P. aeruginosa Metabolome Database: L-Glutamic-gamma-semialdehyde (PAMDB000331)

Identification Taxonomy Physical Properties Biological Properties Spectra Concentrations Links References Enzymes Transporters

Proteins (3280)

Record Information

Version

1.0

Update Date

1/22/2018 11:54:54 AM

Metabolite ID

PAMDB000331

Identification

Name:

L-Glutamic-gamma-semialdehyde

Description:

Glutamic gamma-semialdehyde is the metabolic precursor for proline biosynthesis. The conversion from L-Glutamate, an ATP- and NADPH-dependent reaction, is catalyzed by the enzyme Delta-1-pyrroline-5-carboxylate synthetase (P5CS) (OMIM 138250). L-Glutamic-gamma-semialdehyde can also be converted to or be formed from the amino acids L-ornithine (EC 2.6.1.13) and L-proline (EC 1.5.99.8 and EC 1.5.1.2). It is also one of the few metabolites that can be a precursor to other metabolites of both the urea cycle and the citric acid cycle (BioCyc)

Structure

🔍MOL SDF PDB SMILES InChI View Structure

Synonyms:

Glutamate-semialdehyde
Glutamic γ-semialdehyde
Glutamic acid-semialdehyde
Glutamic g-semialdehyde
Glutamic gamma-semialdehyde
Glutamic γ-semialdehyde
L-Glutamate 5-semialdehyde
L-Glutamate g-semialdehyde
L-Glutamate gamma-semialdehyde
L-Glutamate γ-semialdehyde
L-Glutamate-5-semialdehyde
L-Glutamic acid 5-semialdehyde
L-Glutamic acid g-semialdehyde
L-Glutamic acid gamma-semialdehyde
L-Glutamic acid γ-semialdehyde
L-Glutamic acid-5-semialdehyde
L-Glutamic-g-semialdehyde
L-Glutamic-gamma-semialdehyde
L-Glutamic-γ-semialdehyde

Chemical Formula:

C₅H₉NO₃

Average Molecular Weight:

131.1299

Monoisotopic Molecular Weight:

131.058243159

InChI Key:

KABXUUFDPUOJMW-BYPYZUCNSA-N

InChI:

InChI=1S/C5H9NO3/c6-4(5(8)9)2-1-3-7/h3-4H,1-2,6H2,(H,8,9)/t4-/m0/s1

CAS number:

496-92-4

IUPAC Name:

(2S)-2-amino-5-oxopentanoic acid

Traditional IUPAC Name:

4-carboxy-4-aminobutanal

SMILES:

N[C@@H](CCC=O)C(O)=O

Chemical Taxonomy

Taxonomy Description

This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

L-alpha-amino acids

Alternative Parents

Substituents

L-alpha-amino acid
Amino fatty acid
Fatty acyl
Fatty acid
Alpha-hydrogen aldehyde
Monocarboxylic acid or derivatives
Carboxylic acid
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Amine
Aldehyde
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

glutamic semialdehyde (CHEBI:17232 )

Physical Properties

State:

Solid

Charge:

Melting point:

Not Available

Experimental Properties:

Property	Value	Source

Predicted Properties

Property	Value	Source
Water Solubility	144.0 mg/mL	ALOGPS
logP	-2.6	ALOGPS
logP	-3.4	ChemAxon
logS	0.04	ALOGPS
pKa (Strongest Acidic)	2.12	ChemAxon
pKa (Strongest Basic)	9.11	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	80.39 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	30.36 m³·mol^-1	ChemAxon
Polarizability	12.56 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	1	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Biological Properties

Cellular Locations:

Cytoplasm

Reactions:

Pathways:

Arginine and proline metabolism pae00330
Metabolic pathways pae01100

Spectra

Spectra:

Spectrum Type	Description	Splash Key
GC-MS	GC-MS Spectrum - GC-MS	Not Available
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-02a9-9700000000-ffc8c81a881bac7a0ca7	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00kr-9100000000-7061d8b19402303b61af	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4l-9000000000-fa50d608bfaec666722d	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-001i-1900000000-485c1c464e6d065cb4ac	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-01q9-7900000000-cd2ef70374a324d28ee0	View in MoNA
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0006-9000000000-8685f6b3a1d6936c24c3	View in MoNA

References

References:

Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510
Keseler, I. M., Collado-Vides, J., Santos-Zavaleta, A., Peralta-Gil, M., Gama-Castro, S., Muniz-Rascado, L., Bonavides-Martinez, C., Paley, S., Krummenacker, M., Altman, T., Kaipa, P., Spaulding, A., Pacheco, J., Latendresse, M., Fulcher, C., Sarker, M., Shearer, A. G., Mackie, A., Paulsen, I., Gunsalus, R. P., Karp, P. D. (2011). "EcoCyc: a comprehensive database of Escherichia coli biology." Nucleic Acids Res 39:D583-D590. Pubmed: 21097882
van der Werf, M. J., Overkamp, K. M., Muilwijk, B., Coulier, L., Hankemeier, T. (2007). "Microbial metabolomics: toward a platform with full metabolome coverage." Anal Biochem 370:17-25. Pubmed: 17765195

Synthesis Reference:

Not Available

Material Safety Data Sheet (MSDS)

Not Available

Links

External Links:

Resource	Link
CHEBI ID	17232
HMDB ID	HMDB02104
Pubchem Compound ID	193305
Kegg ID	C01165
ChemSpider ID	167744
Wikipedia ID	Not Available
BioCyc ID	L-GLUTAMATE_GAMMA-SEMIALDEHYDE
EcoCyc ID	L-GLUTAMATE_GAMMA-SEMIALDEHYDE
Ligand Expo	ILG

L-Glutamic-gamma-semialdehyde (PAMDB000331)

Structure for L-Glutamic-gamma-semialdehyde (PAMDB000331)