THREONINE

'Threonine'
Systematic name	(2''S'',3''R'')-2-Amino- 3-hydroxybutanoic acid
Abbreviations	'Thr T'
Chemical formula	C4H9NO3
Molecular mass	119.12 g mol-1
Melting point	256 °C
Density	? g cm-3
Isoelectric point	5.60
p''K''a	2.20 8.96
PubChem	6288
CAS number	[72-19-5]
EINECS number	200-774-1
Chemical structure of Threonine Chemical structure of

'Threonine' is an α-amino acid with the chemical formula HO₂CCH(NH₂)CH(OH)CH₃. Its three letter code is thr, its one letter code is T, and its codons are ACU and ACA. This essential amino acid is classified as polar. Together with serine and tyrosine, threonine is one of three proteinogenic amino acids bearing an alcohol group.
The threonine residue is susceptible to numerous posttranslational modifications. The hydroxy side chain can undergo O-linked glycosylation. Additionally, threonine residues undergo phosphorylation through the action of a threonine kinase. In its phosphorylated form, it can be referred to as phosphothreonine.

Contents

Allo-threonine

Biosynthesis

Metabolism

Sources

References

External links

Allo-threonine

With two chiral centers, threonine can exist in four possible stereoisomers, or two possible diastereomers of L-threonine. However, the name L-threonine is used for one single enantiomer, (2''S'',3''R'')-2-amino-3-hydroxybutanoic acid. The second diastereomer (2''S'',3''S''), which is rarely present in nature, is called L-''allo''-threonine.

Biosynthesis

As an essential amino acid, threonine is not synthesized in humans, hence we must ingest threonine or, more commonly, threonine-containing proteins. In plants and microorganisms, threonine is synthesized from aspartic acid via α-aspartyl-semialdehyde and homoserine. Homoserine undergoes ''O''-phosphorylation; this phosphate ester undergoes hydrolysis concomitant with relocation of the OH group.^[1] Enzymes involved in a typical biosynthesis of threonine include:
# aspartokinase
# α-aspartate semialdehyde dehydrogenase
# homoserine dehydrogenase
# homoserine kinase
# threonine synthase

Metabolism

Threonine is metabolized in two ways:

★ It is converted to pyruvate via Threonine Dehydrogenase. An intermediate in this pathway can undergo thiolysis with CoA to produce Acetyl CoA and glycine.

★ In humans, it is converted to alpha-ketobutyrate in a less common pathway via the enzyme Serine dehydratase, and thereby enters the pathway leading to succinyl CoA.

Sources

Foods high in threonine include cottage cheese, poultry, fish, meat, lentils, and sesame seeds.
Racemic threonine can be prepared from crotonic acid by alpha-functionalization using mercury(II) acetate.^[2]

References

1. Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.
2.

External links

★ Threonine biosynthesis

★ Computational Chemistry Wiki

★ CID 205

★ CID 6288