Amino acids are held together by peptide bonds. Peptide bonds are formed through a condensation reaction between the carboxyl group of one amino acid and the amino group of another amino acid, resulting in the formation of a covalent bond and the release of a water molecule.
A hexapeptide is a peptide composed of six amino acids linked together through peptide bonds. Since each peptide bond is formed between two amino acids, a hexapeptide would have 5 peptide bonds connecting the 6 amino acids.
Well... SORT of. Technically, the bases contain the NCO (amide) moiety that characterizes a peptide bond. However, they occur in heterocyclic rings, and it's stretching a point to call them "peptide bonds" since they're not linking two peptide residues. Also, they're in the cis-form, which is atypical of peptide bonds.
Well! Polypeptides are chain of amino-acids better known as proteins. Those amino-acids are join together by peptide bonds. Peptide bonds form when two amino-acids undego the process of condensation reaction, or dehydration synthesis where a carboxyl group of one amino-acid reacts with the amino group of another amino acid releasing water.
Peptide bonds are primarily found in proteins, which are polymers made up of amino acids. Peptide bonds form between the amino group of one amino acid and the carboxyl group of another amino acid during protein synthesis.
The bond formed between glycine and tyrosine would likely be a peptide bond, which occurs between the carboxyl group of one amino acid (glycine) and the amino group of another amino acid (tyrosine). Peptide bonds are formed through a condensation reaction, resulting in the formation of a dipeptide.
The condensation reaction of serine, glycine, and tyrosine structures would involve the removal of water molecules to form a peptide bond between the carboxyl group of one amino acid and the amino group of another. This process results in the formation of a tripeptide composed of serine, glycine, and tyrosine residues connected through peptide bonds.
peptide A.S.Apex :)
Pepsin is an enzyme that breaks down proteins into smaller peptides in the stomach by hydrolyzing peptide bonds. It functions best in an acidic environment and plays a key role in the initial digestion of proteins into smaller, more easily digestible peptides.
Proteins are formed by peptide bonds between amino acids.
PEPTIDE
Amino acids are held together by peptide bonds. Peptide bonds are formed through a condensation reaction between the carboxyl group of one amino acid and the amino group of another amino acid, resulting in the formation of a covalent bond and the release of a water molecule.
Proteins have their monomers, amino acids, joined together by peptide bonds.
A hexapeptide is a peptide composed of six amino acids linked together through peptide bonds. Since each peptide bond is formed between two amino acids, a hexapeptide would have 5 peptide bonds connecting the 6 amino acids.
Amino acids are connected together by peptide bonds. Peptide bonds form between the amino group of one amino acid and the carboxyl group of another amino acid, resulting in the formation of a peptide bond and a water molecule as a byproduct.
To write peptide bonds, it is important to make sure that you write them using the correct formulas. Amino acids are extremely important when it comes to peptide bonds, and writing them incorrectly can cause problems.
Well... SORT of. Technically, the bases contain the NCO (amide) moiety that characterizes a peptide bond. However, they occur in heterocyclic rings, and it's stretching a point to call them "peptide bonds" since they're not linking two peptide residues. Also, they're in the cis-form, which is atypical of peptide bonds.