Threonine (abbreviated as
Thr or
T) is an α-
amino acid with the
chemical formula HO
2CCH(NH
2)CH(OH)CH
3. Its
codons are ACU, ACA, ACC, and ACG. 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. In addition, threonine residues undergo
phosphorylation through the action of a threonine
kinase. In its phosphorylated form, it can be referred to as
phosphothreonine.
Stereoisomerism
With two
chiral centers, threonine can exist in four possible
stereoisomers with the following configurations: (2
S,3
R), (2
R,3
S), (2
S,3
S) und (2
R,3
R). However, the name
L-threonine is used for one single
enantiomer, (2
S,3
R)-2-amino-3-hydroxybutanoic acid. The second stereoisomer (2
S,3
S), which is rarely present in nature, is called
L-
allo-threonine. The two stereoisomers (2
R,3
S)- and (2
R,3
R)-2-amino-3-hydroxybutanoic acid are only of minor importance.
Biosynthesis
As an essential amino acid, threonine is not synthesized in humans, hence we must ingest threonine in the form of 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. Enzymes involved in a typical biosynthesis of threonine include:

Threonine biosynthesis
Metabolism
Threonine is metabolized in two ways:
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.