PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10677220-9	2000	The results also show that AP site analogues such as 1, 3-propanediol (Pr), tetrahydrofuran (F), or cyclopentanol (Cy) are not substrates but constitute good inhibitors of the wild-type yOgg1.	1,3-propanediol	53-69	8-oxoguanine glycosylase OGG1	Saccharomyces cerevisiae S288C	186-191