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Record Information
Version	2.0
Creation Date	2015-09-08 17:49:55 -0600
Update Date	2016-09-13 16:35:42 -0600
Secondary Accession Numbers	ECMDB24181
Identification
Name:	S-ureidoglycine
Description	S-ureidoglycine aminohydrolase (gene name: allE; EC Number: 3.5.3.26) is an enzyme that catalyses the chemical reaction S-ureidoglycine + H2O <=> S-ureidoglycolate + ammonium in E. coli (BioCyc).
Structure	MOLSDF3D-SDFPDBSMILESInChI View 3D Structure × Structure for #<Compound:0xa4e23854> Close
Synonyms:	Value Source (2S)-Amino(carbamoylamino)acetic acid ChEBI (2S)-Amino(carbamoylamino)ethanoic acid ChEBI (2S)-Ureidoglycine ChEBI (2S)-Amino(carbamoylamino)acetate Generator (2S)-Amino(carbamoylamino)ethanoate Generator
Chemical Formula:
Weight:	Average: Not Available Monoisotopic: Not Available
InChI Key:	Not Available
InChI:	Not Available
CAS number:	Not Available
IUPAC Name:	(2S)-2-amino-2-(carbamoylamino)acetic acid
Traditional IUPAC Name:	(S)-2-ureidoglycine
SMILES:	Not Available
Chemical Taxonomy
Description	belongs to the class of organic compounds known as n-carbamoyl-alpha amino acids. N-carbamoyl-alpha amino acids are compounds containing an alpha amino acid which bears an carbamoyl group at its terminal nitrogen atom.
Kingdom	Organic compounds
Super Class	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Sub Class	Amino acids, peptides, and analogues
Direct Parent	N-carbamoyl-alpha amino acids
Alternative Parents	Ureas Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Substituents	N-carbamoyl-alpha-amino acid Urea Carbonic acid derivative Monocarboxylic acid or derivatives Carboxylic acid Organic nitrogen compound Organic oxygen compound Organopnictogen compound Organic oxide Hydrocarbon derivative Organooxygen compound Organonitrogen compound Primary aliphatic amine Carbonyl group Aliphatic acyclic compound
Molecular Framework	Aliphatic acyclic compounds
External Descriptors	2-ureidoglycine (CHEBI:59945 )
Physical Properties
State:	Not Available
Charge:	0
Melting point:	Not Available
Experimental Properties:	Property Value Source
Predicted Properties	Property Value Source Water Solubility 58.2 g/L ALOGPS logP -3.3 ALOGPS logP -4.3 ChemAxon logS -0.36 ALOGPS pKa (Strongest Acidic) 1.43 ChemAxon pKa (Strongest Basic) 7.41 ChemAxon Physiological Charge 0 ChemAxon Hydrogen Acceptor Count 4 ChemAxon Hydrogen Donor Count 4 ChemAxon Polar Surface Area 118.44 Ų ChemAxon Rotatable Bond Count 2 ChemAxon Refractivity 26.98 m³·mol⁻¹ ChemAxon Polarizability 11.21 ų 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:	Allantoic acid + Water + 2 Hydrogen ion > Carbon dioxide + Ammonium + S-ureidoglycine S-ureidoglycine + Water > Ammonium + (S)-Ureidoglycolic acid
SMPDB Pathways:	allantoin degradation (anaerobic) PW002050 glycolate and glyoxylate degradation PW000827
KEGG Pathways:	Not Available
EcoCyc Pathways:	Not Available
Concentrations
	Not Available
Spectra
Spectra:	Not Available
References
References:	Not Available
Synthesis Reference:	Not Available
Material Safety Data Sheet (MSDS)	Not Available
Links
External Links:	Resource Link CHEBI ID 59945 HMDB ID Not Available Pubchem Compound ID 45479615 Kegg ID C02091 ChemSpider ID Not Available Wikipedia ID Not Available BioCyc ID Not Available

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