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