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Thus, the two substrates of this enzyme are (R)-3-amino-2-methylpropanoate and pyruvate, whereas its two products are 2-methyl-3-oxopropanoate and L-alanine. This enzyme belongs to the family of transferases , specifically the transaminases , which transfer nitrogenous groups.
L-alanine is second only to L-leucine in rate of occurrence, accounting for 7.8% of the primary structure in a sample of 1,150 proteins. [5] The right-handed form, D -alanine, occurs in peptides in some bacterial cell walls [ 6 ] : 131 (in peptidoglycan ) and in some peptide antibiotics , and occurs in the tissues of many crustaceans and ...
In enzymology, a serine-pyruvate transaminase (EC 2.6.1.51) is an enzyme that catalyzes the chemical reaction. L-serine + pyruvate 3-hydroxypyruvate + L-alanine. Thus, the two substrates of this enzyme are L-serine and pyruvate, whereas its two products are 3-hydroxypyruvate and L-alanine.
L-phenylalanine + pyruvate phenylpyruvate + L-alanine Thus, the two substrates of this enzyme are L-phenylalanine and pyruvate , whereas its two products are phenylpyruvate and L-alanine . This enzyme belongs to the family of transferases , specifically the transaminases , which transfer nitrogenous groups.
^a EINECS for L-alanine ^a CID 602 from PubChem ^a CID 5950 from PubChem This page was last edited on 12 April 2023, at 11:37 (UTC). Text is available ...
Cysteic acid also known as 3-sulfo-l-alanine is the organic compound with the formula HO 3 SCH 2 CH(NH 2)CO 2 H. It is often referred to as cysteate, which near neutral pH takes the form − O 3 SCH 2 CH(NH 3 +)CO 2 −. It is an amino acid generated by oxidation of cysteine, whereby a thiol group is fully oxidized to a sulfonic acid/sulfonate ...
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L-aspartate L-alanine + CO 2. Hence, this enzyme has one substrate, L-aspartate, and two products, L-alanine and CO 2. This reaction is the basis of the industrial synthesis of L-alanine. [1] This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds.
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