However, not all peptide bonds are formed in this way.

This trio works together to break peptide bonds on polypeptides.

N-methylacetamide is often used as the simplest model in studies of the peptide bond.

A peptide bond can be broken by hydrolysis (the adding of water).

"The structural basis of ribosome activity in peptide bond synthesis".

Living organisms also employ enzymes to form peptide bonds; this process requires free energy.

This is accomplished through the cleavage of peptide bonds in the target proteins.

The amino acid residues are always joined by peptide bonds.

It showed, however, that had amino acids formed under these conditions, they could go on to form peptide bonds.

The planarity of the peptide bonds can be imposed as a further constraint.

At higher temperatures (37 to 60 C), peptide bonds assist in the formation of the reaction product.

Proteins are chains of amino acids joined together by peptide bonds.

The phosphoric acid would act as a catalyst for the formation of peptide bonds.

Collagenases are enzymes that break the peptide bonds in collagen.

The aspartyl residues are involved in the hydrolysis of the peptide bonds.

Strong mineral acids can readily hydrolyse the peptide bonds in a protein.

The fragmentation process primarily gives rise to cleavage products that break along peptide bonds.

Hofmeister argued for peptide bonds by process of elimination.

They are joined together with peptide bonds.

The bond joining the nitrogen and the carbon in the peptide bond is now broken.

This stored energy provides the majority of the energy needed for peptide bond formation during translation.

The amino acids in a polypeptide chain are linked by peptide bonds.

Note that water is required for normal peptide bond cleavage of the iminolactone intermediate.

Hydrolysis of proteins with broad specificity for peptide bonds.

It works by inhibiting peptide bond formation by the ribosome.