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1.
(
Organism ID:
8404)
Actinomadura
sp. ATCC 39727
(
Ancestor NCBI TaxID 93944
,
species name lookup
)
Later renamed to:
Nonomuraea gerenzanensis
ATCC 39727
Taxonomic group:
bacteria
Phylum:
Actinobacteria
The following compound(s) are assigned to this organism:
Compound ID:
14215
a-D-Manp-(1-1)-+ | Subst2-(1-2)-a-D-GlcpNA-(1-2)-Subst Subst = SMILES CN[C@H]6C(=O)N[C@@H]4Cc1ccc(cc1)Oc%11cc3cc(Oc2ccc(cc2Cl)C(O)C%10NC(=O)[C@H](NC(=O)[C@@H]3NC(=O)[C@@H](NC4=O)c5cc(cc(O)c5Cl)Oc7cc6ccc7O)c8cccc(c8)c9{1}c(O)cc(O)cc9[C@@H](C(=O)O)NC%10=O){2}c%11O; Subst2 = isolauric acid = SMILES CC(C)CCCCCCCC{1}C(=O)O
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Structure type:
oligomer
Trivial name:
A40926
Compound class:
glycoside
Microbiology
2015, "Engineered biosynthesis of enduracidin lipoglycopeptide antibiotics using the ramoplanin mannosyltransferase Ram29"
CSDB ID 47728
(all data & tools)
Compound ID:
14218
a-D-Manp-(1-1)-+ | Udo-(1-2)-a-D-GlcpNA-(1-2)-Subst Subst = SMILES CN[C@H]6C(=O)N[C@@H]4Cc1ccc(cc1)Oc%11cc3cc(Oc2ccc(cc2Cl)C(O)C%10NC(=O)[C@H](NC(=O)[C@@H]3NC(=O)[C@@H](NC4=O)c5cc(cc(O)c5Cl)Oc7cc6ccc7O)c8cccc(c8)c9{1}c(O)cc(O)cc9[C@@H](C(=O)O)NC%10=O){2}c%11O
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Structure type:
oligomer ; 1716
Trivial name:
A40926
Compound class:
glycoside
Antimicrobial Agents and Chemotherapy
1987, "A40926, a new glycopeptide antibiotic with anti-Neisseria activity"
CSDB ID 47731
(all data & tools)
Compound ID:
14219
a-D-Manp-(1-1)-+ | Udo-(1-2)-a-D-GlcpNA-(1-2)-Subst Subst = SMILES CN[C@H]6C(=O)N[C@@H]4Cc1ccc(cc1)Oc%11cc3cc(Oc2ccc(cc2Cl)C(O)C%10NC(=O)[C@H](NC(=O)[C@@H]3NC(=O)[C@@H](NC4=O)c5cc(cc(O)c5Cl)Oc7cc6ccc7O)c8cccc(c8)c9{1}c(O)cc(O)cc9[C@@H](C(=O)O)NC%10=O){2}c%11O
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Structure type:
oligomer ; 1758
Trivial name:
A40926
Compound class:
glycoside
Antimicrobial Agents and Chemotherapy
1987, "A40926, a new glycopeptide antibiotic with anti-Neisseria activity"
CSDB ID 47732
(all data & tools)
Compound ID:
14220
a-D-Manp-(1-1)-+ | Subst2-(1-2)-a-D-GlcpNA-(1-2)-Subst Subst = SMILES CN[C@H]6C(=O)N[C@@H]4Cc1ccc(cc1)Oc%11cc3cc(Oc2ccc(cc2Cl)C(O)C%10NC(=O)[C@H](NC(=O)[C@@H]3NC(=O)[C@@H](NC4=O)c5cc(cc(O)c5Cl)Oc7cc6ccc7O)c8cccc(c8)c9{1}c(O)cc(O)cc9[C@@H](C(=O)O)NC%10=O){2}c%11O; Subst2 = isolauric acid = SMILES CC(C)CCCCCCCC{1}C(=O)O
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Structure type:
oligomer ; 1730
Trivial name:
A40926
Compound class:
glycoside
Antimicrobial Agents and Chemotherapy
1987, "A40926, a new glycopeptide antibiotic with anti-Neisseria activity"
CSDB ID 47733
(all data & tools)
Compound ID:
14221
a-D-Manp6Ac-(1-1)-+ | Subst2-(1-2)-a-D-GlcpNA-(1-2)-Subst Subst = SMILES CN[C@H]6C(=O)N[C@@H]4Cc1ccc(cc1)Oc%11cc3cc(Oc2ccc(cc2Cl)C(O)C%10NC(=O)[C@H](NC(=O)[C@@H]3NC(=O)[C@@H](NC4=O)c5cc(cc(O)c5Cl)Oc7cc6ccc7O)c8cccc(c8)c9{1}c(O)cc(O)cc9[C@@H](C(=O)O)NC%10=O){2}c%11O; Subst2 = isolauric acid = SMILES CC(C)CCCCCCCC{1}C(=O)O
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Structure type:
oligomer ; 1772
Trivial name:
A40926
Compound class:
glycoside
Antimicrobial Agents and Chemotherapy
1987, "A40926, a new glycopeptide antibiotic with anti-Neisseria activity"
CSDB ID 47734
(all data & tools)
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