PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
24333487-6	2014	Our findings reveal novel interactions of the BRPF1 bromodomain with multiple acetyllysine residues on the N-terminus of histones and show that it preferentially selects for H2AK5ac, H4K12ac, and H3K14ac.	N-epsilon-Acetyl-L-lysine	78-90	bromodomain and PHD finger containing 1	Homo sapiens	46-51
26341557-5	2015	Our findings establish a highly conserved acetyllysine reader function for the YEATS domain protein family and highlight the significance of this interaction for Taf14.	N-epsilon-Acetyl-L-lysine	42-54	TATA-binding protein-associated factor TAF14	Saccharomyces cerevisiae S288C	162-167
25152236-6	2014	These results suggest that the acetylation of PDHA1 provides another layer of enzymatic regulation, in addition to phosphorylation, involving a reversible acetyllysine, suggesting that the acetylome, as well as the kinome, links glycolysis to respiration.	N-epsilon-Acetyl-L-lysine	155-167	pyruvate dehydrogenase E1 subunit alpha 1	Homo sapiens	46-51
25703523-2	2015	Binding of the lead compound 11 to the bromodomain of BRD9 results in an unprecedented rearrangement of residues forming the acetyllysine recognition site, affecting plasticity of the protein in an induced-fit pocket.	N-epsilon-Acetyl-L-lysine	125-137	bromodomain containing 9	Homo sapiens	54-58
25417107-4	2014	Crystal structural studies revealed that AF9 YEATS adopts an eight-stranded immunoglobin fold and utilizes a serine-lined aromatic "sandwiching" cage for acetyllysine readout, representing a novel recognition mechanism that is distinct from that of known acetyllysine readers.	N-epsilon-Acetyl-L-lysine	154-166	MLLT3 super elongation complex subunit	Homo sapiens	41-44
25417107-4	2014	Crystal structural studies revealed that AF9 YEATS adopts an eight-stranded immunoglobin fold and utilizes a serine-lined aromatic "sandwiching" cage for acetyllysine readout, representing a novel recognition mechanism that is distinct from that of known acetyllysine readers.	N-epsilon-Acetyl-L-lysine	255-267	MLLT3 super elongation complex subunit	Homo sapiens	41-44
24333487-9	2014	Our results outline the molecular mechanism driving binding specificity of the BRPF1 bromodomain for discrete acetyllysine residues on the N-terminal histone tails.	N-epsilon-Acetyl-L-lysine	110-122	bromodomain and PHD finger containing 1	Homo sapiens	79-84
20726530-4	2010	To characterize this catalytic mechanism of acetyllysine deacetylation by Sir2, we employed a combined computational approach to carry out molecular modeling, molecular dynamics (MD) simulations, quantum mechanics/molecular mechanics (QM/MM) calculations on catalysis by both yeast Hst2 (homologue of SIR two 2) and bacterial Sir2TM (Sir2 homologue from Thermatoga maritima).	N-epsilon-Acetyl-L-lysine	44-56	histone deacetylase HST2	Saccharomyces cerevisiae S288C	282-286
24389023-1	2014	SIRT2 deacetylates specific acetyllysine residues in diverse proteins and is implicated in a variety of cellular processes.	N-epsilon-Acetyl-L-lysine	28-40	sirtuin 2	Homo sapiens	0-5
23426869-0	2013	Dissecting the roles of the N- and C-flanking residues of acetyllysine substrates for SIRT1 activity.	N-epsilon-Acetyl-L-lysine	58-70	sirtuin 1	Homo sapiens	86-91
23426869-1	2013	SIRT1 specificity: The multispecific SIRT1 enzyme catalyzes the deacetylation of acetyllysine residues within protein targets.	N-epsilon-Acetyl-L-lysine	81-93	sirtuin 1	Homo sapiens	0-5
23426869-1	2013	SIRT1 specificity: The multispecific SIRT1 enzyme catalyzes the deacetylation of acetyllysine residues within protein targets.	N-epsilon-Acetyl-L-lysine	81-93	sirtuin 1	Homo sapiens	37-42
