PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16916947-3	2006	This study first shows that glyceraldehyde can be used as GK-bypassing oxidative substrate and then examines whether the triose can metabolically activate beta-cells with low glucose responsiveness.	Glyceraldehyde	28-42	glucokinase	Homo sapiens	58-60	
16916947-8	2006	It is concluded that glucose low-responsive beta-cells can be metabolically activated by the GK-bypassing glyceraldehyde, increasing their acute biosynthetic response to glucose but not their maximal glucose-inducible biosynthetic capacity, which is considered subject to chronic regulation.	Glyceraldehyde	106-120	glucokinase	Homo sapiens	93-95	
8412503-1	1993	Glucokinase activity in pancreatic islets was dose-dependently inactivated by D-glyceraldehyde, whereas islet hexokinase activity was not altered.	Glyceraldehyde	78-94	glucokinase	Homo sapiens	0-11	
8412503-6	1993	Our study suggests that defective discrimination of glucose anomers by glyceraldehyde-treated islets may be caused by inactivation of glucokinase.	Glyceraldehyde	71-85	glucokinase	Homo sapiens	134-145