ଲିଉସିନ୍,

leucine's Usage Examples:

In cobalamin (vitamin B12) deficient individuals, plasma concentrations of β-leucine.

in many tissues in the human body; however, most dietary leucine is metabolized within the liver, adipose tissue, and muscle tissue.

If a mutation in the ACAT1 gene reduces or eliminates the activity of this enzyme, the body is unable to process isoleucine and ketones properly.

such as the amino acid leucine for which he found a (nearly correct) molecular weight of 131 Da.

The ADAR modification causes an isoleucine/valine recoding event which lies in the ion-conducting pore of the potassium channel.

threonine, tryptophan, methionine, leucine, isoleucine, lysine, and histidine.

Organic compoundsMurchison contains common amino acids such as glycine, alanine, and glutamic acid as well as unusual ones such as isovaline and pseudoleucine.

1, leucine aminopeptidase, LAPs, leucyl peptidase, peptidase S, cytosol aminopeptidase, cathepsin III, L-leucine aminopeptidase.

Despite individual scores of 0, the combination of both in adequate amounts has a positive PDCAAS, with the limiting amino acids isoleucine, threonine, and methionine.

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine.

These tandem repeats commonly fold together to form a solenoid protein domain, termed leucine-rich.

leucine ("leu"), and the other containing methionine ("met").

variants by having both the E484K-mutation and a new F888L mutation (a substitution of phenylalanine (F) with leucine (L) in the S2 domain of the spike protein).

Synonyms:

essential amino acid,