6s4l

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m (Protected "6s4l" [edit=sysop:move=sysop])
Current revision (12:35, 24 January 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6s4l is ON HOLD
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==Structure of human KCTD1==
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<StructureSection load='6s4l' size='340' side='right'caption='[[6s4l]], [[Resolution|resolution]] 2.42&Aring;' scene=''>
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Authors: Pinkas, D.M., Bufton, J.C., Fox, A.E., Pike, A.C.W., Newman, J.A., Krojer, T., Shrestha, L., Burgess-Brown, N.A., von Delft, F., Arrowsmith, C., Edwards, A., Bountra, C., Bullock, A.N.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6s4l]] 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=6S4L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6S4L FirstGlance]. <br>
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Description: Structure of human KCTD1
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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]] 2.42&#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=IOD:IODIDE+ION'>IOD</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
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[[Category: Pinkas, D.M]]
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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=6s4l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6s4l OCA], [https://pdbe.org/6s4l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6s4l RCSB], [https://www.ebi.ac.uk/pdbsum/6s4l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6s4l ProSAT]</span></td></tr>
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[[Category: Pike, A.C.W]]
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</table>
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[[Category: Fox, A.E]]
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== Disease ==
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[[Category: Shrestha, L]]
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[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.
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[[Category: Newman, J.A]]
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== Function ==
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[[Category: Edwards, A]]
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[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>
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[[Category: Burgess-Brown, N.A]]
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== References ==
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[[Category: Krojer, T]]
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<references/>
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[[Category: Von Delft, F]]
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__TOC__
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[[Category: Bountra, C]]
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</StructureSection>
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[[Category: Bullock, A.N]]
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[[Category: Homo sapiens]]
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[[Category: Arrowsmith, C]]
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[[Category: Large Structures]]
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[[Category: Bufton, J.C]]
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[[Category: Arrowsmith C]]
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[[Category: Bountra C]]
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[[Category: Bufton JC]]
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[[Category: Bullock AN]]
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[[Category: Burgess-Brown NA]]
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[[Category: Edwards A]]
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[[Category: Fox AE]]
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[[Category: Krojer T]]
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[[Category: Newman JA]]
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[[Category: Pike ACW]]
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[[Category: Pinkas DM]]
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[[Category: Shrestha L]]
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[[Category: Von Delft F]]

Current revision

Structure of human KCTD1

PDB ID 6s4l

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Proteopedia Page Contributors and Editors (what is this?)

OCA

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