PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 17020832-6 1994 In MeOH and TFE, two beta-turn conformations associated with overlapping sequences and cis/trans isomerism at Pro-3 amide bond were seen to be in equilibrium. Amides 116-121 pyrroline-5-carboxylate reductase 1 Homo sapiens 110-115 12803495-6 2003 In order to investigate their inhibitory potency, the three amide surrogates were introduced in the Pro3-Val4 and Val4-Ala5 position of Z-Ala1-Ala2-Pro3-Val4-Ala5-Ala6-NHiPr, a substrate which is cleaved in the Val4-Ala5 position by human leukocyte elastase (HLE). Amides 60-65 pyrroline-5-carboxylate reductase 1 Homo sapiens 100-104 12803495-6 2003 In order to investigate their inhibitory potency, the three amide surrogates were introduced in the Pro3-Val4 and Val4-Ala5 position of Z-Ala1-Ala2-Pro3-Val4-Ala5-Ala6-NHiPr, a substrate which is cleaved in the Val4-Ala5 position by human leukocyte elastase (HLE). Amides 60-65 pyrroline-5-carboxylate reductase 1 Homo sapiens 148-152 28801573-6 2017 Solid-state NMR chemical shifts indicate the prolyl amide bond in the pi-clamp motif adopts a 1:1 ratio of the cis and trans conformation, while in the reaction product Pro3 was exclusively in trans. Amides 52-57 pyrroline-5-carboxylate reductase 1 Homo sapiens 169-173