Phosphothreonine

Threonine

Names
IUPAC name Threonine
Other names 2-Amino-3-hydroxybutanoic acid
Identifiers
CAS Number	80-68-2 Y 72-19-5 (L-isomer) N
3D model (Jmol)	Interactive image
ChEBI	CHEBI:57926 Y
ChEMBL	ChEMBL291747 Y
ChemSpider	6051 Y
DrugBank	DB00156 Y
ECHA InfoCard	100.000.704
EC Number	201-300-6
IUPHAR/BPS	4785
PubChem	6288
UNII	2ZD004190S Y
InChI InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m1/s1 Y Key: AYFVYJQAPQTCCC-GBXIJSLDSA-N Y InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m1/s1 Key: AYFVYJQAPQTCCC-GBXIJSLDSA-N
SMILES C[C@H]([C@@H](C(=O)O)N)O
Properties
Chemical formula	C4H9NO3
Molar mass	119.12 g·mol−1
Solubility in water	(H2O, g/dl) 10.6(30°),14.1(52°),19.0(61°)
Acidity (pKa)	2.63 (carboxyl), 10.43 (amino)
Supplementary data page
Structure and properties	Refractive index (n), Dielectric constant (εr), etc.
Thermodynamic data	Phase behaviour solid–liquid–gas
Spectral data	UV, IR, NMR, MS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YN ?)
Infobox references

Threonine (abbreviated as Thr or T) encoded by the codons ACU, ACC, ACA, and ACG is an α-amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH+
3 form under biological conditions), an α-carboxylic acid group (which is in the deprotonated −COO⁻ form under biological conditions), and an alcohol containing side chain, classifying it as a polar, uncharged (at physiological pH) amino acid. It is essential in humans, meaning the body cannot synthesize it, and must be ingested in our diet. Threonine is synthesized from aspartate in bacteria such as E. coli.

Threonine sidechains are often hydrogen bonded; the commonest small motifs formed are ST turns, ST motifs (often at the beginning of alpha helices) and ST staples (usually at the middle of alpha helices).

The threonine residue is susceptible to numerous posttranslational modifications. The hydroxyl 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.

It is a precursor of glycine, and can be used as a prodrug to reliably elevate brain glycine levels.