PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35526097-3	2022	Mechanistically, Bifonazole binds ACE2 around residue K353, which consequently prevents association with RBD, thereby impacting entry and replication of Spike-pseudotyped viruses as well as native SARS-CoV-2 and its variants of concern (VOC).	Fluoroglycofen	54-58	angiotensin converting enzyme 2	Homo sapiens	34-38	
33501438-6	2021	Our recent analysis of the highly transmissible N501Y lineage B.1.1.7 mutation in SARS-CoV-2 also supports this model, identifying a less promiscuous Y501 interaction with ACE2 that favors more stable functional binding with the K353 site alone.	Fluoroglycofen	229-233	angiotensin converting enzyme 2	Homo sapiens	172-176	
35295301-13	2022	The docking results suggest that the key residues K353 and G496 may affect the binding energies and dynamics between the inferred anti-SARS-CoV-2 chemical agents and the junction of the spike protein-ACE2 interface.	Fluoroglycofen	50-54	angiotensin converting enzyme 2	Homo sapiens	200-204