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CHEBI:144321 - N4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-Asn residue

ChEBI IDCHEBI:144321
ChEBI NameN4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-Asn residue
Stars
ASCII NameN(4)-{alpha-D-Manp-(1->3)-[alpha-D-Manp-(1->6)]-beta-D-Manp-(1->4)-beta-D-GlcpNAc-(1->4)-D-GlcpNAc-yl}-L-Asn residue
DefinitionAn N4-glycosylated L-asparagine residue resulting from the formal condensation of the side-chain carboxamide group of the L-asparagine residue at positions 417, 423, and 556 of the genome polyprotein of hepatitis C virus subtype 1a (positions 35, 41, and 174, respectivey, in PMID:18187336) with the hemiacetal group of α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc.
Last Modified4 March 2025
SubmitterGareth Owen
DownloadsMolfile
FormulaC38H62N4O27
Net Charge0
Average Mass1006.915
Monoisotopic Mass1006.36014
SMILES*N[C@@H](CC(=O)NC1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@H](CO[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)[C@@H](O)[C@H](O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)[C@@H]3O)[C@H](O)[C@H]2NC(C)=O)[C@H](O)[C@H]1NC(C)=O)C(*)=O
ChEBI Ontology
Outgoing Relation(s)
N4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-Asn residue (CHEBI:144321) has functional parent L-asparagine residue (CHEBI:50347)
N4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-Asn residue (CHEBI:144321) has functional parent α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc (CHEBI:53458)
N4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-Asn residue (CHEBI:144321) is a N4-glycosylated L-asparagine residue (CHEBI:59108)
Synonym  Source
N4-{α-D-Manp-(1→3)-[α-D-Manp-(1→6)]-β-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc-yl}-L-asparagine residueChEBI
UniProt Name  Source
an N4-{α-D-Man-(1→3)-[α-D-Man-(1→6)]-β-D-Man-(1→4)-β-D-GlcNAc-(1→4)-β-D-GlcNAc}-L-Asn residueUniProt
Citations