PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
32023971-4	2020	We show that both 34S and 15N remobilizations from the rosette to the seeds are impaired in the atg5 mutants irrespective of salicylic acid accumulation and of sulphur nutrition.	(2e)-3-{5-[(2,4-Diaminopyrimidin-5-Yl)methyl]-2,3-Dimethoxyphenyl}-1-[(1s)-1-Phenylphthalazin-2(1h)-Yl]prop-2-En-1-One	18-21	autophagy protein Apg5 family	Arabidopsis thaliana	96-100
33528512-4	2021	We found that autophagy-defective Arabidopsis thaliana (atg2 and atg5) exhibited marked excess Zn-induced chlorosis and growth defects relative to wild-type.	Zinc	95-97	autophagy protein Apg5 family	Arabidopsis thaliana	65-69
33528512-6	2021	Interestingly, the excess Zn symptoms of atg5 were alleviated by supplementation of high levels of iron (Fe) to the media.	Zinc	26-28	autophagy protein Apg5 family	Arabidopsis thaliana	41-45
33528512-6	2021	Interestingly, the excess Zn symptoms of atg5 were alleviated by supplementation of high levels of iron (Fe) to the media.	Iron	99-103	autophagy protein Apg5 family	Arabidopsis thaliana	41-45
33528512-6	2021	Interestingly, the excess Zn symptoms of atg5 were alleviated by supplementation of high levels of iron (Fe) to the media.	Iron	105-107	autophagy protein Apg5 family	Arabidopsis thaliana	41-45
33528512-7	2021	Under excess Zn, in atg5, Fe starvation was especially severe in juvenile true leaves.	Zinc	13-15	autophagy protein Apg5 family	Arabidopsis thaliana	20-24
33528512-8	2021	Consistent with this, accumulation levels of Fe3+ near the shoot apical meristem was remarkably reduced in atg5.	ferric sulfate	45-49	autophagy protein Apg5 family	Arabidopsis thaliana	107-111
33051300-4	2020	Type-A ARR proteins were degraded by autophagy in an AUTOPHAGY-RELATED (ATG)5-dependent manner, and this degradation is promoted by phosphorylation on a conserved aspartate in the receiver domain of the type-A ARRs.	Aspartic Acid	163-172	autophagy protein Apg5 family	Arabidopsis thaliana	53-77
32023971-4	2020	We show that both 34S and 15N remobilizations from the rosette to the seeds are impaired in the atg5 mutants irrespective of salicylic acid accumulation and of sulphur nutrition.	15n	26-29	autophagy protein Apg5 family	Arabidopsis thaliana	96-100
31077612-6	2019	Significant accumulations of phospholipids and ceramides and changes in GIPCs (glycosyl-inositol-phosphoryl-ceramides) in atg5 mutants indicated large modifications in endomembrane-lipid and especially plasma membrane-lipid composition.	Phospholipids	29-42	autophagy protein Apg5 family	Arabidopsis thaliana	122-126
31077612-7	2019	Decreases in chloroplast proteins and galactolipids in atg5 under low nutrient conditions, indicated that chloroplasts were used as lipid reservoirs for beta-oxidation in atg5 mutants.	Galactolipids	38-51	autophagy protein Apg5 family	Arabidopsis thaliana	55-59
30395253-7	2019	In the atg5-1 mutant, which is completely defective in autophagy, the efficiency of Fe translocation from vegetative organs to seeds was severely decreased even when Fe was provided during seed formation.	Iron	84-86	autophagy protein Apg5 family	Arabidopsis thaliana	7-11
30395253-7	2019	In the atg5-1 mutant, which is completely defective in autophagy, the efficiency of Fe translocation from vegetative organs to seeds was severely decreased even when Fe was provided during seed formation.	Iron	166-168	autophagy protein Apg5 family	Arabidopsis thaliana	7-11
30395253-8	2019	Combining atg5-1 with the sid2 mutation that counteracts premature senescence associated with autophagy deficiency and using 57Fe pulse labeling, we propose a two-step mechanism in which Fe taken up de novo during seed formation is first accumulated in vegetative organs and subsequently remobilized to seeds.	Iron	127-129	autophagy protein Apg5 family	Arabidopsis thaliana	10-14
