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discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
12/28 - 12/31
for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
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Escherichia coli K-12 substr. MG1655 Compound: 5-aminolevulinate

Systematic Name: 5-amino-4-oxo-pentanoate

Synonyms: 5-amino-4-oxopentanoate, 5-amino-4-oxo-pentanoic acid, 5-amino-levulinic acid, 5-amino-4-oxopentanoic acid, δ-aminolevulinate, 5-aminolevulinic acid, 5-amino-levulinate, ALA, δ-aminolevulinic acid

Chemical Formula: C5H9NO3

Molecular Weight: 131.13 Daltons

Monoisotopic Molecular Weight: 131.0582431604 Daltons

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

InChI: InChI=1S/C5H9NO3/c6-3-4(7)1-2-5(8)9/h1-3,6H2,(H,8,9)

InChIKey: InChIKey=ZGXJTSGNIOSYLO-UHFFFAOYSA-N

Unification Links: CAS:106-60-5 , ChEBI:356416 , HMDB:HMDB01149 , IAF1260:34963 , KEGG:C00430 , MetaboLights:MTBLC356416 , PubChem:7048523

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -112.89

Reactions known to consume the compound:

tetrapyrrole biosynthesis I (from glutamate) :
2 5-aminolevulinate → porphobilinogen + H+ + 2 H2O

Reactions known to produce the compound:

tetrapyrrole biosynthesis I (from glutamate) :
glutamate-1-semialdehyde → 5-aminolevulinate


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 Dec 21, 2014, BIOCYC13B.