PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
1731635-6	1992	After separation of C4H from D6aH on hydroxyapatite, the C4H was identified using anti-C4H antibody from Jerusalem artichoke (Helianthus tuberosus) (B. Gabriac et al., 1991, Arch.	Durapatite	37-51	trans-cinnamate 4-monooxygenase	Glycine max	57-60
21489652-4	2011	When applied in conjunction with piperonylic acid (PIP, an inhibitor of the cinnamate 4-hydroxylase, C4H), caffeic acid equalized the inhibitory effect of PIP, whereas the application of methylene dioxocinnamic acid (MDCA, an inhibitor of the 4-coumarate:CoA ligase, 4CL) plus caffeic acid decreased lignin production.	piperonylic acid	33-49	trans-cinnamate 4-monooxygenase	Glycine max	101-104
21489652-4	2011	When applied in conjunction with piperonylic acid (PIP, an inhibitor of the cinnamate 4-hydroxylase, C4H), caffeic acid equalized the inhibitory effect of PIP, whereas the application of methylene dioxocinnamic acid (MDCA, an inhibitor of the 4-coumarate:CoA ligase, 4CL) plus caffeic acid decreased lignin production.	piperonylic acid	51-54	trans-cinnamate 4-monooxygenase	Glycine max	101-104
21489652-4	2011	When applied in conjunction with piperonylic acid (PIP, an inhibitor of the cinnamate 4-hydroxylase, C4H), caffeic acid equalized the inhibitory effect of PIP, whereas the application of methylene dioxocinnamic acid (MDCA, an inhibitor of the 4-coumarate:CoA ligase, 4CL) plus caffeic acid decreased lignin production.	caffeic acid	107-119	trans-cinnamate 4-monooxygenase	Glycine max	101-104
18626717-9	2008	When applied jointly with piperonylic acid (an inhibitor of the cinnamate 4-hydroxylase, C4H), ferulic acid increased lignin content.	piperonylic acid	26-42	trans-cinnamate 4-monooxygenase	Glycine max	89-92
18626717-9	2008	When applied jointly with piperonylic acid (an inhibitor of the cinnamate 4-hydroxylase, C4H), ferulic acid increased lignin content.	ferulic acid	95-107	trans-cinnamate 4-monooxygenase	Glycine max	89-92
18626717-9	2008	When applied jointly with piperonylic acid (an inhibitor of the cinnamate 4-hydroxylase, C4H), ferulic acid increased lignin content.	Lignin	118-124	trans-cinnamate 4-monooxygenase	Glycine max	89-92
1731635-6	1992	After separation of C4H from D6aH on hydroxyapatite, the C4H was identified using anti-C4H antibody from Jerusalem artichoke (Helianthus tuberosus) (B. Gabriac et al., 1991, Arch.	Durapatite	37-51	trans-cinnamate 4-monooxygenase	Glycine max	57-60
1731635-10	1992	The two proteins show molecular weights of about 58,000 for C4H and about 55,000 for D6aH on sodium dodecyl sulfate-polyacrylamide gel electrophoresis.	Sodium Dodecyl Sulfate	93-115	trans-cinnamate 4-monooxygenase	Glycine max	60-63
1731635-10	1992	The two proteins show molecular weights of about 58,000 for C4H and about 55,000 for D6aH on sodium dodecyl sulfate-polyacrylamide gel electrophoresis.	polyacrylamide	116-130	trans-cinnamate 4-monooxygenase	Glycine max	60-63
26856401-0	2016	Twin anchors of the soybean isoflavonoid metabolon: evidence for tethering of the complex to the endoplasmic reticulum by IFS and C4H.	isoflavonoid	28-40	trans-cinnamate 4-monooxygenase	Glycine max	130-133
26856401-4	2016	Isoflavone synthase (IFS) and cinnamate 4-hydroxylase (C4H) have been shown to be tandem P450 enzymes that are anchored in the ER, interacting with soluble enzymes of the phenylpropanoid and isoflavonoid pathways (chalcone synthase, chalcone reductase and chalcone isomerase).	isoflavonoid	191-203	trans-cinnamate 4-monooxygenase	Glycine max	30-53
