• Compound ID: 19942
  

  a-D-Manp-(1-2)-a-D-Manp-(1-3)-+ | a-D-Manp-(1-2)-+ | | | a-D-Manp-(1--P--6)--a-D-Manp-(1-6)-a-D-Manp-(1-6)-+ | a-D-Manp-(1-6)-+ | | | a-D-Manp-(1-2)-a-D-Manp-(1-6)-+ | | | a-D-Man-(1-2)-+ | | | | | a-D-Manp-(1--P--6)--a-D-Manp-(1-2)-a-D-Manp-(1-3)-b-Manp-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/

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  Structure type: structural motif or average structure
  Aglycon: (->4) Asn-X-Ser/Thr (protein)
  Compound class: N-glycan
  Reference(s) to other database(s): GTC:G20960GK
  
   
  
  Carbohydrate Research 2013, "Characterization of the Ashbya gossypii secreted N-glycome and genomic insights into its N-glycosylation pathway"
  CSDB ID 44833 (all data & tools)
• Compound ID: 21965
  

  D-Rib-ol-(1-5)-Subst Subst = lumichrome = SMILES CC1=CC(N=C2C({2}N3)=O)=C(C=C1C){5}NC2=NC3=O

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  Structure type: monomer
  Trivial name: riboflavin, vitamin B2
  Compound class: glycoside
  
   
  
  New Biotechnology 2019, "Physiological characterization of a pyrimidine auxotroph exposes link between uracil phosphoribosyltransferase regulation and riboflavin production in Ashbya gossypii"
  CSDB ID 49669 (all data & tools)

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