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DL-lysine

File:L-Lysin_-_L-Lysine.svg · Wikimedia Commons · See Wikimedia Commons

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Also known as lysine, 2,6-diaminohexanoic acid

thumb|Lysine ball and stick model spinning Lysine (symbol Lys or K) is an α-amino acid that is a precursor to many proteins. Lysine contains an α-amino group (which is in the protonated form when the lysine is dissolved in water at physiological pH), an α-carboxylic acid group (which is in the deprotonated form when the lysine is dissolved in water at physiological pH), and a side chain (which is partially protonated when the lysine is dissolved in water at physiological pH), and so it is classified as a basic, charged (in water at physiological pH), aliphatic amino acid. It is encoded by the

AI overview

# DL-lysine DL-lysine is a form of lysine, an amino acid that serves as a building block for proteins in living organisms. It matters because lysine is essential for protein synthesis and various biological functions, and the DL-form (containing both left and right-handed molecular versions) may be used in nutritional supplements, animal feed, and other applications where lysine supplementation is needed.

AI-generated from the Wikipedia summary — may contain errors.

Chemical data

Formula
C6H14N2O2
Molecular weight
146.19 g/mol
IUPAC name
2-amino-6-azaniumylhexanoate
SMILES
C(CC[NH3+])CC(C(=O)[O-])N
InChIKey
KDXKERNSBIXSRK-UHFFFAOYSA-N
XLogP
-2.4
Polar surface area
93.8 Ų
H-bond donors
2
H-bond acceptors
3
Formal charge
0

via PubChem

~21 min read

Encyclopedic overview

12 sections
Contents
  • Biosynthesis
  • DAP pathway
  • AAA pathway
  • Catabolism
  • Nutritional value
  • Dietary sources
  • Biological roles
  • Disputed roles
  • Roles in disease
  • Use of lysine in animal feed
  • In popular culture
  • References

thumb|Lysine ball and stick model spinning Lysine (symbol Lys or K) is an α-amino acid that is a precursor to many proteins. Lysine contains an α-amino group (which is in the protonated form when the lysine is dissolved in water at physiological pH), an α-carboxylic acid group (which is in the deprotonated form when the lysine is dissolved in water at physiological pH), and a side chain (which is partially protonated when the lysine is dissolved in water at physiological pH), and so it is classified as a basic, charged (in water at physiological pH), aliphatic amino acid. It is encoded by the codons AAA and AAG. Like almost all other amino acids, the α-carbon is chiral and lysine may refer to either enantiomer or a racemic mixture of both. For the purpose of this article, lysine will refer to the biologically active enantiomer L-lysine, where the α-carbon is in the S configuration.

The human body cannot synthesize lysine. It is essential in humans and must therefore be obtained from the diet. In organisms that synthesize lysine, two main biosynthetic pathways exist, the diaminopimelate and α-aminoadipate pathways, which employ distinct enzymes and substrates and are found in diverse organisms. Lysine catabolism occurs through one of several pathways, the most common of which is the saccharopine pathway.

Excerpted from Wikipedia’s “DL-lysine” article, available under the CC BY-SA 4.0 licence.

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