6zc4: Difference between revisions

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== Structural highlights ==

<table><tr><td colspan='2'>[[6zc4]] is a 2 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=6ZC4 OCA]. For a guided tour on the structure components use [https://proteopedia.org/fgij/fg.htm?mol=6ZC4 FirstGlance].

</td></tr><tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=QEZ:5-bromanyl-2-(5,6,7,8-tetrahydronaphthalen-2-ylsulfonylamino)benzoic+acid'>QEZ</scene></td></tr>

</td></tr><tr id='method'><td class="sblockLbl">[[Empirical_models|Method:]]</td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.85Å</td></tr>

<tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=QEZ:5-bromanyl-2-(5,6,7,8-tetrahydronaphthalen-2-ylsulfonylamino)benzoic+acid'>QEZ</scene></td></tr>

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[https://proteopedia.org/fgij/fg.htm?mol=6zc4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zc4 OCA], [https://pdbe.org/6zc4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zc4 RCSB], [https://www.ebi.ac.uk/pdbsum/6zc4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zc4 ProSAT]</td></tr>

</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.

[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]

[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN] Involved in the signal transduction pathway mediated by multiple Wnt genes.[UniProtKB:Q61062]

__TOC__

</StructureSection>

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@@ Line 4: / Line 4: @@
 == Structural highlights ==
 <table><tr><td colspan='2'>[[6zc4]] is a 2 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=6ZC4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ZC4 FirstGlance]. <br>
-</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=QEZ:5-bromanyl-2-(5,6,7,8-tetrahydronaphthalen-2-ylsulfonylamino)benzoic+acid'>QEZ</scene></td></tr>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.85&#8491;</td></tr>
+<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=QEZ:5-bromanyl-2-(5,6,7,8-tetrahydronaphthalen-2-ylsulfonylamino)benzoic+acid'>QEZ</scene></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=6zc4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zc4 OCA], [https://pdbe.org/6zc4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zc4 RCSB], [https://www.ebi.ac.uk/pdbsum/6zc4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zc4 ProSAT]</span></td></tr>
 </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.
+[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]
+[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN] Involved in the signal transduction pathway mediated by multiple Wnt genes.[UniProtKB:Q61062]
 __TOC__
 </StructureSection>