6p7z

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(New page: '''Unreleased structure''' The entry 6p7z is ON HOLD Authors: Elkins, P.A., Bonnette, W.G. Description: Co-crystal Structure of human SMYD3 with Isoxazole Amides Inhibitors [[Category:...)
Current revision (14:54, 13 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6p7z is ON HOLD
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==Co-crystal Structure of human SMYD3 with Isoxazole Amides Inhibitors==
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<StructureSection load='6p7z' size='340' side='right'caption='[[6p7z]], [[Resolution|resolution]] 1.19&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6p7z]] 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=6P7Z OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6P7Z 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]] 1.19&#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=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=O41:5-cyclopropyl-N-[1-(methylsulfonyl)piperidin-4-yl]-1,2-oxazole-3-carboxamide'>O41</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=6p7z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6p7z OCA], [https://pdbe.org/6p7z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6p7z RCSB], [https://www.ebi.ac.uk/pdbsum/6p7z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6p7z ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/SMYD3_HUMAN SMYD3_HUMAN] Histone methyltransferase. Specifically methylates 'Lys-4' and 'Lys-5' of histone H3, inducing di- and tri-methylation, but not monomethylation. Plays an important role in transcriptional activation as a member of an RNA polymerase complex. Binds DNA containing 5'-CCCTCC-3' or 5'-GAGGGG-3' sequences.<ref>PMID:15235609</ref> <ref>PMID:22419068</ref>
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Authors: Elkins, P.A., Bonnette, W.G.
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==See Also==
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*[[Histone methyltransferase 3D structures|Histone methyltransferase 3D structures]]
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Description: Co-crystal Structure of human SMYD3 with Isoxazole Amides Inhibitors
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Elkins, P.A]]
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__TOC__
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[[Category: Bonnette, W.G]]
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Bonnette WG]]
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[[Category: Elkins PA]]

Current revision

Co-crystal Structure of human SMYD3 with Isoxazole Amides Inhibitors

PDB ID 6p7z

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