PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17020320-1	2006	[structure: see text] The coumarin antibiotics are not only potent inhibitors of DNA gyrase but also represent the most effective C-terminal inhibitors of 90 kDa heat shock proteins (Hsp90) reported thus far.	coumarin	26-34	DNA topoisomerase II alpha	Homo sapiens	81-91	
11743689-1	2002	DNA gyrase is the target of coumarin and cyclothialidine antibacterials, which bind to the B subunit of the enzyme (GyrB).	coumarin	28-36	DNA topoisomerase II alpha	Homo sapiens	0-10	
12044152-0	2002	DNA gyrase interaction with coumarin-based inhibitors: the role of the hydroxybenzoate isopentenyl moiety and the 5"-methyl group of the noviose.	coumarin	28-36	DNA topoisomerase II alpha	Homo sapiens	0-10	
8383523-0	1993	The 43-kilodalton N-terminal fragment of the DNA gyrase B protein hydrolyzes ATP and binds coumarin drugs.	coumarin	91-99	DNA topoisomerase II alpha	Homo sapiens	45-55	
8664301-0	1996	The interaction of coumarin antibiotics with fragments of DNA gyrase B protein.	coumarin	19-27	DNA topoisomerase II alpha	Homo sapiens	58-68	
8664301-1	1996	DNA gyrase is the target of the coumarin group of antibacterial agents.	coumarin	32-40	DNA topoisomerase II alpha	Homo sapiens	0-10	
8231802-0	1993	The interaction between coumarin drugs and DNA gyrase.	coumarin	24-32	DNA topoisomerase II alpha	Homo sapiens	43-53	
8231802-1	1993	The coumarin group of antibiotics have as their target the bacterial enzyme DNA gyrase.	coumarin	4-12	DNA topoisomerase II alpha	Homo sapiens	76-86