PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2381873-8	1990	A Schild plot revealed that EM-523 was a competitive inhibitor of motilin receptor binding in man and in rabbit.	EM 523	28-34	motilin	Homo sapiens	66-73
2381873-9	1990	We conclude that EM-523 is a potent motilin agonist.	EM 523	17-23	promotilin	Oryctolagus cuniculus	36-43
32066337-4	2021	The results showed two conditions which appear to be essential that peptides presented ACE inhibition capacity: i) to interact with Zn2+ coordinated residues, such as His383, His387, and Glu411, by short hydrogen bonds, for peptides with high inhibitory capacity in vitro, as ALNEINQFYQK (IACE = 80.7%), NAVPITPTLNR (IACE = 80.7%), and FALPQYLK (IACE = 79.0%); or interact by electrostatic and hydrophobic interactions with the same residues, for peptides with intermediate inhibition capacity in vitro, as HQGLPQEVLNENLLR (IACE = 49.2%), FFVAPFPEVFGK (IACE = 47.8%) and YLGYLEQLLR (IACE = 47.8%); ii) to interact with the S1 active site residues (Ala354, Glu384, and Tyr523) by hydrogen bonds.	EM 523	668-674	angiotensin I converting enzyme	Bos taurus	87-90
32043855-3	2020	In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature and layered hexagonal NCM at high temperature (HT-NCM).	EM 523	38-44	CWC22 spliceosome associated protein homolog	Homo sapiens	85-88
32043855-3	2020	In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature and layered hexagonal NCM at high temperature (HT-NCM).	EM 523	38-44	CWC22 spliceosome associated protein homolog	Homo sapiens	85-88
32043855-3	2020	In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature and layered hexagonal NCM at high temperature (HT-NCM).	EM 523	38-44	CWC22 spliceosome associated protein homolog	Homo sapiens	85-88
32043855-3	2020	In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature and layered hexagonal NCM at high temperature (HT-NCM).	EM 523	38-44	CWC22 spliceosome associated protein homolog	Homo sapiens	85-88
32043855-3	2020	In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature and layered hexagonal NCM at high temperature (HT-NCM).	EM 523	38-44	CWC22 spliceosome associated protein homolog	Homo sapiens	85-88
31841328-3	2020	Molecular docking predicted that RGM-(Hyp)-GF and the ACE residues of Glu384, His513 and Lys511 formed hydrogen-bonding interactions at distances of 2.57, 2.99 and 2.42+3.0 A. RGL-(Hyp)-GL formed hydrogen bonds with Lys511 and Tyr523 and generated hydrogen-bonding interactions with His387 and Glu411 in the zinc(II) complexation motif at distances of 2.74 and 3.03+1.93 A.	EM 523	227-233	angiotensin I converting enzyme	Bos taurus	54-57