The chemical substance known as "ala-pro-gly," with the CAS number 36301-96-9, is a tripeptide composed of three amino acids: alanine (Ala), proline (Pro), and glycine (Gly). This peptide is characterized by its specific sequence, which influences its structural and functional properties. Tripeptides like ala-pro-gly are typically soluble in water due to the presence of polar amino acids, and they can exhibit various biological activities, including roles in signaling and metabolism. The presence of proline, known for its unique cyclic structure, can impart rigidity to the peptide chain, affecting its conformation and interactions with other biomolecules. Additionally, ala-pro-gly may be involved in various physiological processes and could serve as a building block for larger peptides or proteins. Its stability and reactivity can be influenced by factors such as pH and temperature, making it of interest in both biochemical research and potential therapeutic applications.

ala-pro-gly

36301-96-9: The chemical substance known as "ala-pro-gly," with the CAS number 36301-96-9, is a tripeptide composed of three amino acids: alanine (Ala), proline (Pro), and glycine (Gly). This peptide is characterized by its specific sequence, which influences its structural and functional properties. Tripeptides like ala-pro-gly are typically soluble in water due to the presence of polar amino acids, and they can exhibit various biological activities, including roles in signaling and metabolism. The presence of proline, known for its unique cyclic structure, can impart rigidity to the peptide chain, affecting its conformation and interactions with other biomolecules. Additionally, ala-pro-gly may be involved in various physiological processes and could serve as a building block for larger peptides or proteins. Its stability and reactivity can be influenced by factors such as pH and temperature, making it of interest in both biochemical research and potential therapeutic applications.

<p>Glycine is a small, sweet-tasting amino acid that is used in the biosynthesis of proteins. It has three linkages: an amide linkage to proline, and an ester linkage to alanine. The l-glycine molecule exists as two possible tautomers, the enol and keto forms. The enol form predominates at physiological pH; however, at very low pH, the keto form predominates. Glycine also has a cyclic structure and can be classified as a tripeptide.</p>

CAS 36301-96-9

ala-pro-gly

H-Ala-Pro-Gly-OH

Ref: 3D-FA108479