6zc6: Difference between revisions

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==Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling==
==Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling==
<StructureSection load='6zc6' size='340' side='right'caption='[[6zc6]]' scene=''>
<StructureSection load='6zc6' size='340' side='right'caption='[[6zc6]], [[Resolution|resolution]] 1.58&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6ZC6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ZC6 FirstGlance]. <br>
<table><tr><td colspan='2'>[[6zc6]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6ZC6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ZC6 FirstGlance]. <br>
</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=6zc6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zc6 OCA], [https://pdbe.org/6zc6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zc6 RCSB], [https://www.ebi.ac.uk/pdbsum/6zc6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zc6 ProSAT]</span></td></tr>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=QEN:5-bromanyl-2-(naphthalen-2-ylsulfonylamino)benzoic+acid'>QEN</scene></td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">DVL3, KIAA0208 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=6zc6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zc6 OCA], [https://pdbe.org/6zc6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zc6 RCSB], [https://www.ebi.ac.uk/pdbsum/6zc6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zc6 ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
[[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN]] Autosomal dominant Robinow syndrome. The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN]] Involved in the signal transduction pathway mediated by multiple Wnt genes.[UniProtKB:Q61062]
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Human]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Heinemann U]]
[[Category: Heinemann, U]]
[[Category: Oschkinat H]]
[[Category: Oschkinat, H]]
[[Category: Roske Y]]
[[Category: Roske, Y]]
[[Category: Dvl]]
[[Category: Inhibitor]]
[[Category: Pdz]]
[[Category: Peptide binding protein]]
[[Category: Signalling]]
[[Category: Wnt]]