8jl4: Difference between revisions

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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=8jl4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8jl4 OCA], [https://pdbe.org/8jl4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8jl4 RCSB], [https://www.ebi.ac.uk/pdbsum/8jl4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8jl4 ProSAT]</span></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=8jl4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8jl4 OCA], [https://pdbe.org/8jl4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8jl4 RCSB], [https://www.ebi.ac.uk/pdbsum/8jl4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8jl4 ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/HGNAT_HUMAN HGNAT_HUMAN] Sanfilippo syndrome type C;Retinitis pigmentosa. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/HGNAT_HUMAN HGNAT_HUMAN] Lysosomal acetyltransferase that acetylates the non-reducing terminal alpha-glucosamine residue of intralysosomal heparin or heparan sulfate, converting it into a substrate for luminal alpha-N-acetyl glucosaminidase.<ref>PMID:16960811</ref> <ref>PMID:17033958</ref> <ref>PMID:19823584</ref> <ref>PMID:20650889</ref>
== References ==
<references/>
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</StructureSection>
</StructureSection>
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