7z8p

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(New page: '''Unreleased structure''' The entry 7z8p is ON HOLD Authors: Nai, F., Zalesak, F., Li, Y., Caflisch, A. Description: Crystal structure of YTHDF2 with compound ZA_166 [[Category: Unrel...)
Current revision (13:29, 1 February 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 7z8p is ON HOLD
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==Crystal structure of YTHDF2 with compound ZA_166==
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<StructureSection load='7z8p' size='340' side='right'caption='[[7z8p]], [[Resolution|resolution]] 1.97&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7z8p]] 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=7Z8P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7Z8P 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]] 1.97&#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=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=IFZ:3-bromanyl-~{N}-methyl-2~{H}-pyrazolo[4,3-d]pyrimidin-7-amine'>IFZ</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=7z8p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7z8p OCA], [https://pdbe.org/7z8p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7z8p RCSB], [https://www.ebi.ac.uk/pdbsum/7z8p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7z8p ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/YTHD2_HUMAN YTHD2_HUMAN] Specifically recognizes and binds N6-methyladenosine (m6A)-containing RNAs. M6A is a modification present at internal sites of mRNAs and some non-coding RNAs and plays a role in the efficiency of mRNA splicing, processing and stability. Acts as a regulator of mRNA stability: binding to m6A-containing mRNAs results in the localization of to mRNA decay sites, such as processing bodies (P-bodies), leading to mRNA degradation.<ref>PMID:22575960</ref> <ref>PMID:24284625</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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We report 17 small-molecule ligands that compete with N6-methyladenosine (m(6)A) for binding to the m(6)A-reader domain of YTHDF2 (YT521-B homology domain family 2). We determined their binding mode at high resolution by X-ray crystallography and quantified their affinity by a fluorescence-based binding assay. 6-Cyclopropyluracil and a pyrazolopyrimidine derivative have favorable ligand efficiencies of 0.47 and 0.38 kcal mol(-1) per non-hydrogen atom, respectively. They represent useful starting points for hit optimization.
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Authors: Nai, F., Zalesak, F., Li, Y., Caflisch, A.
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Fragment Ligands of the m(6)A-RNA Reader YTHDF2.,Nai F, Nachawati R, Zalesak F, Wang X, Li Y, Caflisch A ACS Med Chem Lett. 2022 Aug 17;13(9):1500-1509. doi:, 10.1021/acsmedchemlett.2c00303. eCollection 2022 Sep 8. PMID:36110386<ref>PMID:36110386</ref>
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Description: Crystal structure of YTHDF2 with compound ZA_166
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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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[[Category: Nai, F]]
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<div class="pdbe-citations 7z8p" style="background-color:#fffaf0;"></div>
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[[Category: Li, Y]]
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== References ==
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[[Category: Caflisch, A]]
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<references/>
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[[Category: Zalesak, F]]
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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: Caflisch A]]
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[[Category: Li Y]]
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[[Category: Nai F]]
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[[Category: Zalesak F]]

Current revision

Crystal structure of YTHDF2 with compound ZA_166

PDB ID 7z8p

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