The chemical substance "H-Ala-Pro-Ala-OH," with the CAS number 61430-14-6, is a peptide composed of three amino acids: alanine (Ala), proline (Pro), and another alanine. This tripeptide features an N-terminal amino group (H-Ala) and a C-terminal carboxylic acid group (OH), indicating it is in its free acid form. The sequence of amino acids suggests that it may exhibit specific biological activities, potentially influencing protein synthesis or acting as a signaling molecule in various biochemical pathways. Peptides like H-Ala-Pro-Ala-OH can be synthesized through solid-phase peptide synthesis or other methods, and their properties, such as solubility, stability, and reactivity, can vary based on the surrounding environment, including pH and temperature. Additionally, the presence of proline may impart unique conformational characteristics, affecting the peptide's overall structure and function. Such peptides are often studied for their roles in biological systems and potential applications in pharmaceuticals or biotechnology.

H-Ala-Pro-Ala-OH

61430-14-6: The chemical substance "H-Ala-Pro-Ala-OH," with the CAS number 61430-14-6, is a peptide composed of three amino acids: alanine (Ala), proline (Pro), and another alanine. This tripeptide features an N-terminal amino group (H-Ala) and a C-terminal carboxylic acid group (OH), indicating it is in its free acid form. The sequence of amino acids suggests that it may exhibit specific biological activities, potentially influencing protein synthesis or acting as a signaling molecule in various biochemical pathways. Peptides like H-Ala-Pro-Ala-OH can be synthesized through solid-phase peptide synthesis or other methods, and their properties, such as solubility, stability, and reactivity, can vary based on the surrounding environment, including pH and temperature. Additionally, the presence of proline may impart unique conformational characteristics, affecting the peptide's overall structure and function. Such peptides are often studied for their roles in biological systems and potential applications in pharmaceuticals or biotechnology.

<p>H-Ala-Pro-Ala-OH is a fluorescent amino acid residue that can be used to study the structures of proteins. This amino acid is derived from histidine, and its fluorescence intensity increases when it binds to tryptophan residues near the active site of an enzyme. H-Ala-Pro-Ala-OH has been used for the structural analysis of mutant enzymes that have been engineered to show differences in substrate binding sites. This molecule also has a fluorogenic substrate, which can be used as a replacement for traditional substrates in order to highlight specific regions of a protein or enzyme. The quantum theory was used to calculate the x-ray diffraction data, which were then analyzed using software programs such as MOLMOL and XPLOR. These datasets were then used to create molecular models of H-Ala-Pro-Ala-OH.</p>

CAS 61430-14-6

H-Ala-Pro-Ala-OH

H-Ala-Pro-Ala-OH

Ref: 3D-FA108477