PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19681075-2	2009	Highlights of the sequence are a diastereoselective construction of the C3a-bromo-hexahydropyrrolo[2,3-b]indole nucleus, its Co(I)-induced C3a-C3a" dimerization, and the twofold or sequential amide-bond formation before cyclization to the diketopiperazine of the homo- or heterodimeric alkaloids, respectively.	Amides	192-197	complement C3	Homo sapiens	72-75	
24076198-5	2013	The conjugation of GA onto chitosan probably occurred between amine (C-2), hydroxyl groups (C-3 and C-6) of chitosan and carboxyl groups of GA, forming amide and ester linkages, respectively.	Amides	152-157	complement C3	Homo sapiens	92-95	
19443226-2	2009	In this study we synthesized new derivatives of 2-oxo-1,2-dihydropyridin-3-yl amides using a facile aminolysis reaction, in which different alkyl and aryl esters and amides are substituted at N-1 and C-3 of the heterocyclic ring.	Amides	78-84	complement C3	Homo sapiens	192-203	
19681075-2	2009	Highlights of the sequence are a diastereoselective construction of the C3a-bromo-hexahydropyrrolo[2,3-b]indole nucleus, its Co(I)-induced C3a-C3a" dimerization, and the twofold or sequential amide-bond formation before cyclization to the diketopiperazine of the homo- or heterodimeric alkaloids, respectively.	Amides	192-197	complement C3	Homo sapiens	139-142	
19681075-2	2009	Highlights of the sequence are a diastereoselective construction of the C3a-bromo-hexahydropyrrolo[2,3-b]indole nucleus, its Co(I)-induced C3a-C3a" dimerization, and the twofold or sequential amide-bond formation before cyclization to the diketopiperazine of the homo- or heterodimeric alkaloids, respectively.	Amides	192-197	complement C3	Homo sapiens	139-142	
21581454-3	2008	The amide subsituent at C-3 is coplanar with the pyridone ring, while the tert-butyl ester group is orthogonal to the pyridine ring.	Amides	4-9	complement C3	Homo sapiens	24-27	
11791932-2	2002	A covalent amide or ester linkage is thereby supposed to form between C3b and the surface itself.	Amides	11-16	complement C3	Homo sapiens	70-73	
17984207-7	2008	Using N. gonorrhoeae variants that predominantly expressed individual Opa proteins, we found that all Opa proteins tested (A, B, C, D, E, F, and I) bound C4b and C3b via amide and ester linkages, respectively.	Amides	170-175	complement C3	Homo sapiens	162-165	
11597463-4	2001	In the second type, both pharmacophore groups were connected to C-3 of the steroid through an alkenyl chain containing an amide moiety.	Amides	122-127	complement C3	Homo sapiens	64-67	
7883753-6	1994	C3 contains an intrachain thioester bond in the alpha chain (110 kDa) and upon activation to C3b, binds with membrane molecules by forming an ester or amide bond.	Amides	151-156	complement C3	Homo sapiens	93-96	
2404692-4	1990	When an activator of the alternative complement pathway is present, C3b becomes covalently attached to its surface via an ester or amide bond.	Amides	131-136	complement C3	Homo sapiens	68-71	
7316962-4	1981	Incubation of the C3b-antibody-antigen aggregates in buffers known to destroy ester linkages had little effect on the C3b-IgG complexes, which suggested that C3b and IgG might be linked by an amide bond.	Amides	192-197	complement C3	Homo sapiens	18-21	
26522948-3	2015	Subsequent elaboration with a variety of N-terminal amide capping groups produced agonists as potent as human C3a itself in stimulating Ca(2+) release from human macrophages.	Amides	52-57	complement C3	Homo sapiens	110-113	
25498022-2	2015	The methodology involves Corey-Link approach with suitably protected 3-oxo-D-gluco-furanose to introduce F/Cl as well as ester/amide functionalities at C-3 of glucose.	Amides	127-132	complement C3	Homo sapiens	152-155