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1.
(
Organism ID:
9778)
Aspergillus
flavus
(
NCBI TaxID 5059
,
species name lookup
)
Taxonomic group:
fungi
Phylum:
Ascomycota
The following compound(s) are assigned to this organism:
Compound ID:
1030
-6)-b-D-GlcpNAc-(1-
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Structure type:
homopolymer
Trivial name:
poly-β-1,6-GlcNAc (PGA), biofilm, poly-b-(1-6)-N-acetyl-D-glucosamine (PNAG), poly-β-N-acetyl-glucosamine (PNAG), PNAG, poly-N-acetylglucosamine, PNAG
Compound class:
CPS, EPS, O-polysaccharide, glucan, polysaccharide
Reference(s) to other database(s):
GTC:G36952FI, GlycomeDB:
11210
Engineering (Beijing)
2024, "Antibodies targeting a conserved surface polysaccharide are protective against a wide range of microbial pathogens producing β-1–6-linked poly-N-acetylglucosamine (PNAG)"
CSDB ID 15645
(all data & tools)
Compound ID:
18709
R-2HOSte-(1-2)-+ | b-D-Glcp-(1-1)-Subst Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO
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Structure type:
monomer ; 778.5823 [M+Na]+
C43H81NO9
Trivial name:
flavuside A
Compound class:
glycosphingolipid, cerebroside
Chemical and Pharmaceutical Bulletin
2011, "Flavusides A and B, antibacterial cerebrosides from the marine-derived fungus Aspergillus flavus"
CSDB ID 43679
(all data & tools)
Compound ID:
18710
b-D-Glcp-(1-1)-+ | R-2HOC18={t3}-(1-2)-Subst Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO
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Structure type:
monomer ; 776.5644 [M+Na]+
C43H79NO9
Trivial name:
flavuside B
Compound class:
glycosphingolipid, cerebroside
Chemical and Pharmaceutical Bulletin
2011, "Flavusides A and B, antibacterial cerebrosides from the marine-derived fungus Aspergillus flavus"
CSDB ID 43680
(all data & tools)
Compound ID:
22618
Pam-(1-2)-+ | ?%Subst-(1-4)-+ | /Variants 0/-+ | | | ?%Subst-(1-3)-b-D-GlcpN(%)Me-(1-4)-{{{-b-D-GlcpNAc-(1-4)-}}}/n=1-3/-b-D-GlcpN | ?%Subst-(1-6)-+ /Variants 0/ is: ?%S-6)- OR (exclusively) ?%S-?)-?%D-Fucp?(%)Me-(1-6)- Subst = Ac or O-linked Cm
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Structure type:
oligomer
Compound class:
lipochitooligosaccharide
Nature Communications
2020, "Lipo-chitooligosaccharides as regulatory signals of fungal growth and development"
CSDB ID 50880
(all data & tools)
Compound ID:
20119
b-D-Glcp-(1-1)-+ | R-2HOC18={t3}-(1-2)-Subst Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO
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Structure type:
monomer
Trivial name:
flavuside A, flavuside B
Compound class:
glycosphingolipid, glycoside, cerebroside
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51460
(all data & tools)
Compound ID:
23049
R-2HOSte-(1-2)-+ | b-D-Glcp-(1-1)-Subst Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO
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Structure type:
monomer
Trivial name:
flavuside B
Compound class:
glycoside
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51461
(all data & tools)
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