Record Information
Version2.0
Creation Date2012-05-31 14:29:46 -0600
Update Date2015-09-13 12:56:14 -0600
Secondary Accession Numbers
  • ECMDB20143
Identification
Name:D-Galacturonate
DescriptionD-Galacturonic acid is a sugar acid, the oxidized form of D-galactose. It is the main component of pectin, in which it exists as the polymer polygalacturonic acid. -- Wikipedia
Structure
Thumb
Synonyms:
  • a-delta-Galactopyranuronate
  • a-delta-Galactopyranuronic acid
  • a-delta-Galacturonate
  • a-delta-Galacturonic acid
  • a-delta-Polygalacturonate
  • a-delta-Polygalacturonic acid
  • a-δ-Galactopyranuronate
  • a-δ-Galactopyranuronic acid
  • a-δ-Galacturonate
  • a-δ-Galacturonic acid
  • a-δ-Polygalacturonate
  • a-δ-Polygalacturonic acid
  • alpha-delta-Galactopyranuronate
  • Alpha-delta-galactopyranuronic acid
  • alpha-delta-Galacturonate
  • Alpha-delta-galacturonic acid
  • alpha-delta-Polygalacturonate
  • Alpha-delta-polygalacturonic acid
  • Calcium pectate
  • Calcium pectic acid
  • Calcium polygalacturonate
  • Calcium polygalacturonic acid
  • D-(+)-Galacturonate monohydrate
  • D-(+)-Galacturonic acid monohydrate
  • D-(+)-Galacturonic acid monohydric acid
  • D-Galactopyranuronate
  • D-Galactopyranuronic acid
  • D-galacturonan
  • D-Galacturonate
  • D-Galacturonate, homopolymer
  • D-Galacturonic acid
  • D-Galacturonic acid, homopolymer
  • D-galaturonate
  • D-Galaturonic acid
  • Delta-galacturonan
  • Delta-galacturonate
  • Delta-Galacturonic acid
  • DL-galacturonate
  • DL-galacturonic acid
  • Galacturonan
  • Galacturonate
  • Galacturonic acid
  • Galaturonate
  • Galaturonic acid
  • Hexuronate
  • Hexuronic acid
  • Pectate
  • Pectic acid
  • Poly(1,4-a-D-galacturonate)
  • Poly(1,4-a-D-galacturonic acid)
  • Poly(1,4-a-delta-galacturonate)
  • Poly(1,4-a-delta-galacturonic acid)
  • Poly(1,4-a-δ-galacturonate)
  • Poly(1,4-a-δ-galacturonic acid)
  • Poly(1,4-alpha-D-galacturonate)
  • Poly(1,4-alpha-D-galacturonic acid)
  • Poly(1,4-alpha-delta-galacturonate)
  • Poly(1,4-alpha-delta-galacturonic acid)
  • Poly(1,4-α-D-galacturonate)
  • Poly(1,4-α-D-galacturonic acid)
  • Poly(1,4-α-δ-galacturonate)
  • Poly(1,4-α-δ-galacturonic acid)
  • Polygalacturonate
  • Polygalacturonic acid
  • Sodium pectate
  • Sodium pectic acid
  • Sulfated polygalacturonate
  • Sulfated polygalacturonic acid
  • Sulphated polygalacturonate
  • Sulphated polygalacturonic acid
  • α-δ-Galactopyranuronate
  • α-δ-Galactopyranuronic acid
  • α-δ-Galacturonate
  • α-δ-Galacturonic acid
  • α-δ-Polygalacturonate
  • α-δ-Polygalacturonic acid
  • δ-Galacturonan
  • δ-Galacturonate
  • δ-Galacturonic acid
Chemical Formula:C6H10O7
Weight:Average: 194.1394
Monoisotopic: 194.042652674
InChI Key:IAJILQKETJEXLJ-RSJOWCBRSA-N
InChI:InChI=1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h1-5,8-11H,(H,12,13)/t2-,3+,4+,5-/m0/s1
CAS number:685-73-4
IUPAC Name:(2S,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoic acid
Traditional IUPAC Name:aldehydo-D-galacturonic acid
SMILES:O[C@@H](C=O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O
Chemical Taxonomy
Description belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentGlucuronic acid derivatives
Alternative Parents
Substituents
  • Glucuronic acid or derivatives
  • Hexose monosaccharide
  • Medium-chain hydroxy acid
  • Medium-chain fatty acid
  • Beta-hydroxy acid
  • Hydroxy fatty acid
  • Monosaccharide
  • Fatty acyl
  • Hydroxy acid
  • Fatty acid
  • Alpha-hydroxy acid
  • Beta-hydroxy aldehyde
  • Alpha-hydroxyaldehyde
  • Secondary alcohol
  • Polyol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Aldehyde
  • Carbonyl group
  • Alcohol
  • Organic oxide
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Physical Properties
State:Solid
Charge:-1
Melting point:166 °C
Experimental Properties:
PropertyValueSource
Predicted Properties
PropertyValueSource
Water Solubility100 g/LALOGPS
logP-2.3ALOGPS
logP-3.2ChemAxon
logS-0.29ALOGPS
pKa (Strongest Acidic)3.24ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area135.29 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity37.21 m³·mol⁻¹ChemAxon
Polarizability16.23 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Biological Properties
Cellular Locations:Cytoplasm
Reactions:
SMPDB Pathways:
Starch and sucrose metabolismPW000941 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG Pathways:
  • ABC transporters ec02010
  • Amino sugar and nucleotide sugar metabolism ec00520
  • Ascorbate and aldarate metabolism ec00053
  • Pentose and glucuronate interconversions ec00040
  • Starch and sucrose metabolism ec00500
EcoCyc Pathways:
Concentrations
Not Available
Spectra
Spectra:
Spectrum TypeDescriptionSplash Key
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-000i-9800000000-1d25ab641e968717daf1View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (5 TMS) - 70eV, Positivesplash10-00n0-3139450000-1762a4c61557c689a607View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 10V, Positive (Annotated)splash10-03e9-0900000000-04b6c8cb4b4b2c077202View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 25V, Positive (Annotated)splash10-0lk9-9700000000-4260c2e124c927041b62View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Quattro_QQQ 40V, Positive (Annotated)splash10-004i-9000000000-650b5bb9db964b1c3e87View in MoNA
LC-MS/MSLC-MS/MS Spectrum - , negativesplash10-000i-9410000000-180d0e747dbcb5b21b01View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-056s-2900000000-86606b8382ffe403bc8eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-9500000000-af67bc97552641417beeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a4i-9100000000-205a7cff1e298283a080View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-05p9-9700000000-ee070fab487c9f3e49b7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a4r-9400000000-284825e422ba9585f17bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4i-9100000000-64d4f9d758e2a4eeba68View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-01y5-7900000000-df218a4e340a0ff668c1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03kl-9100000000-d22d4d2644d77203331dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-08fu-9000000000-93301767b758d212114fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00fr-9300000000-77aa1619935fe785e397View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a6r-9000000000-da4be7e32a829503c021View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a6r-9000000000-c1c9308cd925f43d015fView in MoNA
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR13C NMR SpectrumNot AvailableView in JSpectraViewer
1D NMR1H NMR SpectrumNot AvailableView in JSpectraViewer
2D NMR[1H,13C] 2D NMR SpectrumNot AvailableView in JSpectraViewer
References
References:
  • Hommes FA, Varghese M: High-performance liquid chromatography of urinary oligosaccharides in the diagnosis of glycoprotein degradation disorders. Clin Chim Acta. 1991 Dec 16;203(2-3):211-24. Pubmed: 1777982
  • 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
  • Winder, C. L., Dunn, W. B., Schuler, S., Broadhurst, D., Jarvis, R., Stephens, G. M., Goodacre, R. (2008). "Global metabolic profiling of Escherichia coli cultures: an evaluation of methods for quenching and extraction of intracellular metabolites." Anal Chem 80:2939-2948. Pubmed: 18331064
  • Wu AM, Song SC, Chen YY, Gilboa-Garber N: Defining the carbohydrate specificities of aplysia gonad lectin exhibiting a peculiar D-galacturonic acid affinity. J Biol Chem. 2000 May 12;275(19):14017-24. Pubmed: 10799474
Synthesis Reference:Not Available
Material Safety Data Sheet (MSDS)Download (PDF)
External Links:
ResourceLink
CHEBI ID12952
HMDB IDHMDB03363
Pubchem Compound ID439215
Kegg IDC00333
ChemSpider ID76444
Wikipedia IDD-Galacturonic acid
BioCyc IDD-GALACTURONATE
EcoCyc IDD-GALACTURONATE
Ligand ExpoDGU