24510943-5	2014	Under mild salt stress, atg5 leaves retained high levels of Chls and all photosystem proteins and maintained a normal chloroplast structure.	Salts	11-15	autophagy protein Apg5 family	Arabidopsis thaliana	24-28
20574160-3	2010	In particular, two ubiquitin-like proteins, ATG8 and ATG12, which conjugate with phosphatidylethanolamine (PE) and ATG5, respectively, forming ATG8-PE and ATG12-ATG5 complexes, were shown to be essential in autophagosome formation.	phosphatidylethanolamine	81-105	autophagy protein Apg5 family	Arabidopsis thaliana	115-119
20574160-3	2010	In particular, two ubiquitin-like proteins, ATG8 and ATG12, which conjugate with phosphatidylethanolamine (PE) and ATG5, respectively, forming ATG8-PE and ATG12-ATG5 complexes, were shown to be essential in autophagosome formation.	phosphatidylethanolamine	81-105	autophagy protein Apg5 family	Arabidopsis thaliana	161-165
20574160-3	2010	In particular, two ubiquitin-like proteins, ATG8 and ATG12, which conjugate with phosphatidylethanolamine (PE) and ATG5, respectively, forming ATG8-PE and ATG12-ATG5 complexes, were shown to be essential in autophagosome formation.	phosphatidylethanolamine	107-109	autophagy protein Apg5 family	Arabidopsis thaliana	115-119
20574160-3	2010	In particular, two ubiquitin-like proteins, ATG8 and ATG12, which conjugate with phosphatidylethanolamine (PE) and ATG5, respectively, forming ATG8-PE and ATG12-ATG5 complexes, were shown to be essential in autophagosome formation.	phosphatidylethanolamine	107-109	autophagy protein Apg5 family	Arabidopsis thaliana	161-165
29281085-9	2018	Rubisco degradation assays and ABPP showed that the activities of proteasome and papain-like cysteine protease were increased in atg5 mutants.	Bropirimine	31-35	autophagy protein Apg5 family	Arabidopsis thaliana	129-133
29281085-10	2018	Whether these proteases play a back-up role in nutrient recycling and remobilization in atg mutants or act to promote cell death is discussed in relation to their accumulation patterns in the atg5 mutant compared with the salicylic acid-depleted atg5/sid2 double-mutant, and in low nitrate compared with high nitrate conditions.	Salicylic Acid	222-236	autophagy protein Apg5 family	Arabidopsis thaliana	246-250
29281085-10	2018	Whether these proteases play a back-up role in nutrient recycling and remobilization in atg mutants or act to promote cell death is discussed in relation to their accumulation patterns in the atg5 mutant compared with the salicylic acid-depleted atg5/sid2 double-mutant, and in low nitrate compared with high nitrate conditions.	Nitrates	282-289	autophagy protein Apg5 family	Arabidopsis thaliana	192-196
29281085-10	2018	Whether these proteases play a back-up role in nutrient recycling and remobilization in atg mutants or act to promote cell death is discussed in relation to their accumulation patterns in the atg5 mutant compared with the salicylic acid-depleted atg5/sid2 double-mutant, and in low nitrate compared with high nitrate conditions.	Nitrates	309-316	autophagy protein Apg5 family	Arabidopsis thaliana	192-196
18039664-4	2008	AtATG12b was conjugated to AtATG5 in a manner dependent on AtATG7, AtATG10, and ATP, whereas AtATG8a was conjugated to phosphatidylethanolamine (PE) in a manner dependent on AtATG7, AtATG3, and ATP.	atatg12b	0-8	autophagy protein Apg5 family	Arabidopsis thaliana	27-33
18039664-4	2008	AtATG12b was conjugated to AtATG5 in a manner dependent on AtATG7, AtATG10, and ATP, whereas AtATG8a was conjugated to phosphatidylethanolamine (PE) in a manner dependent on AtATG7, AtATG3, and ATP.	Adenosine Triphosphate	80-83	autophagy protein Apg5 family	Arabidopsis thaliana	27-33