PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19879767-0	2009	Spare interactions of highly potent [Arg(14),Lys(15)]nociceptin for cooperative induction of ORL1 receptor activation.	Lysine	45-48	opioid related nociceptin receptor 1	Homo sapiens	93-97	
19879767-1	2009	[Arg(14),Lys(15)]Nociceptin is a very potent for ORL1 receptor, showing a few times stronger binding activity and much more enhanced biological activity than endogenous nociceptin.	Lysine	9-12	opioid related nociceptin receptor 1	Homo sapiens	49-53	
19879767-4	2009	The mutant receptor Gln205Ala was found to be as active as wild-type ORL1 for both nociceptin and [Arg(14),Lys(15)]nociceptin.	Lysine	107-110	opioid related nociceptin receptor 1	Homo sapiens	69-73	
19577933-8	2009	The results indicate that specific interactions feasible for Arg/Lys and Trp in common must be there for aromatic residues in ORL1, thus forming a cation/pi interaction or pi/pi hydrophobic interaction.	Lysine	65-68	opioid related nociceptin receptor 1	Homo sapiens	126-130	
16814543-2	2006	Chimera peptides with long spacers (a Lys and five or eight Gly residues) showed synergistically improved affinity for both the mu-opioid receptor and ORL1 receptor, while the chimera peptides with short spacers (Lys residue only) showed decreased or similar affinity compared to the monomeric receptor ligands.	Lysine	38-41	opioid related nociceptin receptor 1	Homo sapiens	151-155