127Å</td></tr> | ||
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=66N:L-ALANINAMIDE'>66N</scene>, <scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=ALN:NAPHTHALEN-2-YL-3-ALANINE'>ALN</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=OUR:[AZANYL-[[(4~{S})-4-AZANYL-5-(CARBOXYAMINO)PENTYL]AMINO]METHYLIDENE]AZANIUM'>OUR</scene>, <scene name='pdbligand=QQ8:(4~{S})-4-azanyl-5-formamido-pentanamide'>QQ8</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=URL:[(2~{S})-2-azanyl-4-methyl-pentyl]carbamic+acid'>URL</scene></td></tr> | ||
+ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8cj2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cj2 OCA], [https://pdbe.org/8cj2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cj2 RCSB], [https://www.ebi.ac.uk/pdbsum/8cj2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cj2 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/ASF1A_HUMAN ASF1A_HUMAN] Histone chaperone that facilitates histone deposition and histone exchange and removal during nucleosome assembly and disassembly. Cooperates with chromatin assembly factor 1 (CAF-1) to promote replication-dependent chromatin assembly and with HIRA to promote replication-independent chromatin assembly. Required for the formation of senescence-associated heterochromatin foci (SAHF) and efficient senescence-associated cell cycle exit.<ref>PMID:10759893</ref> <ref>PMID:11897662</ref> <ref>PMID:12842904</ref> <ref>PMID:14718166</ref> <ref>PMID:15621527</ref> <ref>PMID:16151251</ref> <ref>PMID:15664198</ref> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | In the search for foldamer inhibitors of the histone chaperone ASF1, we explored the possibility of substituting four alpha-residues ( approximately one helix turn) by 3-urea segments and scanned the sequence of a short alpha-helical peptide known to bind ASF1. By analysing the impact of the different foldamer replacements within the peptide chain, we uncovered new binding modes of the peptide-urea chimeras to ASF1. | ||
- | + | Unexpected binding modes of inhibitors to the histone chaperone ASF1 revealed by a foldamer scanning approach.,Perrin ME, Li B, Mbianda J, Bakail M, Andre C, Moal G, Legrand P, Ropars V, Douat C, Ochsenbein F, Guichard G Chem Commun (Camb). 2023 Jun 22. doi: 10.1039/d3cc01891a. PMID:37347155<ref>PMID:37347155</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | [[Category: | + | </div> |
+ | <div class="pdbe-citations 8cj2" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Douat C]] | ||
+ | [[Category: Guichard G]] | ||
+ | [[Category: Legrand P]] | ||
+ | [[Category: Li B]] | ||
+ | [[Category: Mbianda J]] | ||
+ | [[Category: Ochsenbein F]] | ||
+ | [[Category: Perrin ME]] | ||
+ | [[Category: Ropars V]] |
Revision as of 05:40, 5 July 2023
Urea-based foldamer inhibitor c3u_5 chimera in complex with ASF1 histone chaperone
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Categories: Homo sapiens | Large Structures | Douat C | Guichard G | Legrand P | Li B | Mbianda J | Ochsenbein F | Perrin ME | Ropars V