9fq1
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of the disease-causing mutant P20S of human KCTD1== | |
| - | + | <StructureSection load='9fq1' size='340' side='right'caption='[[9fq1]], [[Resolution|resolution]] 2.60Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[9fq1]] is a 5 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=9FQ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9FQ1 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.6Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr> |
| - | [[Category: Balasco | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9fq1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9fq1 OCA], [https://pdbe.org/9fq1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9fq1 RCSB], [https://www.ebi.ac.uk/pdbsum/9fq1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9fq1 ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: Esposito | + | == Disease == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/KCTD1_HUMAN KCTD1_HUMAN] Scalp-ear-nipple syndrome. The disease is caused by mutations affecting the gene represented in this entry. |
| - | [[Category: | + | == Function == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/KCTD1_HUMAN KCTD1_HUMAN] May repress the transcriptional activity of AP-2 family members, including TFAP2A, TFAP2B and TFAP2C to various extent.<ref>PMID:18358072</ref> <ref>PMID:19115315</ref> |
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Balasco N]] | ||
| + | [[Category: Berisio R]] | ||
| + | [[Category: Esposito L]] | ||
| + | [[Category: Ruggiero A]] | ||
| + | [[Category: Smaldone G]] | ||
| + | [[Category: Vitagliano L]] | ||
Current revision
Structure of the disease-causing mutant P20S of human KCTD1
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