PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30300955-2	2018	The present approach relies on an asymmetric olefin cyclopropanation reaction catalyzed by an engineered myoglobin in the presence of ex situ generated diazoacetonitrile within a compartmentalized reaction system.	Alkenes	45-51	myoglobin	Homo sapiens	105-114	
25538035-0	2015	Highly diastereoselective and enantioselective olefin cyclopropanation using engineered myoglobin-based catalysts.	Alkenes	47-53	myoglobin	Homo sapiens	88-97	
32943150-4	2020	These strategies are effective for imparting these myoglobin-based cyclopropanation biocatalysts with altered and improved function, including tolerance to aerobic conditions and improved reactivity toward electrondeficient olefins.	Alkenes	224-231	myoglobin	Homo sapiens	51-60	
31133770-4	2019	In addition, substitution of the proximal histidine with an aspartate residue led to a myoglobin-based catalyst capable of promoting stereoselective olefin cyclopropanation under nonreducing conditions.	Alkenes	149-155	myoglobin	Homo sapiens	87-96