Tyrosine
From Wikipedia, the free encyclopedia
| Tyrosine | |
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| Systematic name | (S)-2-Amino-3-(4-hydroxy- phenyl)-propanoic acid |
| Abbreviations | Tyr Y |
| Chemical formula | C9H11NO3 |
| Molecular mass | 181.19 g mol-1 |
| Melting point | 343 °C |
| Density | 1.456 g cm-3 |
| Isoelectric point | 5.66 |
| pKa | 2.24 9.04 10.10 |
| Molar extinction coefficient | 1420 M-1 cm-1 at 274.6 nm |
| CAS number | [60-18-4] |
| EINECS number | 200-460-4 |
| SMILES | Oc1ccc(CC(N)C(=O)O)cc1 |
Absoption and emission spectrum |
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| Disclaimer and references | |
Tyrosine (from the Greek tyros, meaning cheese, as it was first discovered in 1846 by German chemist Justus von Liebig in cheese[1][2]), 4-hydroxyphenylalanine, or 2-amino-3(4-hydroxyphenyl)-propanoic acid, is one of the 20 amino acids that are used by cells to synthesize proteins. It has a phenol side chain with a hydroxyl group. Upon the location of the hydroxyl group, there are three structural isomers of Tyr, namely para-Tyr (p-Tyr), meta-Tyr (m-Tyr) and ortho-Tyr (o-Tyr). Enzymatically, only the first isomer (p-Tyr) is produced from L-Phe by the Phe-hydroxylase enzyme. The other two isoforms, m-Tyr and o-Tyr can be produced as a consequence of free radical attack on Phe in states with increased oxidative stress.
Tyrosine is converted to DOPA by tyrosine hydroxylase, an enzyme.
It plays a key role in signal transduction, since it can be tagged with a phosphate group (phosphorylated) by protein kinases to alter the functionality and activity of certain enzymes. (In its phosphorylated state, it is sometimes referred to as phosphotyrosine.) Tyrosine is also precursor to the thyroid hormones thyroxine and triiodothyronine, the pigment melanin, and the biologically-active catecholamines dopamine, norepinephrine and epinephrine.
In Papaver somniferum, the opium poppy, it is used to produce morphine.
[edit] Biosynthesis
Tyrosine cannot be completely synthesized by animals, although it can be made by hydroxylation of phenylalanine if the latter is in abundant supply. It is produced by plants and most microorganisms from prephenate, an intermediate on the shikimate pathway.
Prephenate is oxidatively decarboxylated with retention of the hydroxyl group to give p-hydroxyphenylpyruvate. This is transaminated using glutamate as the nitrogen source to give tyrosine and α-ketoglutarate.
[edit] Tyrosine hydroxylase
Tyrosine hydroxylase (TH) is the rate-limiting enzyme involved in the synthesis of the catecholamines such as dopamine, norepinephrine and epinephrine.
[edit] Medical use
L-Tyrosine is sometimes recommended by practitioners as helpful for weight loss, clinical depression, Parkinson's Disease , and phenylketonuria; however, one study found that it had no impact on endurance exercise performance.[3]
[edit] See also
[edit] References
- GA Molnar et al. Kidney International 68:2281-2287, 2005 Abstract
- GA Molnar et al. Free Radical Research 39(12):1359-1366, 2005 Abstract
[edit] Notes
- ^ Tyrosine at infoplease.com
- ^ Tyrosine at etymonline.com
- ^ Parcell A.C., et al. Effects of L-tyrosine and carbohydrate ingestion on performance. Journal of Applied Physiology 2002 Nov; 93(5): 1590-97. Abstract
[edit] External links
- Phenylalanine and tyrosine biosynthesis
- Computational Chemistry Wiki
- Links to external chemical sources.
| The 20 Common Amino Acids | ||
|---|---|---|
| Alanine (dp) | Arginine (dp) | Asparagine (dp) | Aspartic acid (dp) | Cysteine (dp) | Glutamic acid (dp) | Glutamine (dp) | Glycine (dp) | Histidine (dp) | Isoleucine (dp) | Leucine (dp) | Lysine (dp) | Methionine (dp) | Phenylalanine (dp) | Proline (dp) | Serine (dp) | Threonine (dp) | Tryptophan (dp) | Tyrosine (dp) | Valine (dp) | ||
| ←Peptides | Major families of biochemicals | Nucleic acids→ |
