6t0x: Difference between revisions
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<StructureSection load='6t0x' size='340' side='right'caption='[[6t0x]], [[Resolution|resolution]] 1.36Å' scene=''> | <StructureSection load='6t0x' size='340' side='right'caption='[[6t0x]], [[Resolution|resolution]] 1.36Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6t0x]] is a 2 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6t0x]] 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=6T0X OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6T0X FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=M6W:(3~{S})-~{N}-methylpyrrolidine-3-carboxamide'>M6W</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.36Å</td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=M6W:(3~{S})-~{N}-methylpyrrolidine-3-carboxamide'>M6W</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=6t0x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6t0x OCA], [https://pdbe.org/6t0x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6t0x RCSB], [https://www.ebi.ac.uk/pdbsum/6t0x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6t0x ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/YTDC1_HUMAN YTDC1_HUMAN] RNA-binding protein that regulates alternative splice site selection.<ref>PMID:20167602</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Bedi | [[Category: Bedi RK]] | ||
[[Category: Caflisch | [[Category: Caflisch A]] | ||
[[Category: Huang | [[Category: Huang D]] | ||
[[Category: Sledz | [[Category: Sledz P]] | ||
Latest revision as of 15:51, 24 January 2024
Crystal structure of YTHDC1 with fragment 22 (ACA_DC1_001)Crystal structure of YTHDC1 with fragment 22 (ACA_DC1_001)
Structural highlights
FunctionYTDC1_HUMAN RNA-binding protein that regulates alternative splice site selection.[1] Publication Abstract from PubMedWe report a crystallographic analysis of small-molecule ligands of the human YTHDC1 domain that recognizes N6-methylated adenine (m(6)A) in RNA. The 30 binders are fragments (molecular weight < 300 g mol(-1)) that represent 10 different chemotypes identified by virtual screening. Despite the structural disorder of the binding site loop (residues 429-439), most of the 30 fragments emulate the two main interactions of the -NHCH3 group of m(6)A. These interactions are the hydrogen bond to the backbone carbonyl of Ser378 and the van der Waals contacts with the tryptophan cage. Different chemical groups are involved in the conserved binding motifs. Some of the fragments show favorable ligand efficiency for YTHDC1 and selectivity against other m(6)A reader domains. The structural information is useful for the design of modulators of m(6)A recognition by YTHDC1. Selectively Disrupting m(6)A-Dependent Protein-RNA Interactions with Fragments.,Bedi RK, Huang D, Wiedmer L, Li Y, Dolbois A, Wojdyla JA, Sharpe ME, Caflisch A, Sledz P ACS Chem Biol. 2020 Mar 2. doi: 10.1021/acschembio.9b00894. PMID:32101404[2] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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