CHEBI:497734 - L-thialysine

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ChEBI Name L-thialysine
ChEBI ID CHEBI:497734
ChEBI ASCII Name L-thialysine
Definition A cysteine derivative that is the S-(2-aminoethyl) analogue of L-cysteine; reported to have cytotoxic effects.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:45515
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): protein synthesis inhibitor
A compound, usually an anti-bacterial agent or a toxin, which inhibits the synthesis of a protein.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
EC 5.4.3.2 (lysine 2,3-aminomutase) inhibitor
An EC 5.4.3.* (intramolecular transferase transferring amino groups) inhibitor that interferes with the action of lysine 2,3-aminomutase (EC 5.4.3.2).
Related Structures
L-thialysine is a Functional Parent of
N-acetyl-L-thialysine
Mass : 206.260
Formula : C7H14N2O3S
156139
L-thialysine is a Structural Derivative of
ammonia
Mass : 17.03056
Formula : H3N
16134 		L-cysteine
Mass : 121.15800
Formula : C3H7NO2S
17561 		cysteine
Mass : 121.15922
Formula : C3H7NO2S
15356 		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.
L-thialysine is a Conjugate Base of
L-thialysinium
Mass : 165.230
156132
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