Enzymes

General function:
Involved in glucuronate isomerase activity
Specific function:
D-glucuronate = D-fructuronate
Gene Name:
uxaC
Uniprot ID:
P0A8G3
Molecular weight:
53987
Reactions
D-glucuronate = D-fructuronate.
D-galacturonate = D-tagaturonate.

Transporters

General function:
Involved in transporter activity
Specific function:
Aldohexuronate transport system
Gene Name:
exuT
Uniprot ID:
P0AA78
Molecular weight:
51571
General function:
Involved in transporter activity
Specific function:
Non-specific porin
Gene Name:
ompN
Uniprot ID:
P77747
Molecular weight:
41220
General function:
Involved in transporter activity
Specific function:
Uptake of inorganic phosphate, phosphorylated compounds, and some other negatively charged solutes
Gene Name:
phoE
Uniprot ID:
P02932
Molecular weight:
38922
General function:
Involved in transporter activity
Specific function:
OmpF is a porin that forms passive diffusion pores which allow small molecular weight hydrophilic materials across the outer membrane. It is also a receptor for the bacteriophage T2
Gene Name:
ompF
Uniprot ID:
P02931
Molecular weight:
39333
General function:
Involved in transporter activity
Specific function:
Forms passive diffusion pores which allow small molecular weight hydrophilic materials across the outer membrane
Gene Name:
ompC
Uniprot ID:
P06996
Molecular weight:
40368