PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22057274-6	2012	In support of our structural data, we demonstrate that substitution of three N-terminal residues (Gly-19, His-25, and Phe-26) of FGF2 (a ligand that does not bind FGFR2b) for the corresponding residues of FGF1 (Phe-16, Asn-22, and Tyr-23) enables the FGF2 triple mutant to bind and activate FGFR2b.	Glycine	98-101	fibroblast growth factor 1	Homo sapiens	205-209	
1383494-5	1992	aFGF, basic fibroblast growth factor and several glycine-substituted point mutations of aFGF potently inhibited 0.1 nM [125I]aFGF binding.	Glycine	49-56	fibroblast growth factor 1	Homo sapiens	88-92	
1383494-5	1992	aFGF, basic fibroblast growth factor and several glycine-substituted point mutations of aFGF potently inhibited 0.1 nM [125I]aFGF binding.	Glycine	49-56	fibroblast growth factor 1	Homo sapiens	88-92