26856401-4	2016	Isoflavone synthase (IFS) and cinnamate 4-hydroxylase (C4H) have been shown to be tandem P450 enzymes that are anchored in the ER, interacting with soluble enzymes of the phenylpropanoid and isoflavonoid pathways (chalcone synthase, chalcone reductase and chalcone isomerase).	isoflavonoid	191-203	trans-cinnamate 4-monooxygenase	Glycine max	55-58
24710726-5	2014	In conclusion, enhanced UV-B radiation caused the increase in the flavonoid synthesis by promoting the activities of PAL, C4H, 4CL, and CHS in soybean seedlings.	Flavonoids	66-75	trans-cinnamate 4-monooxygenase	Glycine max	122-125
24710726-6	2014	The treatment of LaCl3 could change flavonoid synthesis in soybean seedlings under enhanced UV-B radiation by regulating the activities of PAL, C4H, 4CL, and CHS, which is an enzymological mechanism for the regulation of LaCl3 on flavonoid synthesis in plants under enhanced UV-B radiation.	Flavonoids	36-45	trans-cinnamate 4-monooxygenase	Glycine max	144-147
24710726-6	2014	The treatment of LaCl3 could change flavonoid synthesis in soybean seedlings under enhanced UV-B radiation by regulating the activities of PAL, C4H, 4CL, and CHS, which is an enzymological mechanism for the regulation of LaCl3 on flavonoid synthesis in plants under enhanced UV-B radiation.	Flavonoids	230-239	trans-cinnamate 4-monooxygenase	Glycine max	144-147
23922685-3	2013	The results revealed that exogenously applied cinnamic acid inhibited root growth and increased IAA oxidase and C4H activities.	cinnamic acid	46-59	trans-cinnamate 4-monooxygenase	Glycine max	112-115
23922685-5	2013	When applied alone or with cinnamic acid, piperonylic acid (PIP, a quasi-irreversible inhibitor of C4H) reduced C4H activity, lignin and the H, G, S monomer content compared to the cinnamic acid treatment.	piperonylic acid	42-58	trans-cinnamate 4-monooxygenase	Glycine max	99-102
23922685-5	2013	When applied alone or with cinnamic acid, piperonylic acid (PIP, a quasi-irreversible inhibitor of C4H) reduced C4H activity, lignin and the H, G, S monomer content compared to the cinnamic acid treatment.	piperonylic acid	42-58	trans-cinnamate 4-monooxygenase	Glycine max	112-115
23922685-5	2013	When applied alone or with cinnamic acid, piperonylic acid (PIP, a quasi-irreversible inhibitor of C4H) reduced C4H activity, lignin and the H, G, S monomer content compared to the cinnamic acid treatment.	piperonylic acid	60-63	trans-cinnamate 4-monooxygenase	Glycine max	99-102
23922685-5	2013	When applied alone or with cinnamic acid, piperonylic acid (PIP, a quasi-irreversible inhibitor of C4H) reduced C4H activity, lignin and the H, G, S monomer content compared to the cinnamic acid treatment.	piperonylic acid	60-63	trans-cinnamate 4-monooxygenase	Glycine max	112-115
23922685-5	2013	When applied alone or with cinnamic acid, piperonylic acid (PIP, a quasi-irreversible inhibitor of C4H) reduced C4H activity, lignin and the H, G, S monomer content compared to the cinnamic acid treatment.	Lignin	126-132	trans-cinnamate 4-monooxygenase	Glycine max	99-102
23922685-6	2013	Taken together, these results indicate that exogenously applied cinnamic acid can be channeled into the phenylpropanoid pathway via the C4H reaction, resulting in an increase in H lignin.	cinnamic acid	64-77	trans-cinnamate 4-monooxygenase	Glycine max	136-139
23922685-6	2013	Taken together, these results indicate that exogenously applied cinnamic acid can be channeled into the phenylpropanoid pathway via the C4H reaction, resulting in an increase in H lignin.	phenylpropanoid	104-119	trans-cinnamate 4-monooxygenase	Glycine max	136-139
23922685-6	2013	Taken together, these results indicate that exogenously applied cinnamic acid can be channeled into the phenylpropanoid pathway via the C4H reaction, resulting in an increase in H lignin.	h lignin	178-186	trans-cinnamate 4-monooxygenase	Glycine max	136-139