CHEBI:10696 - (3S)-3-hydroxy-L-aspartic acid

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ChEBI Name (3S)-3-hydroxy-L-aspartic acid
ChEBI ID CHEBI:10696
ChEBI ASCII Name (3S)-3-hydroxy-L-aspartic acid
Definition The (3S)-diastereomer of 3-hydroxy-L-aspartic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Related Structures
(3S)-3-hydroxy-L-aspartic acid has Substituent Group(s)
(3S)-3-hydroxy-L-aspartic acid residue
Mass : 131.08684
Formula : C4H5NO4
41121
(3S)-3-hydroxy-L-aspartic acid is a Structural Derivative of
ammonia
Mass : 17.03056
Formula : H3N
16134 		L-aspartic acid
Mass : 133.10270
Formula : C4H7NO4 C4H7NO4
17053 		proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
(3S)-3-hydroxy-L-aspartic acid is a Conjugate Acid of
(3S)-3-hydroxy-L-aspartate(1-)
Mass : 148.09410
Formula : C4H6NO5
57251 		(3S)-3-hydroxy-L-aspartate(2-)
Mass : 147.08624
Formula : C4H5NO5
17838
(3S)-3-hydroxy-L-aspartic acid is a Enantiomer of
(3R)-3-hydroxy-D-aspartic acid
Mass : 149.10210
Formula : C4H7NO5
60897
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