20726530-4	2010	To characterize this catalytic mechanism of acetyllysine deacetylation by Sir2, we employed a combined computational approach to carry out molecular modeling, molecular dynamics (MD) simulations, quantum mechanics/molecular mechanics (QM/MM) calculations on catalysis by both yeast Hst2 (homologue of SIR two 2) and bacterial Sir2TM (Sir2 homologue from Thermatoga maritima).	N-epsilon-Acetyl-L-lysine	44-56	histone deacetylase HST2	Saccharomyces cerevisiae S288C	288-310
17189187-7	2006	Furthermore, the acetyllysine 120 (acetyl-K120) form of p53 specifically accumulates at proapoptotic target genes.	N-epsilon-Acetyl-L-lysine	17-29	tumor protein p53	Homo sapiens	56-59
17148447-9	2007	The two acetyllysine-binding pockets and a negatively charged secondary binding pocket, produced at the dimer interface in BRD2 BD1, may be the unique features that allow BRD2 BD1 to selectively bind to the acetylated H4 tail.	N-epsilon-Acetyl-L-lysine	8-20	bromodomain containing 2	Homo sapiens	123-127
17148447-9	2007	The two acetyllysine-binding pockets and a negatively charged secondary binding pocket, produced at the dimer interface in BRD2 BD1, may be the unique features that allow BRD2 BD1 to selectively bind to the acetylated H4 tail.	N-epsilon-Acetyl-L-lysine	8-20	defensin beta 1	Homo sapiens	128-131
17148447-9	2007	The two acetyllysine-binding pockets and a negatively charged secondary binding pocket, produced at the dimer interface in BRD2 BD1, may be the unique features that allow BRD2 BD1 to selectively bind to the acetylated H4 tail.	N-epsilon-Acetyl-L-lysine	8-20	bromodomain containing 2	Homo sapiens	171-175
17148447-9	2007	The two acetyllysine-binding pockets and a negatively charged secondary binding pocket, produced at the dimer interface in BRD2 BD1, may be the unique features that allow BRD2 BD1 to selectively bind to the acetylated H4 tail.	N-epsilon-Acetyl-L-lysine	8-20	defensin beta 1	Homo sapiens	176-179
20060508-3	2010	SIRT3 and SIRT5 are NAD(+)-dependent deacetylases that remove acetyl groups from acetyllysine-modified proteins and yield 2"-O-acetyl-ADP-ribose and nicotinamide.	N-epsilon-Acetyl-L-lysine	81-93	sirtuin 3	Homo sapiens	0-5
20060508-3	2010	SIRT3 and SIRT5 are NAD(+)-dependent deacetylases that remove acetyl groups from acetyllysine-modified proteins and yield 2"-O-acetyl-ADP-ribose and nicotinamide.	N-epsilon-Acetyl-L-lysine	81-93	sirtuin 5	Homo sapiens	10-15
19053282-9	2008	Finally, the structure of H143A HDAC8 complexed with an intact acetylated tetrapeptide substrate molecule confirms the importance of D101 for substrate binding and reveals how Y306 and the active site zinc ion together bind and activate the scissile amide linkage of acetyllysine.	N-epsilon-Acetyl-L-lysine	267-279	histone deacetylase 8	Homo sapiens	32-37
17274598-7	2007	Using NMR perturbation studies, we demonstrate the Brg1 bromodomain binds acetyllysine in the context of histone tails, with no comparable affinity for unacetylated peptides.	N-epsilon-Acetyl-L-lysine	74-86	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	Homo sapiens	51-55
16079223-6	2005	Since the bromodomain of YTA7 lacks a key tyrosine residue shown to be important for acetyllysine binding in other bromodomains, we confirmed that a GST-Yta7p bromodomain fusion was capable of binding to histones in vitro.	N-epsilon-Acetyl-L-lysine	85-97	Yta7p	Saccharomyces cerevisiae S288C	25-29
