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Homoserine (also called isothreonine) is an α- with the HO2CCH(NH2)CH2CH2OH. L-Homoserine is not one of the common amino acids encoded by DNA. It differs from the proteinogenic amino acid by insertion of an additional into the sidechain. Homoserine, or its , is the product of a cleavage of a by degradation of . Homoserine is an intermediate in the of three essential amino acids: , (an of homoserine), and .


Applications
Commercially, homoserine can serve as precursor to the synthesis of and 1,4-butanediol. Purified homoserine is used in enzyme structural studies. Also, homoserine has played important roles in studies to elucidate peptide synthesis and synthesis of glycopeptides. Bacterial cell lines can make copious amounts of this amino acid.


Biosynthesis
Its complete biosynthetic pathway includes , the tricarboxylic acid (TCA) or citric acid cycle (Krebs cycle), and the aspartate metabolic pathway. It forms by two reductions of via the intermediacy of aspartate semialdehyde.Berg, J. M.; Stryer, L. et al. (2002), Biochemistry. W.H. Freeman. Specifically, the enzyme homoserine dehydrogenase, in association with , catalyzes a reversible reaction that interconverts L-aspartate-4-semialdehyde to L-homoserine. Homoserine kinase and homoserine O-succinyltransferase convert homoserine to phosphohomoserine and O-succinyl homoserine, respectively. Homoserine is produced from via the intermediate aspartate-4-semialdehyde, which is produced from β-phosphoaspartate. By the action of homoserine dehydrogenases, the semialdehyde is converted to homoserine.


Other biochemical roles
L-Homoserine is substrate for homoserine kinase, yielding phosphohomoserine (homoserine-phosphate), which is converted by threonine synthase to L-threonine.

Homoserine is converted to O-succinyl homoserine by homoserine O-succinyltransferase. O-succinyl homoserine is a precursor to L-.

Homoserine inhibits aspartate kinase and glutamate dehydrogenase. Glutamate dehydrogenase reversibly converts to α-ketoglutarate and α-ketoglutarate coverts to through the citric cycle. Threonine acts as another allosteric inhibitor of aspartate kinase and homoserine dehydrogenase, but it is a competitive inhibitor of homoserine kinase.

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