PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
28804911-7	2017	RESULTS: We found that EtOH metabolism significantly increased the acetylation of SOD2 at 2 functionally relevant lysine sites, K68 and K122, resulting in a 40% decrease in enzyme activity while overall SOD2 abundance was unchanged.	Tetraethylammonium iodide	136-140	superoxide dismutase 2, mitochondrial	Mus musculus	82-86
33142150-6	2021	Indeed, using the acidic-pretreated wastewater as a fermentation medium decreased the lag phase, enhanced the growth of the strain K122 to reach a final biomass production of 20 x 108 cells/mL, increased culturable cell count to 262 x 106 cells/mL and improved oral toxicity against Ephestia kuehniella larvae by 68.4%.	Tetraethylammonium iodide	131-135	thrombopoietin	Mus musculus	190-192
33142150-6	2021	Indeed, using the acidic-pretreated wastewater as a fermentation medium decreased the lag phase, enhanced the growth of the strain K122 to reach a final biomass production of 20 x 108 cells/mL, increased culturable cell count to 262 x 106 cells/mL and improved oral toxicity against Ephestia kuehniella larvae by 68.4%.	Tetraethylammonium iodide	131-135	thrombopoietin	Mus musculus	245-247
28739857-3	2017	We found that acylation of K122 on SOD1, while not impacting SOD1 catalytic activity, suppressed the ability of SOD1 to inhibit mitochondrial metabolism at respiratory complex I.	Tetraethylammonium iodide	27-31	superoxide dismutase 1	Homo sapiens	35-39
28739857-4	2017	We found that deacylase depletion increased K122 acylation on SOD1, which blocked the suppression of respiration in a K122-dependent manner.	Tetraethylammonium iodide	44-48	superoxide dismutase 1	Homo sapiens	62-66
28739857-4	2017	We found that deacylase depletion increased K122 acylation on SOD1, which blocked the suppression of respiration in a K122-dependent manner.	Tetraethylammonium iodide	118-122	superoxide dismutase 1	Homo sapiens	62-66
23840712-13	2013	Furthermore, replacement of lysine K51, or K117+K122 in 14-3-3beta with glutamine, to mimic lysine acetylation, significantly reduced the interaction between 14-3-3beta and synaptopodin.	Tetraethylammonium iodide	48-52	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide	Mus musculus	56-66
23840712-13	2013	Furthermore, replacement of lysine K51, or K117+K122 in 14-3-3beta with glutamine, to mimic lysine acetylation, significantly reduced the interaction between 14-3-3beta and synaptopodin.	Tetraethylammonium iodide	48-52	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide	Mus musculus	158-168
22419549-5	2012	Acetylation at both positions K122 and K123 is associated with a decrease of the electrostatic potential at the p65/DNA interface, which is only partially counterbalanced by an increase of the local Na(+) concentration.	Tetraethylammonium iodide	30-34	RELA proto-oncogene, NF-kB subunit	Homo sapiens	112-115