9foe

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'''Unreleased structure'''
 
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The entry 9foe is ON HOLD
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==Crystal structure of the PWWP1 domain of NSD2 bound by compound 7.==
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<StructureSection load='9foe' size='340' side='right'caption='[[9foe]], [[Resolution|resolution]] 1.96&Aring;' scene=''>
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Authors: Collie, G.W.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9foe]] 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=9FOE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9FOE FirstGlance]. <br>
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Description: Crystal structure of the PWWP1 domain of NSD2 bound by compound 7.
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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]] 1.963&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1IEF:1-[[(2~{S})-1-[4-[ethyl(pyridin-4-ylmethyl)amino]-6-methyl-pyrimidin-2-yl]pyrrolidin-2-yl]methyl]urea'>A1IEF</scene></td></tr>
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[[Category: Collie, G.W]]
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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=9foe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9foe OCA], [https://pdbe.org/9foe PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9foe RCSB], [https://www.ebi.ac.uk/pdbsum/9foe PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9foe ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/NSD2_HUMAN NSD2_HUMAN] Wolf-Hirschhorn syndrome. A chromosomal aberration involving WHSC1 is a cause of multiple myeloma tumors. Translocation t(4;14)(p16.3;q32.3) with IgH. WHSC1 is located in the Wolf-Hirschhorn syndrome (WHS) critical region. WHS results from by sub-telomeric deletions in the short arm of chromosome 4. WHSC1 is deleted in every case, however deletion of linked genes contributes to both the severity of the core characteristics and the presence of the additional syndromic problems.
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== Function ==
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[https://www.uniprot.org/uniprot/NSD2_HUMAN NSD2_HUMAN] Histone methyltransferase with histone H3 'Lys-27' (H3K27me) methyltransferase activity. Isoform 2 may act as a transcription regulator that binds DNA and suppresses IL5 transcription through HDAC recruitment.<ref>PMID:11152655</ref> <ref>PMID:16115125</ref> <ref>PMID:18172012</ref>
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== References ==
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<references/>
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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: Collie GW]]

Current revision

Crystal structure of the PWWP1 domain of NSD2 bound by compound 7.

PDB ID 9foe

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