4nn2
From Proteopedia
(Difference between revisions)
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==Protein Crystal Structure of Human Borjeson-Forssman-Lehmann Syndrome Associated Protein PHF6== | ==Protein Crystal Structure of Human Borjeson-Forssman-Lehmann Syndrome Associated Protein PHF6== | ||
| - | <StructureSection load='4nn2' size='340' side='right' caption='[[4nn2]], [[Resolution|resolution]] 1.47Å' scene=''> | + | <StructureSection load='4nn2' size='340' side='right'caption='[[4nn2]], [[Resolution|resolution]] 1.47Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4nn2]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4nn2]] 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=4NN2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4NN2 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <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=4nn2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4nn2 OCA], [https://pdbe.org/4nn2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4nn2 RCSB], [https://www.ebi.ac.uk/pdbsum/4nn2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4nn2 ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/PHF6_HUMAN PHF6_HUMAN] Borjeson-Forssman-Lehmann syndrome. The disease is caused by mutations affecting the gene represented in this entry. |
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/PHF6_HUMAN PHF6_HUMAN] Transcriptional regulator that associates with ribosomal RNA promoters and suppresses ribosomal RNA (rRNA) transcription.<ref>PMID:23229552</ref> |
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: Li | + | [[Category: Large Structures]] |
| - | [[Category: Liu | + | [[Category: Li F]] |
| - | [[Category: Mei | + | [[Category: Liu Z]] |
| - | [[Category: Shi | + | [[Category: Mei Y]] |
| - | [[Category: Wu | + | [[Category: Shi Y]] |
| - | [[Category: Zhang | + | [[Category: Wu J]] |
| - | + | [[Category: Zhang J]] | |
| - | + | ||
Revision as of 08:35, 11 January 2023
Protein Crystal Structure of Human Borjeson-Forssman-Lehmann Syndrome Associated Protein PHF6
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Categories: Homo sapiens | Large Structures | Li F | Liu Z | Mei Y | Shi Y | Wu J | Zhang J
