| An acetyl group was attached to residue 22 to mimic the preceding peptide bond and the C-terminal carboxylate was protonated. |
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| This indicates extraordinary peptidase stability of the peptide bond in cyclic dipeptides. |
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| The cleavage of the peptide bond in DKPs by various peptidases was studied. |
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| The far-UV region CD spectrum reflects the circular dichroism of peptide bond. |
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| Trypsin cleaves the peptide bond on the C-ter side of the amino acids lysine and arginine. |
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| Cyanogen bromide, on the other hand, cuts the peptide bond on the C-ter side of methionine. |
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| The peptide bond is very stable, its spontaneous hydrolysis is almost nil, but it can be hydrolysed by chemical or enzymatic. |
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| Thermolysin cuts the peptide bond on the N-terminal side of hydrophobic amino acids. |
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| This partial double bond character of the peptide bond means that rotation around the C-N bond is not possible, and the CO and NH atoms will be in the same plane. |
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| As a result, studies of uncoded peptide bond formation are founded in using NCAs as substrates for mimicking prebiotic processes. |
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| Peptide bond formation is a condensation reaction leading to the polymerization of amino acids into peptides and proteins. |
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