PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11456500-6	2001	Intramolecular deuterium isotope effects for the benzylic hydroxylation of o-xylene-alpha-(2)H(3), p-xylene-alpha-(2)H(3), 2-(2)H(3),6-dimethylnaphthalene, and 4-(2)H(3),4"-dimethylbiphenyl were determined for CYP4B1 and CYP2B1 to further map their active site dimensions.	Deuterium	15-24	cytochrome P450 4B1	Oryctolagus cuniculus	210-216	
11456500-9	2001	Isotope effects for the CYP4B1-mediated benzylic hydroxylation of o- and p-xylenes were fully expressed (k(H)/k(D) = 9.7 and 6.8, respectively), whereas deuterium isotope effects for the naphthyl and biphenyl derivatives were both substantially masked (k(H)/k(D) approximately equal to 1).	Deuterium	153-162	cytochrome P450 4B1	Oryctolagus cuniculus	24-30