6oip: Difference between revisions

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'''Unreleased structure'''


The entry 6oip is ON HOLD  until Paper Publication
==Crystal structure of MYST acetyltransferase domain in complex with inhibitor 34==
<StructureSection load='6oip' size='340' side='right'caption='[[6oip]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6oip]] is a 1 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=6OIP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6OIP 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]] 1.8&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ALY:N(6)-ACETYLLYSINE'>ALY</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MLS:2-fluoro-3-methyl-N-[(naphthalen-2-yl)sulfonyl]benzohydrazide'>MLS</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=6oip FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6oip OCA], [https://pdbe.org/6oip PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6oip RCSB], [https://www.ebi.ac.uk/pdbsum/6oip PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6oip ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/KAT8_HUMAN KAT8_HUMAN] Histone acetyltransferase which may be involved in transcriptional activation. May influence the function of ATM. As part of the MSL complex it is involved in acetylation of nucleosomal histone H4 producing specifically H4K16ac. As part of the NSL complex it may be involved in acetylation of nucleosomal histone H4 on several lysine residues. That activity is less specific than the one of the MSL complex.<ref>PMID:12397079</ref> <ref>PMID:15923642</ref> <ref>PMID:20018852</ref>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
A high-throughput screen for inhibitors of the histone acetyltransferase, KAT6A, led to identification of an aryl sulfonohydrazide derivative that inhibited KAT6A with an IC50 of 0.87M. Elaboration of the structure-activity relationship (SAR) and medicinal chemistry optimization led to discovery of WM-8014 (84), a highly potent inhibitor of KAT6A (IC50 = 0.008 M). WM-8014 competes with Ac-CoA and X-ray crystallographic analysis demonstrated binding to the Ac-CoA binding site. Through inhibition of KAT6A activity, WM-8014 induces cellular senescence and represents a unique pharmacological tool.


Authors: Hermans, S.J., Chung, M.C., Parker, M.W., Thomas, T., Baell, J.B.
Discovery of benzoylsulfonohydrazides as potent inhibitors of the histone acetyltransferase KAT6A.,Leaver D, Cleary B, Nguyen NT, Priebbenow DL, Lagiakos HR, Sanchez J, Xue L, Huang F, Sun Y, Mujumdar P, Mudududdla R, Varghese S, Teguh S, Charman SA, White K, Katneni K, Cuellar M, Strasser J, Dahlin J, Walters MA, Street I, Monahan B, Jarman KE, Jousset Sabroux H, Falk H, Chung M, Hermans S, Parker MW, Thomas T, Baell JB J Med Chem. 2019 Jun 29. doi: 10.1021/acs.jmedchem.9b00665. PMID:31256587<ref>PMID:31256587</ref>


Description: Crystal structure of MYST acetyltransferase domain in complex with inhibitor
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Thomas, T]]
<div class="pdbe-citations 6oip" style="background-color:#fffaf0;"></div>
[[Category: Parker, M.W]]
 
[[Category: Baell, J.B]]
==See Also==
[[Category: Chung, M.C]]
*[[Histone acetyltransferase 3D structures|Histone acetyltransferase 3D structures]]
[[Category: Hermans, S.J]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Baell JB]]
[[Category: Chung MC]]
[[Category: Hermans SJ]]
[[Category: Parker MW]]
[[Category: Thomas T]]

Latest revision as of 07:11, 11 October 2023

Crystal structure of MYST acetyltransferase domain in complex with inhibitor 34

6oip, resolution 1.80Å

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