| Record Information |
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| Version | 2.0 |
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| Creation Date | 2012-07-30 14:55:05 -0600 |
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| Update Date | 2015-06-03 17:20:59 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | L-Alanyl-D-glutamate |
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| Description | L-alanine-D-glutamate is a dipeptide. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. It is a dipeptide that is a component of the bacterial cell wall. It is a substrate of Alanyl-glutamate epimerase which catalyzes the epimerization of L-Ala-D-Glu to L-Ala-L- Glu and has a role in the recycling of the murein peptide, of which L-Ala-D-Glu is a component. This enzyme also able to catalyze the reverse reaction. |
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| Structure | |
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| Synonyms: | - L-Ala-γ-D-Glu
- L-Ala-g-D-glu
- L-Ala-gamma-D-Glu
- L-Ala-γ-D-glu
- L-alanine-D-glutamate
- L-Alanine-D-glutamic acid
- L-Alanyl-D-glutamic acid
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| Chemical Formula: | C8H13N2O5 |
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| Weight: | Average: 217.1992
Monoisotopic: 217.082446536 |
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| InChI Key: | VYZAGTDAHUIRQA-UHFFFAOYSA-M |
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| InChI: | InChI=1S/C8H14N2O5/c1-4(9)7(13)10-5(8(14)15)2-3-6(11)12/h4-5H,2-3,9H2,1H3,(H,10,13)(H,11,12)(H,14,15)/p-1 |
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| CAS number: | Not Available |
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| IUPAC Name: | 2-[(2-amino-1-hydroxypropylidene)amino]pentanedioic acid |
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| Traditional IUPAC Name: | 2-[(2-amino-1-hydroxypropylidene)amino]pentanedioic acid |
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| SMILES: | CC(N)C(O)=NC(CCC([O-])=O)C(O)=O |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. |
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| Kingdom | Organic compounds |
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| Super Class | Organic acids and derivatives |
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| Class | Carboxylic acids and derivatives |
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| Sub Class | Amino acids, peptides, and analogues |
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| Direct Parent | Dipeptides |
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| Alternative Parents | |
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| Substituents | - Alpha-dipeptide
- Glutamic acid or derivatives
- N-acyl-alpha-amino acid
- N-acyl-alpha amino acid or derivatives
- Alpha-amino acid amide
- Alanine or derivatives
- Alpha-amino acid or derivatives
- Dicarboxylic acid or derivatives
- Fatty acid
- Amino acid or derivatives
- Carboxamide group
- Amino acid
- Secondary carboxylic acid amide
- Carboxylic acid
- Organonitrogen compound
- Organic oxygen compound
- Organic oxide
- Primary aliphatic amine
- Organopnictogen compound
- Organic nitrogen compound
- Carbonyl group
- Organooxygen compound
- Primary amine
- Amine
- Hydrocarbon derivative
- Aliphatic acyclic compound
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| Molecular Framework | Aliphatic acyclic compounds |
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| External Descriptors | Not Available |
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| Physical Properties |
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| State: | Not Available |
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| Charge: | -1 |
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| Melting point: | Not Available |
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| Experimental Properties: | |
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| Predicted Properties | |
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| Biological Properties |
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| Cellular Locations: | Cytoplasm |
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| Reactions: | |
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| SMPDB Pathways: | Not Available |
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| KEGG Pathways: | Not Available |
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| EcoCyc Pathways: | Not Available |
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| Concentrations |
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| Not Available |
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| Spectra |
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| Spectra: | |
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| References |
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| References: | Not Available |
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| Synthesis Reference: | Not Available |
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| Material Safety Data Sheet (MSDS) | Not Available |
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| Links |
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| External Links: | |
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