PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
31841636-4	2020	The results, including a crystal structure of the clinically relevant VIM-2 metallo beta-lactamase in complex with the inhibitor, reveal the potential of boronate inhibitors without the canonical acylamino side chain for inhibition of a broader range of serine- and metallo- beta-lactamases compared to previous bicyclic boronates, including the metallo-beta-lactamase L1.	2,5-bis(acylamino)pyridine	196-205	vimentin 2, pseudogene	Homo sapiens	70-75