PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8125130-2	1994	In these adducts C3b was radioactively labeled in the free thiol group generated during activation of the internal thioester of C3.	Sulfhydryl Compounds	59-64	complement C3	Homo sapiens	17-20	
1917974-4	1991	A 40-kDa dipeptide containing the covalent bond was identified by labeling the free thiol group (generated during activation of the internal thioester of C3b) with iodo[1-14C]acetamide and analyzed by amino acid sequencing.	Sulfhydryl Compounds	84-89	complement C3	Homo sapiens	154-157	
1947794-5	1991	Spontaneous dissociation of the complex could be partly avoided by HgCl2, a thiol reagent which inhibits the esterase-like activity of bound C3b.	Sulfhydryl Compounds	76-81	complement C3	Homo sapiens	141-144	
21620382-6	2011	However, when thiol was used as an acceptor, only a stereoselective addition at C-3 resulted, so as to form C-1, C-3 dithio-substituted 2-deoxypyranosides.	Sulfhydryl Compounds	14-19	complement C3	Homo sapiens	80-83	
6139373-10	1983	A tryptic peptide containing the 3H label was isolated following digestion of [3H]C3b on activated thiol-Sepharose.	Sulfhydryl Compounds	99-104	complement C3	Homo sapiens	82-85	
6853369-1	1983	Versatile methods for displacement of the C-3 sulfur side chain of carbapenems with other thiol groups.	Sulfhydryl Compounds	90-95	complement C3	Homo sapiens	42-45	
6934510-1	1980	Treatment of the third component of human complement (C3) with methylamine results in a loss of hemolytic function and the appearance of a thiol group.	Sulfhydryl Compounds	139-144	complement C3	Homo sapiens	42-56	
30259944-0	2019	Boronic acid-catalysed C-3 selective ring opening of 3,4-epoxy alcohols with thiophenols and thiols.	Sulfhydryl Compounds	93-99	complement C3	Homo sapiens	23-26	
30259944-1	2019	In this protocol we described a boronic acid-catalysed C-3 selective ring opening of 3,4-epoxy alcohols with thiophenols and thiols as nucleophiles.	Sulfhydryl Compounds	125-131	complement C3	Homo sapiens	55-58	
30465586-2	2018	This highly regioselective approach afforded C-3 functionalized products in excellent yield, and this methodology was found to be compatible with both aromatic and aliphatic thiols having electronic and steric divergence as well as diverse functional groups.	Sulfhydryl Compounds	174-180	complement C3	Homo sapiens	45-48	
21936007-5	2011	C3b possesses a thioester domain featuring an internal cycloglutamyl cysteine thioester; upon hydrolysis this yields a free thiol (Cys988) that was also fluorescently tagged.	Sulfhydryl Compounds	124-129	complement C3	Homo sapiens	0-3	
6544185-2	1984	This partially denatured C3 (C3i) was coupled to activated Thiol-Sepharose via its single SH group.	Sulfhydryl Compounds	59-64	complement C3	Homo sapiens	25-27	
6544185-2	1984	This partially denatured C3 (C3i) was coupled to activated Thiol-Sepharose via its single SH group.	Sulfhydryl Compounds	59-64	complement C3	Homo sapiens	29-32	
6544185-4	1984	C3i was also fixed to sheep red cells which had been supplied with activated thiol groups by treatment with N-succinimidyl-3-(2-pyridyldithio)-propionate.	Sulfhydryl Compounds	77-82	complement C3	Homo sapiens	0-3	
6903192-12	1980	Conversion of C3 to C3b exposes one sulfhydryl residue as does modification of C3 with methylamine.	Sulfhydryl Compounds	36-46	complement C3	Homo sapiens	14-16	
6903192-12	1980	Conversion of C3 to C3b exposes one sulfhydryl residue as does modification of C3 with methylamine.	Sulfhydryl Compounds	36-46	complement C3	Homo sapiens	20-23	
6903192-12	1980	Conversion of C3 to C3b exposes one sulfhydryl residue as does modification of C3 with methylamine.	Sulfhydryl Compounds	36-46	complement C3	Homo sapiens	20-22