Reaction participants Show >> << Hide
- Name help_outline ATP Identifier CHEBI:30616 (Beilstein: 3581767) help_outline Charge -4 Formula C10H12N5O13P3 InChIKeyhelp_outline ZKHQWZAMYRWXGA-KQYNXXCUSA-J SMILEShelp_outline Nc1ncnc2n(cnc12)[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O 2D coordinates Mol file for the small molecule Search links Involved in 1,280 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline streptidine Identifier CHEBI:184376 Charge 2 Formula C8H20N6O4 InChIKeyhelp_outline MSXMXWJPFIDEMT-FAEUDGQSSA-P SMILEShelp_outline NC(=[NH2+])N[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](NC(N)=[NH2+])[C@@H]1O 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 6-O-adenylylstreptidine Identifier CHEBI:184375 Charge 1 Formula C18H31N11O10P InChIKeyhelp_outline HNYZZTVCUNXAIP-BKCFTUSJSA-O SMILEShelp_outline C([C@H]1O[C@H]([C@@H]([C@@H]1O)O)N2C3=C(C(=NC=N3)N)N=C2)OP(O[C@H]4[C@@H]([C@H]([C@@H]([C@H]([C@@H]4O)O)NC(=[NH2+])N)O)NC(N)=[NH2+])(=O)[O-] 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline diphosphate Identifier CHEBI:33019 (Beilstein: 185088) help_outline Charge -3 Formula HO7P2 InChIKeyhelp_outline XPPKVPWEQAFLFU-UHFFFAOYSA-K SMILEShelp_outline OP([O-])(=O)OP([O-])([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 1,129 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:69544 | RHEA:69545 | RHEA:69546 | RHEA:69547 | |
|---|---|---|---|---|
| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
| UniProtKB help_outline |
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Publications
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Rescue of the streptomycin antibiotic activity by using streptidine as a 'decoy acceptor' for the aminoglycoside-inactivating enzyme adenyl transferase.
Latorre M., Penalver P., Revuelta J., Asensio J.L., Garcia-Junceda E., Bastida A.
The use of streptidine as a "decoy acceptor" allows the antibiotic activity of streptomycin to recover against the Escherichia coli strain overexpressing the aminoglycoside-modifying enzyme 6-O-adenyl transferase.
Chem. Commun. (Camb.) 27:2829-2831(2007) [PubMed] [EuropePMC]