31755702-9	2019	Catalytic activity measurements with HDAC6 CD1 confirm the preference for peptide substrates containing C-terminal acetyllysine residues.	N-epsilon-Acetyl-L-lysine	115-127	histone deacetylase 6	Homo sapiens	37-42
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	lysine acetyltransferase 2A	Homo sapiens	29-33
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	lysine acetyltransferase 2B	Homo sapiens	35-39
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	TATA-box binding protein associated factor 1	Homo sapiens	41-45
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	CREB binding protein	Homo sapiens	50-53
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	tumor protein p53	Homo sapiens	120-123
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	MYB proto-oncogene, transcription factor	Homo sapiens	125-130
15382140-5	2004	For example, bromodomains of Gcn5, PCAF, TAF1 and CBP are able to recognize acetyllysine residues in histones, HIV Tat, p53, c-Myb or MyoD.	N-epsilon-Acetyl-L-lysine	76-88	myogenic differentiation 1	Homo sapiens	134-138
31755702-9	2019	Catalytic activity measurements with HDAC6 CD1 confirm the preference for peptide substrates containing C-terminal acetyllysine residues.	N-epsilon-Acetyl-L-lysine	115-127	CD1c molecule	Homo sapiens	43-46
31755702-10	2019	However, these measurements also show that CD1 exhibits weak activity for peptide substrates bearing certain small amino acids on the carboxyl side of the scissile acetyllysine residue.	N-epsilon-Acetyl-L-lysine	164-176	CD1c molecule	Homo sapiens	43-46
34853079-4	2022	We show that KAT6A is the initiator of a newly-described transcriptional control module in which KAT6A-catalyzed promoter H3K9ac is bound by the acetyllysine reader ENL, which in turn cooperates with a network of chromatin factors to induce transcriptional elongation.	N-epsilon-Acetyl-L-lysine	145-157	lysine acetyltransferase 6A	Homo sapiens	13-18
34853079-4	2022	We show that KAT6A is the initiator of a newly-described transcriptional control module in which KAT6A-catalyzed promoter H3K9ac is bound by the acetyllysine reader ENL, which in turn cooperates with a network of chromatin factors to induce transcriptional elongation.	N-epsilon-Acetyl-L-lysine	145-157	lysine acetyltransferase 6A	Homo sapiens	97-102
34853079-4	2022	We show that KAT6A is the initiator of a newly-described transcriptional control module in which KAT6A-catalyzed promoter H3K9ac is bound by the acetyllysine reader ENL, which in turn cooperates with a network of chromatin factors to induce transcriptional elongation.	N-epsilon-Acetyl-L-lysine	145-157	MLLT1 super elongation complex subunit	Homo sapiens	165-168
34502039-9	2021	Overall, we describe histone tail recognition by ATAD2 BRD and illustrate that one acetyllysine group is primarily engaged by the conserved asparagine (N1064), the "RVF" shelf residues, and the flexible ZA loop.	N-epsilon-Acetyl-L-lysine	83-95	ATPase family AAA domain containing 2	Homo sapiens	49-54
34448544-7	2021	Further, our MD simulation studies highlight the binding mode of acetyllysine (Kac) and the stability of bromodomain-histone peptide complexes.	N-epsilon-Acetyl-L-lysine	65-77	bromodomain and PHD finger containing 3	Homo sapiens	105-116
34644302-2	2021	TFP is known to be heavily modified by acetyllysine and succinyllysine post-translational modifications (PTMs), many of which are targeted for reversal by the mitochondrial sirtuin deacylases SIRT3 and SIRT5.	N-epsilon-Acetyl-L-lysine	39-51	tripartite motif-containing 39	Mus musculus	0-3
