5bxd
From Proteopedia
(Difference between revisions)
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| - | ''' | + | ==Crystal structure of pentameric KCTD1 BTB domain form 2== |
| - | + | <StructureSection load='5bxd' size='340' side='right' caption='[[5bxd]], [[Resolution|resolution]] 1.80Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5bxd]] is a 5 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5BXD OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5BXD FirstGlance]. <br> | |
| - | + | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5bxb|5bxb]], [[5bxh|5bxh]]</td></tr> | |
| - | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5bxd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5bxd OCA], [http://www.rcsb.org/pdb/explore.do?structureId=5bxd RCSB], [http://www.ebi.ac.uk/pdbsum/5bxd PDBsum]</span></td></tr> | |
| - | + | </table> | |
| - | [[ | + | == Disease == |
| - | [[ | + | [[http://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. |
| + | == Function == | ||
| + | [[http://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: Chu, A]] | [[Category: Chu, A]] | ||
| - | [[Category: Ji, A | + | [[Category: Ji, A X]] |
| + | [[Category: Prive, G G]] | ||
| + | [[Category: Protein binding]] | ||
Revision as of 12:35, 2 September 2015
Crystal structure of pentameric KCTD1 BTB domain form 2
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