PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
15294286-4	2004	Expression of the modified gene generated a functional F1Fo complex in host yeast cells lacking a functional copy of the endogenous ATP2 gene, as judged by growth of rescued cells on lactate medium.	Lactic Acid	183-190	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	132-136
27169884-2	2016	In this study, it is demonstrated by fluorescence and transmission electron microscopy that atp2.1pgs1Delta mutant mitochondria lacking anionic phospholipids contain fragmented and swollen mitochondria with a completely disorganized inner membrane.	Phospholipids	144-157	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	92-96
27169884-3	2016	In the second part of this study, it was shown that the temperature sensitivity of the atp2.1pgs1Delta mutant was not suppressed by the osmotic stabilizer glucitol but by glucosamine, a precursor of chitin synthesis.	Sorbitol	155-163	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	87-91
27169884-3	2016	In the second part of this study, it was shown that the temperature sensitivity of the atp2.1pgs1Delta mutant was not suppressed by the osmotic stabilizer glucitol but by glucosamine, a precursor of chitin synthesis.	Glucosamine	171-182	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	87-91
27169884-3	2016	In the second part of this study, it was shown that the temperature sensitivity of the atp2.1pgs1Delta mutant was not suppressed by the osmotic stabilizer glucitol but by glucosamine, a precursor of chitin synthesis.	Chitin	199-205	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	87-91
27169884-4	2016	The atp2.1pgs1Delta mutant was hypersensitive to Calcofluor White and caffeine, resistant to Zymolyase, but its sensitivity to caspofungin was the same as the strains with the standard PGS1 gene.	Caffeine	70-78	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	4-8
27169884-4	2016	The atp2.1pgs1Delta mutant was hypersensitive to Calcofluor White and caffeine, resistant to Zymolyase, but its sensitivity to caspofungin was the same as the strains with the standard PGS1 gene.	Caspofungin	127-138	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	4-8
27169884-6	2016	The glucan level in the cell wall of the atp2.1pgs1Delta mutant was reduced by 4-8 %, but the level of chitin was almost double that in the wild-type strain.	Glucans	4-10	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	41-45
22712517-6	2012	Survival studies after exposure to lethal H2O2 doses using yeast strains bearing a gene deletion corresponding to proteins associated to lipid and vesicle traffic demonstrated for the first time that down-regulation of Kes1p, Vps4p and Ynl010wp and up-regulation of Atp1 and Atp2 increases resistance to H2O2.	Hydrogen Peroxide	42-46	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	275-279
25035869-8	2014	Among the six genes, over-expression of PDB1, ILV5, or ATP2 partially recovered the salt stress sensitivity of bdf1Delta.	Salts	84-88	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	55-59
17465979-5	2007	Suppression depended on the presence of particular amino acid residues in Atp2p, and required adenosine triphosphate (ATP) binding and/or ATP hydrolysis activity of Pex6p.	Adenosine Triphosphate	94-116	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	74-79
17465979-5	2007	Suppression depended on the presence of particular amino acid residues in Atp2p, and required adenosine triphosphate (ATP) binding and/or ATP hydrolysis activity of Pex6p.	Adenosine Triphosphate	118-121	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	74-79
17465979-5	2007	Suppression depended on the presence of particular amino acid residues in Atp2p, and required adenosine triphosphate (ATP) binding and/or ATP hydrolysis activity of Pex6p.	Adenosine Triphosphate	138-141	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	74-79
16339725-6	2005	A spontaneous suppressor of this slow-growth phenotype was found to convert a conserved glycine to serine in the beta subunit of F(1)-ATPase (atp2-227).	Glycine	88-95	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	142-146
16339725-6	2005	A spontaneous suppressor of this slow-growth phenotype was found to convert a conserved glycine to serine in the beta subunit of F(1)-ATPase (atp2-227).	Serine	99-105	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	142-146
15776236-7	2005	A part of YJR119c, YJR120w, YJR122w (CAF17) and YJR123w (RP55), which were reported by the yeast genome project, are contained in the ATP2 repeated units; and the middle ATP2 of the three ATP2s, ATP2b, is located between the two repeated units.	atp2s	188-193	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	134-138
