8jl4
From Proteopedia
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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/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
membrane proteins
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Categories: Homo sapiens | Large Structures | Ge JP | Xu RS | Yu J