34644302-2	2021	TFP is known to be heavily modified by acetyllysine and succinyllysine post-translational modifications (PTMs), many of which are targeted for reversal by the mitochondrial sirtuin deacylases SIRT3 and SIRT5.	N-epsilon-Acetyl-L-lysine	39-51	sirtuin 3	Mus musculus	192-197
34644302-2	2021	TFP is known to be heavily modified by acetyllysine and succinyllysine post-translational modifications (PTMs), many of which are targeted for reversal by the mitochondrial sirtuin deacylases SIRT3 and SIRT5.	N-epsilon-Acetyl-L-lysine	39-51	sirtuin 5	Mus musculus	202-207
2441392-6	1987	Determination of the amino acid sequences of alpha 37-138 and alpha 25-50 showed that residue 40 in axonemal alpha-tubulin is epsilon N-acetyllysine.	N-epsilon-Acetyl-L-lysine	136-148	tubulin alpha-5 chain	Gallus gallus	109-122
34314149-2	2021	HDAC6 is an enzyme that deacetylates the acetyllysine residues of protein substrates, and the discovery of HDAC6 substrates, including tubulin, has revealed many roles of HDAC6 in cell biology.	N-epsilon-Acetyl-L-lysine	41-53	histone deacetylase 6	Homo sapiens	0-5
34314149-2	2021	HDAC6 is an enzyme that deacetylates the acetyllysine residues of protein substrates, and the discovery of HDAC6 substrates, including tubulin, has revealed many roles of HDAC6 in cell biology.	N-epsilon-Acetyl-L-lysine	41-53	histone deacetylase 6	Homo sapiens	171-176
29228881-0	2018	Unravelling novel congeners from acetyllysine mimicking ligand targeting a lysine acetyltransferase PCAF bromodomain.	N-epsilon-Acetyl-L-lysine	33-45	lysine acetyltransferase 2B	Homo sapiens	100-104
31358618-1	2019	The constitutively nuclear histone deacetylases (HDACs) 1, 2, and 3 erase acetyl marks on acetyllysine residues, alter the landscape of histone modifications, and modulate chromatin structure and dynamics and thereby crucially regulate gene transcription in higher eukaryotes.	N-epsilon-Acetyl-L-lysine	90-102	histone deacetylase 1	Homo sapiens	27-67
30496698-4	2019	The results show that DD1 is solely responsible for the deacetylation of substrates harboring the acetyllysine at their C terminus, whereas DD2 exclusively deacetylates peptides with an internal acetyllysine residue.	N-epsilon-Acetyl-L-lysine	98-110	aldo-keto reductase family 1 member C1	Homo sapiens	22-25
30496698-4	2019	The results show that DD1 is solely responsible for the deacetylation of substrates harboring the acetyllysine at their C terminus, whereas DD2 exclusively deacetylates peptides with an internal acetyllysine residue.	N-epsilon-Acetyl-L-lysine	195-207	aldo-keto reductase family 1 member C1	Homo sapiens	22-25
30496698-4	2019	The results show that DD1 is solely responsible for the deacetylation of substrates harboring the acetyllysine at their C terminus, whereas DD2 exclusively deacetylates peptides with an internal acetyllysine residue.	N-epsilon-Acetyl-L-lysine	195-207	aldo-keto reductase family 1 member C2	Homo sapiens	140-143
33749253-6	2021	Nevertheless, we show that also the MLLT1 mutants can be targeted by developed acetyllysine mimetic inhibitors with affinities similarly to wild-type.	N-epsilon-Acetyl-L-lysine	79-91	MLLT1 super elongation complex subunit	Homo sapiens	36-41
33084328-5	2020	Our analysis demonstrated that critical contacts required for bromodomain inhibitor coordination are conserved between the ATAD2/B bromodomains, with many residues playing a dual role in acetyllysine recognition.	N-epsilon-Acetyl-L-lysine	187-199	ATPase family AAA domain containing 2	Homo sapiens	123-128
32694708-5	2020	We further demonstrate that concurrent disruption of the acetyllysine binding function of BRD4 and the kinase activities of PI3K and CDK4/6 by the TP inhibitor improves efficacy in several cancer models.	N-epsilon-Acetyl-L-lysine	57-69	bromodomain containing 4	Homo sapiens	90-94
