Record Information
Version1.0
StatusDetected and Quantified
Creation Date2021-11-17 23:34:30 UTC
Update Date2024-10-09 19:49:54 UTC
Metabolite IDMMDBc0029611
Metabolite Identification
Common NameL-D-1-Pyrroline-5-carboxylic acid
Description(S)-1-Pyrroline-5-carboxylate Pyrroline 5-carboxylate is an enamine or an imino acid that forms on spontaneous dehydration of L-glutamate γ-semialdehyde in aqueous solutions. The stereoisomer (S)-1-Pyrroline-5-carboxylate is an intermediate in glutamate metabolism, in arginine degradation and in proline biosynthesis and degradation and it can be converted to or be formed from the three amino acids L-glutamate, L-ornithine and L-proline. In particular, it is synthesized with the oxidation of proline by pyrroline-5-carboxylate reductase 1 (EC 1.5.1.2, PYCR1) or by proline dehydrogenase (EC 1.5.99.8, PRODH) and it is hydrolyzed to L-glutamate by delta-1-pyrroline-5-carboxylate dehydrogenase (EC 1.5.1.12, ALDH4A1). It is also one of the few metabolites that can be a precursor to other metabolites of both the urea cycle and the tricarboxylic acid (TCA) cycle.
Structure
SynonymsNot Available
Molecular FormulaC5H7NO2
Average Mass113.1146
Monoisotopic Mass113.047678473
IUPAC NameNot Available
Traditional NameNot Available
CAS Registry Number2906-39-0
SMILESNot Available
InChI Identifier
InChI=1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h3-4H,1-2H2,(H,7,8)
InChI KeyDWAKNKKXGALPNW-UHFFFAOYSA-N