MetaCyc Compound: (2-aminoethyl)phosphonate

Synonyms: (2-aminoethane)phosphonate, ciliatine, 2-aminoethylphosphonate, 2-AEPn, 2-aminoethylphosphonic acid, phosphonoethylamine

Superclasses: an organophosphorus compoundan organophosphonatean aminoalkylphosphonate

Chemical Formula: C2H8NO3P

Molecular Weight: 125.06 Daltons

Monoisotopic Molecular Weight: 126.0320046704 Daltons

(2-aminoethyl)phosphonate compound structure

SMILES: C(CP([O-])(O)=O)[N+]

InChI: InChI=1S/C2H8NO3P/c3-1-2-7(4,5)6/h1-3H2,(H2,4,5,6)


Unification Links: ChEBI:57418, HMDB:HMDB11747, KEGG:C03557, MetaboLights:MTBLC57418, PubChem:5245507

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -128.84103Inferred by computational analysis [Latendresse13]

Reactions known to consume the compound:

2-aminoethylphosphonate degradation III :
(2-aminoethyl)phosphonate + 2-oxoglutarate + oxygen → (2-amino-1-hydroxyethyl)phosphonate + succinate + CO2

Reactions known to produce the compound:

2-aminoethylphosphonate biosynthesis :
phosphonoacetaldehyde + an aminated amino group donor → (2-aminoethyl)phosphonate + a deaminated amino group donor

Reactions known to both consume and produce the compound:

2-aminoethylphosphonate degradation I , 2-aminoethylphosphonate degradation II :
pyruvate + (2-aminoethyl)phosphonate ↔ L-alanine + phosphonoacetaldehyde

In Transport reactions:
an aminoalkylphosphonate[periplasm] + ATP + H2O → an aminoalkylphosphonate[cytosol] + ADP + phosphate + H+

This compound has been characterized as an alternative substrate of the following enzymes: aminoalkylphosphonate N-acetyltransferase


Latendresse13: Latendresse M. (2013). "Computing Gibbs Free Energy of Compounds and Reactions in MetaCyc."

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Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
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