PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8344293-5	1993	The amount of 5"-([(Z)-4-amino-2-butenyl]methylamino)-5"-deoxyadenosine, an irreversible inhibitor of AdoMetDC, necessary to inhibit cell growth was also five-times more in SAM-1 cells than in control cells.	MDL 73811	14-71	adenosylmethionine decarboxylase 1	Homo sapiens	102-110	
1301596-6	1992	Recently, powerful irreversible inhibitors of AdoMetDC have become available including 5"-([(Z)-4-amino-2-butenyl]methylamino)-5"-deoxyadenosine, an enzyme activated inhibitor and 5"-deoxy-5"-[(3-hydrazinopropyl)methylamino]adenosine which binds to the active site and forms a covalent bond with the pyruvate prosthetic group.	MDL 73811	87-144	adenosylmethionine decarboxylase 1	Homo sapiens	46-54	
1637820-0	1992	Purification of human S-adenosylmethionine decarboxylase expressed in Escherichia coli and use of this protein to investigate the mechanism of inhibition by the irreversible inhibitors, 5"-deoxy-5"-[(3-hydrazinopropyl)methylamino]adenosine and 5"-([(Z)-4-amino-2-butenyl]methylamino)-5"-deoxyadenosine.	MDL 73811	244-301	adenosylmethionine decarboxylase 1	Homo sapiens	22-56	
1637820-6	1992	Inactivation of AdoMetDC by 5"-([(Z)-4-amino-2-butenyl]methylamino]-5"-deoxyadenosine (AbeAdo) led to the appearance of a new peptide peak in the Lys-C protease digest.	MDL 73811	28-85	adenosylmethionine decarboxylase 1	Homo sapiens	16-24