6ht0
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of MLLT1 (ENL) YEATS domain in complexed with compound 94== | |
| + | <StructureSection load='6ht0' size='340' side='right' caption='[[6ht0]], [[Resolution|resolution]] 1.80Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[6ht0]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6HT0 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6HT0 FirstGlance]. <br> | ||
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=GQ8:1-cyclopropyl-~{N}-[2-[[(2~{S})-2-methylpyrrolidin-1-yl]methyl]-3~{H}-benzimidazol-5-yl]indazole-5-carboxamide'>GQ8</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | ||
| + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6ht1|6ht1]]</td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6ht0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ht0 OCA], [http://pdbe.org/6ht0 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ht0 RCSB], [http://www.ebi.ac.uk/pdbsum/6ht0 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ht0 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/ENL_HUMAN ENL_HUMAN]] A chromosomal aberration involving MLLT1 is associated with acute leukemias. Translocation t(11;19)(q23;p13.3) with KMT2A/MLL1. The result is a rogue activator protein. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/ENL_HUMAN ENL_HUMAN]] Component of the super elongation complex (SEC), a complex required to increase the catalytic rate of RNA polymerase II transcription by suppressing transient pausing by the polymerase at multiple sites along the DNA.<ref>PMID:20159561</ref> <ref>PMID:20471948</ref> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | YEATS domain (YD) containing proteins are an emerging class of epigenetic targets in drug discovery. Dysregulation of these modified lysine binding proteins has been linked to the onset and progression of cancers. We herein report the discovery and characterisation of the first small molecule chemical probe, SGC-iMLLT, for the YD of MLLT1 (ENL/YEATS1) and MLLT3 (AF9/YEATS3). SGC-iMLLT is a potent and selective inhibitor of MLLT1/3 - histone interactions. Excellent selectivity over other human YD proteins (YEATS2/4) and bromodomains was observed. Furthermore, our probe displays cellular target engagement of MLLT1 and MLLT3. The first small molecule X-ray co-crystal structures with the MLLT1 YD are also reported. This first in class probe molecule can be used to understand MLLT1/3 associated biology and the therapeutic potential of small molecule YD inhibitors. | ||
| - | + | Discovery of an MLLT1/3 YEATS Domain Chemical Probe.,Moustakim M, Christott T, Monteiro OP, Bennett J, Giroud C, Ward J, Rogers CM, Smith P, Panagakou I, Saez LD, Felce SL, Gamble V, Gileadi C, Halidi N, Heidenreich D, Chaikuad A, Knapp S, Huber KVM, Farnie G, Heer J, Manevski N, Poda G, Al-Awar R, Dixon DJ, Fedorov O, Brennan P Angew Chem Int Ed Engl. 2018 Oct 5. doi: 10.1002/anie.201810617. PMID:30288907<ref>PMID:30288907</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| + | <div class="pdbe-citations 6ht0" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Arrowsmith, C H]] | ||
| + | [[Category: Bountra, C]] | ||
| + | [[Category: Brennan, P E]] | ||
[[Category: Chaikuad, A]] | [[Category: Chaikuad, A]] | ||
| + | [[Category: Edwards, A M]] | ||
| + | [[Category: Fedorov, O]] | ||
[[Category: Heidenreich, D]] | [[Category: Heidenreich, D]] | ||
[[Category: Knapp, S]] | [[Category: Knapp, S]] | ||
| - | [[Category: Edwards, A.M]] | ||
| - | [[Category: Arrowsmith, C.H]] | ||
| - | [[Category: Brennan, P.E]] | ||
| - | [[Category: Fedorov, O]] | ||
| - | [[Category: Structural Genomics Consortium (Sgc)]] | ||
| - | [[Category: Bountra, C]] | ||
[[Category: Moustakim, M]] | [[Category: Moustakim, M]] | ||
| + | [[Category: Structural genomic]] | ||
| + | [[Category: Chemical probe]] | ||
| + | [[Category: Enl]] | ||
| + | [[Category: Inhibitor]] | ||
| + | [[Category: Mllt1]] | ||
| + | [[Category: Sgc]] | ||
| + | [[Category: Transcription]] | ||
| + | [[Category: Yeats domain]] | ||
Revision as of 08:12, 17 October 2018
Crystal structure of MLLT1 (ENL) YEATS domain in complexed with compound 94
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Categories: Arrowsmith, C H | Bountra, C | Brennan, P E | Chaikuad, A | Edwards, A M | Fedorov, O | Heidenreich, D | Knapp, S | Moustakim, M | Structural genomic | Chemical probe | Enl | Inhibitor | Mllt1 | Sgc | Transcription | Yeats domain
