Valine

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Valine
Chemical structure of Valine     Chemical structure of Valine
Systematic name (S)-2-amino-3-methyl-butanoic acid
Abbreviations Val
V
Chemical formula C5H11NO2
Molecular mass 117.15 g mol-1
Melting point 315 °C
Density 1.230 g cm-3
Isoelectric point 5.96
pKa 2.27
9.52
PubChem 1182
CAS number [72-18-4]
EINECS number 200-773-6
SMILES CC(C)C(N)C(=O)O
Disclaimer and references

Valine is one of the 20 proteinogenic amino acids. Nutritionally, valine is also an essential amino acid. It is named after the plant valerian.

In sickle-cell disease, it substitutes for the hydrophilic amino acid glutamic acid in hemoglobin: Because valine is hydrophobic, the hemoglobin does not fold correctly. Valine is uncharged overall, as its R group is neutral, and the charges from its amino and carboxylic acid groups balance out: a zwitterion.

Foods that are good sources of valine include cottage cheese, fish, poultry, peanuts, sesame seeds, and lentils.

In a 1994 report released by five top cigarette companies, valine is one of the 599 additives to cigarettes. Its use or purpose, however, is unknown, like most cigarette additives. [1]

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Major Families of Biochemicals
Peptides | Amino acids | Nucleic acids | Carbohydrates | Lipids | Terpenes | Carotenoids | Tetrapyrroles | Enzyme cofactors | Steroids | Flavonoids | Alkaloids | Polyketides | Glycosides
Analogues of nucleic acids: The 20 Common Amino Acids Analogues of nucleic 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)