7xw9

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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=7xw9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xw9 OCA], [https://pdbe.org/7xw9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xw9 RCSB], [https://www.ebi.ac.uk/pdbsum/7xw9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xw9 ProSAT]</span></td></tr>
 </table>
-== Disease ==
-[https://www.uniprot.org/uniprot/TRFR_HUMAN TRFR_HUMAN] Resistance to thyrotropin-releasing hormone syndrome. The disease is caused by variants affecting the gene represented in this entry.
+==See Also==
-== Function ==
+*[[Transducin 3D structures|Transducin 3D structures]]
-[https://www.uniprot.org/uniprot/TRFR_HUMAN TRFR_HUMAN] Receptor for thyrotropin-releasing hormone (TRH). Upon ligand binding, this G-protein-coupled receptor triggers activation of the phosphatidylinositol (IP3)-calcium-protein kinase C (PKC) pathway.<ref>PMID:26735259</ref> <ref>PMID:9141550</ref>
-== References ==
-<references/>
 __TOC__
 </StructureSection>