6ujq: Difference between revisions

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OCA

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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=6ujq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ujq OCA], [https://pdbe.org/6ujq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6ujq RCSB], [https://www.ebi.ac.uk/pdbsum/6ujq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6ujq ProSAT]</span></td></tr>
 </table>
-== Disease ==
-[https://www.uniprot.org/uniprot/HHAT_HUMAN HHAT_HUMAN] Chondrodysplasia-disorder of sex development syndrome. The disease is caused by variants affecting the gene represented in this entry.
 == Function ==
-[https://www.uniprot.org/uniprot/HHAT_HUMAN HHAT_HUMAN] Palmitoyl acyltransferase that catalyzes N-terminal palmitoylation of SHH; which is required for SHH signaling (PubMed:18534984, PubMed:31875564, PubMed:24784881). It also catalyzes N-terminal palmitoylation of DHH (PubMed:24784881). Promotes the transfer of palmitoyl-CoA from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane, where SHH palmitoylation occurs (PubMed:31875564). It is an essential factor for proper embryonic development and testicular organogenesis (PubMed:24784881).<ref>PMID:11486055</ref> <ref>PMID:18534984</ref> <ref>PMID:24784881</ref> <ref>PMID:31875564</ref>
+[https://www.uniprot.org/uniprot/U5YJP1_HUMAN U5YJP1_HUMAN]
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 == Publication Abstract from PubMed ==