Record Information |
---|
Version | 2.0 |
---|
Creation Date | 2015-09-08 17:50:01 -0600 |
---|
Update Date | 2015-09-14 16:46:31 -0600 |
---|
Secondary Accession Numbers | |
---|
Identification |
---|
Name: | γ-L-glutamyl 5-phosphate |
---|
Description | gamma-L-Glutamyl 5-phosphate is an intermediate in L-proline biosynthesis I pathway in E.coli. It is a product for the enzyme gamma-glutamyl kinase which catalyzes the reaction L-glutamate + ATP -> gamma-L-glutamyl 5-phosphate + ADP. It is also the substrate for the enzyme glutamate-5-semialdehyde dehydrogenase which catalyzes the reaction gamma-L-glutamyl 5-phosphate + NADPH + H+ -> L-glutamate-5-semialdehyde + NADP+ + phosphate (BioCyc compound: L-GLUTAMATE-5-P). |
---|
Structure | |
---|
Synonyms: | - γ-L-glutamyl 5-phosphoric acid
|
---|
Chemical Formula: | C5H8NO7P |
---|
Weight: | Average: 225.094 Monoisotopic: 225.004935759 |
---|
InChI Key: | PJRXVIJAERNUIP-VKHMYHEASA-L |
---|
InChI: | InChI=1S/C5H10NO7P/c6-3(5(8)9)1-2-4(7)13-14(10,11)12/h3H,1-2,6H2,(H,8,9)(H2,10,11,12)/p-2/t3-/m0/s1 |
---|
CAS number: | Not Available |
---|
IUPAC Name: | (2S)-2-amino-5-(hydrogen phosphonatooxy)-5-oxopentanoate |
---|
Traditional IUPAC Name: | (2S)-2-amino-5-(hydrogen phosphonatooxy)-5-oxopentanoate |
---|
SMILES: | [H][C@](N)(CCC(=O)OP(O)([O-])=O)C([O-])=O |
---|
Chemical Taxonomy |
---|
Description | belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
---|
Kingdom | Organic compounds |
---|
Super Class | Organic acids and derivatives |
---|
Class | Carboxylic acids and derivatives |
---|
Sub Class | Amino acids, peptides, and analogues |
---|
Direct Parent | Glutamic acid and derivatives |
---|
Alternative Parents | |
---|
Substituents | - Glutamic acid or derivatives
- Alpha-amino acid
- L-alpha-amino acid
- Acyl monophosphate
- Acyl phosphate
- Dicarboxylic acid or derivatives
- Organic phosphoric acid derivative
- Fatty acid
- Carboxylic acid salt
- Amino acid
- Carboxylic acid
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Hydrocarbon derivative
- Primary aliphatic amine
- Organic oxide
- Organic nitrogen compound
- Organopnictogen compound
- Carbonyl group
- Amine
- Organic oxygen compound
- Organic salt
- Organic anion
- Aliphatic acyclic compound
|
---|
Molecular Framework | Aliphatic acyclic compounds |
---|
External Descriptors | |
---|
Physical Properties |
---|
State: | Not Available |
---|
Charge: | -2 |
---|
Melting point: | Not Available |
---|
Experimental Properties: | |
---|
Predicted Properties | |
---|
Biological Properties |
---|
Cellular Locations: | Cytoplasm |
---|
Reactions: | |
---|
SMPDB Pathways: | |
---|
KEGG Pathways: | Not Available |
---|
EcoCyc Pathways: | Not Available |
---|
Concentrations |
---|
| Not Available |
---|
Spectra |
---|
Spectra: | |
---|
References |
---|
References: | Not Available |
---|
Synthesis Reference: | Not Available |
---|
Material Safety Data Sheet (MSDS) | Not Available |
---|
Links |
---|
External Links: | Resource | Link |
---|
CHEBI ID | 58274 | HMDB ID | Not Available | Pubchem Compound ID | Not Available | Kegg ID | Not Available | ChemSpider ID | Not Available | Wikipedia ID | Not Available | BioCyc ID | Not Available |
|
---|