A peptidyl transferase enzyme would catalyze the condensation reaction of two amino acids to form a peptide bond. This enzymatic reaction is essential for protein synthesis in living organisms.
The chemical reaction that builds up complex proteins from amino acids is called a condensation reaction. In this process, amino acids are linked together by peptide bonds to form a polypeptide chain, which eventually folds into a functional protein.
An example of a condensation reaction is the formation of a peptide bond between two amino acids during protein synthesis. This reaction involves the loss of a water molecule and the joining of the amino acids to form a dipeptide.
The formation of a peptide linkage between amino acids is a condensation reaction, specifically a dehydration synthesis reaction. The other product in addition to the dipeptide is a molecule of water.
When amino acids are combined to build a protein, a condensation reaction occurs where the carboxyl group of one amino acid reacts with the amino group of another amino acid, forming a peptide bond. This links the amino acids together to form a chain, which then folds into a specific 3D structure determined by the sequence of amino acids.
The reaction that attaches fatty acid tails together is called esterification. Esterification involves a condensation reaction between a carboxylic acid group of one fatty acid and an alcohol group of another fatty acid to form an ester bond, resulting in the formation of a lipid molecule.
When the condensation reaction joins two amino acids a dipeptide and a water molecule form.
The chemical reaction that builds up complex proteins from amino acids is called a condensation reaction. In this process, amino acids are linked together by peptide bonds to form a polypeptide chain, which eventually folds into a functional protein.
An example of a condensation reaction is the formation of a peptide bond between two amino acids during protein synthesis. This reaction involves the loss of a water molecule and the joining of the amino acids to form a dipeptide.
The formation of a peptide linkage between amino acids is a condensation reaction, specifically a dehydration synthesis reaction. The other product in addition to the dipeptide is a molecule of water.
Polyester and polyamide fibers have ester units as their building blocks. Polyesters are formed by the condensation reaction of diols with dicarboxylic acids, while polyamides are formed by the condensation reaction of diamines with dicarboxylic acids.
When amino acids combine to form proteins or polypeptides a condensation reaction occurs. The carboxyl group of one molecule reacts with the amine group of the other molecule. One molecule of water is released and this results in C(O)NH, or a peptide bond. Condensation is the reaction: the opposite process is termed Hydrolysis.
The union of glycerol and fatty acids to form fat is an example of condensation reaction. In this reaction, water is released as a byproduct as glycerol and fatty acids combine to form a triglyceride molecule.
A peptide bond forms between adjacent amino acids during a condensation reaction. This bond is formed between the carboxyl group of one amino acid and the amino group of another amino acid, resulting in the release of a water molecule.
When amino acids are combined to build a protein, a condensation reaction occurs where the carboxyl group of one amino acid reacts with the amino group of another amino acid, forming a peptide bond. This links the amino acids together to form a chain, which then folds into a specific 3D structure determined by the sequence of amino acids.
Phillips reaction involves the condensation of ortho phenylenediamines with organic acids in presence of dilute mineral acids to furnish benzimidazoles. This is a reaction in which two amines are reacted with acids to get amides. in the first step one amine is reacted with acid to form an amide and then this amide is reacted with acid to form a second amide which is benzaimidazole. This benzaimidazole group will be having a basic structure of benzene in which one could find an imidazole group fused in it. This fused imidazole(5 membered ring structure) group will have two nitrogens in alternative positions.
it might be a protein.. since proteins are polymers of various amino acids..
The function of polar regions of amino acids on the active site of the enzyme is that it allows the reaction to take place more easily. The active site is the place where the actual chemical reaction takes place.