6uhy

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==WDR5 in complex with Myc site fragment inhibitor==
==WDR5 in complex with Myc site fragment inhibitor==
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<StructureSection load='6uhy' size='340' side='right'caption='[[6uhy]]' scene=''>
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<StructureSection load='6uhy' size='340' side='right'caption='[[6uhy]], [[Resolution|resolution]] 1.26&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6UHY OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6UHY FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6uhy]] 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=6UHY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6UHY FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6uhy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6uhy OCA], [http://pdbe.org/6uhy PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6uhy RCSB], [http://www.ebi.ac.uk/pdbsum/6uhy PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6uhy ProSAT]</span></td></tr>
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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]] 1.26&#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=Q8G:1-cyclohexyl-1H-benzimidazole-5-carboxylic+acid'>Q8G</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=6uhy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6uhy OCA], [https://pdbe.org/6uhy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6uhy RCSB], [https://www.ebi.ac.uk/pdbsum/6uhy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6uhy ProSAT]</span></td></tr>
</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/WDR5_HUMAN WDR5_HUMAN] Contributes to histone modification. May position the N-terminus of histone H3 for efficient trimethylation at 'Lys-4'. As part of the MLL1/MLL complex it is involved in methylation and dimethylation at 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. As part of the NSL complex it may be involved in acetylation of nucleosomal histone H4 on several lysine residues. May regulate osteoblasts differentiation.<ref>PMID:19556245</ref> <ref>PMID:19103755</ref> <ref>PMID:20018852</ref> <ref>PMID:16600877</ref> <ref>PMID:16829960</ref>
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==See Also==
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*[[WD-repeat protein 3D structures|WD-repeat protein 3D structures]]
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Fesik SW]]
[[Category: Fesik SW]]
[[Category: Wang F]]
[[Category: Wang F]]

Current revision

WDR5 in complex with Myc site fragment inhibitor

PDB ID 6uhy

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