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2l8e

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==Solution NMR structure of FCS domain of Human Polyhomeotic Homolog 1 (HPH1)==
==Solution NMR structure of FCS domain of Human Polyhomeotic Homolog 1 (HPH1)==
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<StructureSection load='2l8e' size='340' side='right'caption='[[2l8e]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
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<StructureSection load='2l8e' size='340' side='right'caption='[[2l8e]]' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[2l8e]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L8E OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L8E FirstGlance]. <br>
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<table><tr><td colspan='2'>[[2l8e]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L8E OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L8E FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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">Solution NMR</td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PHC1, EDR1, PH1 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=ZN:ZINC+ION'>ZN</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=2l8e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l8e OCA], [https://pdbe.org/2l8e PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l8e RCSB], [https://www.ebi.ac.uk/pdbsum/2l8e PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l8e ProSAT]</span></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=2l8e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l8e OCA], [https://pdbe.org/2l8e PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l8e RCSB], [https://www.ebi.ac.uk/pdbsum/2l8e PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l8e ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
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[[https://www.uniprot.org/uniprot/PHC1_HUMAN PHC1_HUMAN]] Autosomal recessive primary microcephaly. The disease is caused by mutations affecting the gene represented in this entry.
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[https://www.uniprot.org/uniprot/PHC1_HUMAN PHC1_HUMAN] Autosomal recessive primary microcephaly. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
== Function ==
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[[https://www.uniprot.org/uniprot/PHC1_HUMAN PHC1_HUMAN]] Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. Required for proper control of cellular levels of GMNN expression.<ref>PMID:23418308</ref>
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[https://www.uniprot.org/uniprot/PHC1_HUMAN PHC1_HUMAN] Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. Required for proper control of cellular levels of GMNN expression.<ref>PMID:23418308</ref>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Human]]
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Ilangovan, U]]
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[[Category: Ilangovan U]]
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[[Category: Kim, C]]
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[[Category: Kim C]]
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[[Category: Dna binding protein]]
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Current revision

Solution NMR structure of FCS domain of Human Polyhomeotic Homolog 1 (HPH1)

PDB ID 2l8e

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