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<p>with its <a href="page.php?w=side_chain">side chain</a> bonded to its secondary <a href="page.php?w=amine">amine</a> nitrogen. Most <a href="page.php?w=amino_acid">amino acid</a>s have a strong energetic preference for the trans peptide bond conformation due to <a href="page.php?w=steric_hindrance">steric hindrance</a>, but proline's unusual structure stabilizes the cis form so that both isomers are populated under biologically relevant conditions. There are three major  classes of proteins with prolyl isomerase activity: <a href="page.php?w=cyclophilin">cyclophilin</a></p><p>
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