Methionine, glutamate dehydrogenase

Amino acid metabolism A artate aminotransferase Alanine aminotransferase Cysteine aminotransferase Tyrosine aminotransferase Leucine aminotransferase Alanine-ketoacid aminotransfoase Ornithine-ketoacid aminotransferase A artate carbamoyl transferase Methionine adenosyl transferase Glutamate decarboxylase Glutamate dehydrogenase Serine hydroxymethyltransferase Aminoacyl-sRNA synthetases... 

There are several points of attack on the protein molecule, and in glutamate dehydrogenase and RNase, exposure to UV in the presence of psoralen extensively modified histidine, methionine, tryptophan, phenylalanine and tyrosine residues by photo-oxidation. ... 

Dietary protein and methionine intakes affect glutamate dehydrogenase and alanine aminotransferase activities in the juvenile marine shrimp Penaeus monodon... 

Alanine appears to be formed primarily by alanine dehydrogenase in A. cylindrica, C. licheniformey P. boryanumy and A. nidulanSy because the inhibition of formation of glutamate and glutamine by methionine sulfoximine is not accompanied by a comparable inhibition in the formation of alanine (Table I). Moreover, alanine formation by these species was not reduced in the presence of aminooxy acetate, an inhibitor of amino transfer reactions (I3,J4). However, in A. variabilis alanine appears to be formed by a transamination reaction, because synthesis of [ N]alanine from was strongly inhibited in the presence of... 

So, the biosynthesis of methionine (Met, M), the first of the essential amino adds to be considered (Scheme 12.13), begins by the conversion of aspartate (Asp, D) to aspartate semialdehyde in the same way glutamate (Glu, E) was converted to glutamate semialdehyde (vide supra. Scheme 12.6). Phosphorylation on the terminal carboxylate of aspartate (Asp, D) by ATP in the presence of aspartate kinase (EC 2.7.2.4) and subsequent reduction of the aspart-4 yl phosphate by NADPH in the presence of aspartate semialdehyde dehydrogenase (EC 1.2.1.11) yields the aspartate semialdehyde. The aspartate semialdehyde is further reduced to homoserine (homoserine oxoreductase, EC 1.1.1.3) and the latter is succinylated by succinyl-CoA with the liberation of coenzyme A (CoA-SH) in the presence of homoserine O-succinyl-transferase (EC 2.3.1.46). Then, reaction with cysteine (Cys, C) in the presence of cystathionine y-synthase (EC 2.5.1.48) produces cystathionine and succinate. In the presence of the pyridoxal phosphate protein cystathionine P-lyase (EC 4.4.1.8), both ammonia and pyruvate are lost from cystathionine and homocysteine is produced. Finally, methylation on sulfur to generate methionine (Met, M) occurs by the donation of the methyl from 5-methyltetrahydrofolate in the presence of methonine synthase (EC 2.1.1.13). 

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