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New page: left|200px<br /> <applet load="1m1e" size="450" color="white" frame="true" align="right" spinBox="true" caption="1m1e, resolution 2.10Å" /> '''Beta-catenin armadi...
 
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[[Image:1m1e.gif|left|200px]]<br />
<applet load="1m1e" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1m1e, resolution 2.10&Aring;" />
'''Beta-catenin armadillo repeat domain bound to ICAT'''<br />


==Overview==
==Beta-catenin armadillo repeat domain bound to ICAT==
In the canonical Wnt signaling pathway, beta-catenin activates target, genes through its interactions with Tcf/Lef-family transcription factors, and additional transcriptional coactivators. The crystal structure of, ICAT, an inhibitor of beta-catenin-mediated transcription, bound to the, armadillo repeat domain of beta-catenin, has been determined. ICAT, contains an N-terminal helilical domain that binds to repeats 11 and 12 of, beta-catenin, and an extended C-terminal region that binds to repeats 5-10, in a manner similar to that of Tcfs and other beta-catenin ligands., Full-length ICAT dissociates complexes of beta-catenin, Lef-1, and the, transcriptional coactivator p300, whereas the helical domain alone, selectively blocks binding to p300. The C-terminal armadillo repeats of, beta-catenin may be an attractive target for compounds designed to disrupt, aberrant beta-catenin-mediated transcription associated with various, cancers.
<StructureSection load='1m1e' size='340' side='right'caption='[[1m1e]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1m1e]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1M1E OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1M1E 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]] 2.1&#8491;</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=1m1e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1m1e OCA], [https://pdbe.org/1m1e PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1m1e RCSB], [https://www.ebi.ac.uk/pdbsum/1m1e PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1m1e ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/CNBP1_HUMAN CNBP1_HUMAN] Prevents the interaction between CTNNB1 and TCF family members, and acts as negative regulator of the Wnt signaling pathway.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/m1/1m1e_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1m1e ConSurf].
<div style="clear:both"></div>


==About this Structure==
==See Also==
1M1E is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1M1E OCA].
*[[Catenin 3D structures|Catenin 3D structures]]
 
__TOC__
==Reference==
</StructureSection>
ICAT inhibits beta-catenin binding to Tcf/Lef-family transcription factors and the general coactivator p300 using independent structural modules., Daniels DL, Weis WI, Mol Cell. 2002 Sep;10(3):573-84. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12408825 12408825]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Daniels DL]]
[[Category: Daniels, D.L.]]
[[Category: Weis WI]]
[[Category: Weis, W.I.]]
[[Category: armadillo repeats]]
[[Category: cell adhesion]]
[[Category: cytoskeleton]]
[[Category: transciption factor]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:06:18 2007''

Latest revision as of 07:38, 14 February 2024

Beta-catenin armadillo repeat domain bound to ICAT

1m1e, resolution 2.10Å

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