5bxb: Difference between revisions

Line 1:

'''~~Unreleased structure~~'''

==Crystal structure of pentameric KCTD1 BTB domain form 1==

~~The entry~~ 5bxb is ~~ON HOLD until Paper Publication~~

== Structural highlights ==

<table><tr><td colspan='2'>[[5bxb]] is a 10 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5BXB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5BXB FirstGlance]. <br>

~~Authors~~: Ji, A.X., ~~Chu~~, A.~~, Prive, G~~.G.

</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5bxd|5bxd]], [[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=5bxb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5bxb OCA], [http://www.rcsb.org/pdb/explore.do?structureId=5bxb RCSB], [http://www.ebi.ac.uk/pdbsum/5bxb PDBsum]</span></td></tr>

~~Description:~~

</table>

[[~~Category~~: ~~Unreleased Structures~~]]

== Disease ==

[[~~Category~~: ~~Prive, G~~.G]]

[[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 ==

__TOC__

</StructureSection>

[[Category: Chu, A]]

[[Category: Ji, A.X]]

[[Category: Ji, A X]]

[[Category: Prive, G G]]

[[Category: Protein binding]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+==Crystal structure of pentameric KCTD1 BTB domain form 1==
+<StructureSection load='5bxb' size='340' side='right' caption='[[5bxb]], [[Resolution|resolution]] 2.17&Aring;' scene=''>
-The entry 5bxb is ON HOLD  until Paper Publication
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5bxb]] is a 10 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5BXB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5BXB FirstGlance]. <br>
-Authors: Ji, A.X., Chu, A., Prive, G.G.
+</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5bxd|5bxd]], [[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=5bxb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5bxb OCA], [http://www.rcsb.org/pdb/explore.do?structureId=5bxb RCSB], [http://www.ebi.ac.uk/pdbsum/5bxb PDBsum]</span></td></tr>
-Description:
+</table>
-[[Category: Unreleased Structures]]
+== Disease ==
-[[Category: Prive, G.G]]
+[[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: Ji, A.X]]
+[[Category: Ji, A X]]
+[[Category: Prive, G G]]
+[[Category: Protein binding]]