Substrate

Bibliography

Biblio print

Tree Display

AceDB Schema

XML Display

Feedback

Substrate Report for: 2,3-Dihydroxybenzoylserine

To obtain iron, many pathogenic bacteria have evolved metabolic pathways to synthesize, transport, and process small molecules, termed siderophores. Enterobactin is an iron-binding cyclic trimer of 2,3-dihydroxy-N-benzoyl-L-serine. Enterobactin is linearized by IroE in the periplasm, and hydrolysed in 3 monomers by Fes liberating Fe in the cytoplasm.


General
Type
Chemical_Nomenclature (2S)-2-[(2,3-dihydroxybenzoyl)amino]-3-hydroxypropanoic acid
Canonical SMILES C1=CC(=C(C(=C1)O)O)C(=O)NC(CO)C(=O)O
InChI InChI=1S/C10H11NO6/c12-4-6(10(16)17)11-9(15)5-2-1-3-7(13)8(5)14/h1-3,6,12-14H,4H2,(H,11,15)(H,16,17)/t6-/m0/s1
InChIKey VDTYHTVHFIIEIL-LURJTMIESA-N
Other name(s) 2,3-di-hydroxy-N-benzoyl-serine ; N-(2,3-dihydroxybenzoyl)-L-serine ; 2,3,-DIHYDROXYBENZOYLSERINE ; 2,3-Dihydroxy-N-benzoyl-L-serine ; L-Serine, N-(2,3-dihydroxybenzoyl)-
________________________________________________________________________________________________
MW|241.19
Formula|C10H11NO6
CAS_number|7724-78-9
PubChem|151483
UniChem|VDTYHTVHFIIEIL-LURJTMIESA-N
IUPHAR|
Wikipedia|

Target
Families | 2,3-Dihydroxybenzoylserine ligand of proteins in family: A85-IroE-IroD-Fes-Yiel
Stucture | 2 structures: 3C8D, 3C8H
Protein | shifl-FES

References:
Search PubMed for references concerning: 2,3-Dihydroxybenzoylserine

No Reference