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discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
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Escherichia coli K-12 substr. MG1655 Compound Class: 2-aminobutanoate

Synonyms: DL-a-amino-N-butyric acid, 2-aminobutyric acid, 2-amino-n-butyric Acid, butyrine, α-aminobutyric acid, D,L-α-amino-N-butyrate, 2-aminobutyrate

Superclasses: an amine

Chemical Formula: C4H9NO2

Instances:
(R)-2-aminobutanoate ,
(S)-2-aminobutanoate

Molecular Weight: 103.12 Daltons

Monoisotopic Molecular Weight: 103.0633285383 Daltons

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

InChI: InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)

Unification Links: CAS:2835-81-6 , ChEBI:35621 , PubChem:517460

In Reactions of unknown directionality:

Not in pathways:
an aminated amino group acceptor + 2-oxobutanoate = 2-aminobutanoate + a deaminated amino group acceptor

Enzymes inhibited by 2-aminobutanoate, sorted by the type of inhibition, are:

Inhibitor (Competitive) of: homoserine kinase [Theze74b, Burr76]

In Growth Media: PMA nitrogen source test + 2-aminobutyrate

Credits:
Imported from MetaCyc 16-May-2012 by Paley S , SRI International


References

Burr76: Burr B, Walker J, Truffa-Bachi P, Cohen GN (1976). "Homoserine kinase from Escherichia coli K12." Eur J Biochem 1976;62(3);519-26. PMID: 177283

Theze74b: Theze J, Kleidman L, St Girons I (1974). "Homoserine kinase from Escherichia coli K-12: properties, inhibition by L-threonine, and regulation of biosynthesis." J Bacteriol 1974;118(2);577-81. PMID: 4364023


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by SRI International Pathway Tools version 18.5 on Sun Nov 23, 2014, biocyc13.