2,3-Diaminopropionic acid
 | |
| Names | |
|---|---|
| IUPAC name
(2S)-2,3-Diaminopropanoic acid | |
| Identifiers | |
| 4033-39-0 | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:16303 |
| KEGG | C03401 |
| PubChem | 97328 |
| UNII | JE1TUV83JA |
| |
| |
| Properties | |
| C3H8N2O2 | |
| Molar mass | 104.11 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
2,3-Diaminopropionic acid (2,3-diaminopropionate) is a non-proteinogenic amino acid found in certain secondary metabolites, including zwittermicin A[1] and tuberactinomycin.[2]
Biosynthesis
2,3-Diaminopropionate is formed by the pyridoxal phosphate (PLP) mediated amination of serine.
Biosynthesis of L-2,3 Diaminopropionate
References
- ↑ Rogers EW, Molinski TF (February 2007). "Asymmetric synthesis of diastereomeric diaminoheptanetetraols. A proposal for the configuration of (+)-zwittermicin a". Org. Lett. 9 (3): 437–40. doi:10.1021/ol062804a. PMC 2729442
. PMID 17249781. - ↑ Michael G. Thomas (2003). "ADeciphering Tuberactinomycin Biosynthesis: Isolation, Sequencing, and Annotation of the Viomycin Biosynthetic Gene Cluster". Antimicrob Agents Chemother. 47 (9): 2823–2830. doi:10.1128/AAC.47.9.2823-2830.2003. PMC 182626. PMID 12936980.
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