15776236-7	2005	A part of YJR119c, YJR120w, YJR122w (CAF17) and YJR123w (RP55), which were reported by the yeast genome project, are contained in the ATP2 repeated units; and the middle ATP2 of the three ATP2s, ATP2b, is located between the two repeated units.	atp2s	188-193	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	170-174
15776236-8	2005	Expression of all three copies of ATP2 (ATP2a, ATP2b, ATP2c) was confirmed because a single or double ATP2-disruptant could grow on glycerol, but a triple ATP2-disruptant could not.	Glycerol	132-140	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	34-38
15776236-8	2005	Expression of all three copies of ATP2 (ATP2a, ATP2b, ATP2c) was confirmed because a single or double ATP2-disruptant could grow on glycerol, but a triple ATP2-disruptant could not.	Glycerol	132-140	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	40-44
15776236-8	2005	Expression of all three copies of ATP2 (ATP2a, ATP2b, ATP2c) was confirmed because a single or double ATP2-disruptant could grow on glycerol, but a triple ATP2-disruptant could not.	Glycerol	132-140	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	40-44
15776236-9	2005	In addition, of the three copies of ATP1 and ATP2, even if only one copy of the ATP1 and ATP2 genes remained, the cells grew on glycerol.	Glycerol	128-136	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	45-49
15776236-9	2005	In addition, of the three copies of ATP1 and ATP2, even if only one copy of the ATP1 and ATP2 genes remained, the cells grew on glycerol.	Glycerol	128-136	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	89-93
10744740-8	2000	An unlinked suppressor gene, ASC1 (alpha-subunit complementing) of the atp1-2 mutation (Gly(291) --> Asp) restored the growth defect phenotype on glycerol, but did not suppress either atp1-1 or the deletion mutant Deltaatp1.	Glycerol	149-157	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	71-77
11746603-1	2001	Exposure of Saccharomyces cerevisiae to 0.9 mM sorbic acid at pH 4.5 resulted in the upregulation of 10 proteins; Hsp42, Atp2, Hsp26, Ssa1 or Ssa2, Ssb1 or Ssb2, Ssc1, Ssa4, Ach1, Zwf1 and Tdh1; and the downregulation of three proteins; Ade16, Adh3 and Eno2.	Sorbic Acid	47-58	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	121-125
10744740-8	2000	An unlinked suppressor gene, ASC1 (alpha-subunit complementing) of the atp1-2 mutation (Gly(291) --> Asp) restored the growth defect phenotype on glycerol, but did not suppress either atp1-1 or the deletion mutant Deltaatp1.	Glycine	88-91	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	71-77
10416023-3	1999	In this study the effect of 1 mM linolenic acid on levels of Q6 and Q6H2 is assessed in both wild-type and respiration-deficient (atp2 delta) strains.	alpha-Linolenic Acid	33-47	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	130-134
10744740-8	2000	An unlinked suppressor gene, ASC1 (alpha-subunit complementing) of the atp1-2 mutation (Gly(291) --> Asp) restored the growth defect phenotype on glycerol, but did not suppress either atp1-1 or the deletion mutant Deltaatp1.	Aspartic Acid	104-107	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	71-77
6330727-5	1984	Yeast cells carrying the ATP2-lacZ gene fusion on plasmid p beta Z1 are unable to grow on a nonfermentable carbon source.	Carbon	107-113	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	25-29
2866186-4	1985	Expression of an in-frame deletion in ATP2 between residues 28 and 34 to eliminate this single cysteine residue located near the processing site of the matrix protease does not prevent the in vivo delivery of the subunit to mitochondria or its assembly into a functional ATPase complex.	Cysteine	95-103	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	38-42
9495741-7	1998	A subset of these genes were found to be superinduced at the diauxic transition, and others were subject to cAMP repression (including ACH1, ADH2, ALD6, ATP2, GPD1, ICL1, and KGD2).	Cyclic AMP	108-112	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	153-157
6228552-5	1983	Transformation with ATP2 restored the growth rate of S. pombe mutant on glycerol as well as the mitochondrial ATPase and 32Pi-ATP exchange activities to approximately 20% of the parental strain.	Glycerol	72-80	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	20-24
6228552-5	1983	Transformation with ATP2 restored the growth rate of S. pombe mutant on glycerol as well as the mitochondrial ATPase and 32Pi-ATP exchange activities to approximately 20% of the parental strain.	32pi	121-125	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	20-24
29719209-8	2018	Expression of Atp2-T124 or T317 phosphomimetics also increased mitochondrial respiration and ATP levels and extended yeast lifespan.	Adenosine Triphosphate	93-96	F1F0 ATP synthase subunit beta	Saccharomyces cerevisiae S288C	14-18