PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12810727-2	2003	By use of site-directed mutagenesis and sequence comparisons, we have identified Cys-235, Asp-328, and His-362 as constituting a catalytic triad in human BACAT (hBACAT) and identifying BACAT as a member of the type I acyl-CoA thioesterase gene family.	Cysteine	81-84	bile acid-CoA:amino acid N-acyltransferase	Homo sapiens	154-159	
12810727-2	2003	By use of site-directed mutagenesis and sequence comparisons, we have identified Cys-235, Asp-328, and His-362 as constituting a catalytic triad in human BACAT (hBACAT) and identifying BACAT as a member of the type I acyl-CoA thioesterase gene family.	Cysteine	81-84	bile acid-CoA:amino acid N-acyltransferase	Homo sapiens	161-167	
12810727-2	2003	By use of site-directed mutagenesis and sequence comparisons, we have identified Cys-235, Asp-328, and His-362 as constituting a catalytic triad in human BACAT (hBACAT) and identifying BACAT as a member of the type I acyl-CoA thioesterase gene family.	Cysteine	81-84	bile acid-CoA:amino acid N-acyltransferase	Homo sapiens	162-167	
12239217-3	2002	In the present study, the function of the putative catalytic triad of hBAT was examined by chemical modification with the cysteine alkylating reagent N-ethylmaleimide (NEM) and by site-directed mutagenesis of the triad residues followed by enzymology studies of mutant and wild-type hBATs.	Cysteine	122-130	bile acid-CoA:amino acid N-acyltransferase	Homo sapiens	70-74	
17965457-4	2008	Because two of these amino acids (Cys and His) are members of the catalytic triad of human BAT, it was proposed that 4HNE would cause inactivation of this enzyme.	Cysteine	34-37	bile acid-CoA:amino acid N-acyltransferase	Homo sapiens	91-94