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
Target
Families : A85-IroE-IroD-Fes-Yiel
References
No reference