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β-N [EC 3.2.1.53] a lysosomal hexosaminidase specifically catalyzing the cleavage of terminal, β-linked, nonreducing N-acetylgalactosamine residues from gangliosides or other glycosides.
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β-D-acetylglucosaminidase a lysosomal hexosaminidase now recognized as the same enzyme as β-N-acetylhexosaminidase (q.v.).
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β-a. an ω-amino acid, β-aminopropionic acid; it is not found in proteins but occurs both free and in several peptides, is a precursor of acetyl coenzyme A and several related compounds, and is an intermediate in the catabolism of uracil and cytosine.
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β-alanine transaminase 1. β-alanine–α-ketoglutarate transaminase.  2. β-alanine–pyruvate transaminase.
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β-alanine–α-ketoglutarate transaminase an enzyme activity that transfers the amino group from β-alanine to α-ketoglutarate, forming glutamate and malonate semialdehyde as a step in the metabolism of β-alanine. The enzyme can also act on γ-aminobutyrate and S-β-aminoisobutyrate; it has been listed as a secondary activity of the enzyme 4-aminobutyrate transaminase but may be a separate enzyme. Deficiency of this enzyme activity causes hyper-β-alaninemia.
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