PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22568547-1	2012	We have studied glutathionylcobalamin (GS-Cbl) by optical spectroscopy and with density functional theory (DFT) and time-dependent DFT (TD-DFT) electronic structure methods of truncated geometric models.	glutathionylcobalamin	16-37	Cbl proto-oncogene	Homo sapiens	42-45	
22316335-1	2012	Synthetic Co(III) complexes containing N5 donor sets undergo glutathionylation to generate biomimetic species of glutathionylcobalamin (GSCbl), an important form of cobalamin (Cbl) found in nature.	glutathionylcobalamin	113-134	Cbl proto-oncogene	Homo sapiens	138-141	
16441149-7	2006	In the case of GSNO, the overall reaction is fast (k approximately 1.2 x 10(6) M(-1) s(-1)) and leads to formation of glutathionylcobalamin (Cbl(III)SG) and nitrosylcobalamin (Cbl(III)(NO-)) as the final cobalamin products.	glutathionylcobalamin	118-139	Cbl proto-oncogene	Homo sapiens	141-151	
16441149-7	2006	In the case of GSNO, the overall reaction is fast (k approximately 1.2 x 10(6) M(-1) s(-1)) and leads to formation of glutathionylcobalamin (Cbl(III)SG) and nitrosylcobalamin (Cbl(III)(NO-)) as the final cobalamin products.	glutathionylcobalamin	118-139	Cbl proto-oncogene	Homo sapiens	141-144	
11375680-1	2001	Glutathionylcobalamin (gamma-glutamylcysteinylglycinylcobalamin; gamma-GluCysGly-Cbl) is a natural product which functions as an intermediate in the biosynthesis of the active B(12) coenzymes adenosylcobalamin and methylcobalamin.	glutathionylcobalamin	0-21	Cbl proto-oncogene	Homo sapiens	81-84	
11375680-2	2001	Of interest to the present studies is glutathionylcobalamin"s unique stability in comparison to other thiolatocobalamins, notably the > or =6 x 10(4) fold less stable cysteinylcobalamin, Cys-Cbl.	glutathionylcobalamin	38-59	Cbl proto-oncogene	Homo sapiens	194-197