31677030-6	2020	Acetylation levels for acetyl-coA carboxylase (ACC1) were measured with the anti-acetyllysine antibody.	N-epsilon-Acetyl-L-lysine	81-93	acetyl-CoA carboxylase alpha	Homo sapiens	47-51
31127101-7	2019	Together, our findings reveal a previously uncharacterized acetyllysine reader and suggest that selective targeting of H4K16ac by MLL4 provides a direct functional link between MLL4, MOF and H4K16 acetylation.	N-epsilon-Acetyl-L-lysine	59-71	lysine methyltransferase 2B	Homo sapiens	130-134
31127101-7	2019	Together, our findings reveal a previously uncharacterized acetyllysine reader and suggest that selective targeting of H4K16ac by MLL4 provides a direct functional link between MLL4, MOF and H4K16 acetylation.	N-epsilon-Acetyl-L-lysine	59-71	lysine methyltransferase 2B	Homo sapiens	177-181
31127101-7	2019	Together, our findings reveal a previously uncharacterized acetyllysine reader and suggest that selective targeting of H4K16ac by MLL4 provides a direct functional link between MLL4, MOF and H4K16 acetylation.	N-epsilon-Acetyl-L-lysine	59-71	lysine acetyltransferase 8	Homo sapiens	183-186
30520161-3	2019	We solved the crystal structure of the ATAD2 bromodomain and found that it contains a disulfide bridge near the base of the acetyllysine binding pocket (Cys1057-Cys1079).	N-epsilon-Acetyl-L-lysine	124-136	ATPase family AAA domain containing 2	Homo sapiens	39-44
29228881-2	2018	In this study, a three featured E-Pharmacophore (ARR) was generated based on acetyllysine mimicking inhibitor of PCAF BRD which is available as co-crystal structure (PDB ID: 5FDZ).	N-epsilon-Acetyl-L-lysine	77-89	lysine acetyltransferase 2B	Homo sapiens	113-117
28516954-4	2017	The 2.85 A-resolution crystal structure of zebrafish HDAC10 complexed with a transition-state analogue inhibitor reveals that a glutamate gatekeeper and a sterically constricted active site confer specificity for N8-acetylspermidine hydrolysis and disfavour acetyllysine hydrolysis.	N-epsilon-Acetyl-L-lysine	258-270	histone deacetylase 10	Danio rerio	53-59
29595201-3	2018	Herein, an acetyllysine mimic has been exploited for detecting the conformational changes of acetylated p53-protein/DNA interactions by genetic code expansion and 19F NMR.	N-epsilon-Acetyl-L-lysine	11-23	tumor protein p53	Homo sapiens	104-107
29900004-6	2018	The crystal structure of the Gas41 YEATS domain in complex with the H3K27ac peptide revealed that, similar to the AF9 and ENL YEATS domains, Gas41 YEATS forms a serine-lined aromatic cage for acetyllysine recognition.	N-epsilon-Acetyl-L-lysine	192-204	YEATS domain containing 4	Mus musculus	29-34
29900004-6	2018	The crystal structure of the Gas41 YEATS domain in complex with the H3K27ac peptide revealed that, similar to the AF9 and ENL YEATS domains, Gas41 YEATS forms a serine-lined aromatic cage for acetyllysine recognition.	N-epsilon-Acetyl-L-lysine	192-204	myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3	Mus musculus	114-117
29900004-6	2018	The crystal structure of the Gas41 YEATS domain in complex with the H3K27ac peptide revealed that, similar to the AF9 and ENL YEATS domains, Gas41 YEATS forms a serine-lined aromatic cage for acetyllysine recognition.	N-epsilon-Acetyl-L-lysine	192-204	YEATS domain containing 4	Mus musculus	141-146
28369619-8	2017	BRD4, a well-characterized acetyllysine reader, has been shown to play a major role in regulating transcription of selected subsets of genes.	N-epsilon-Acetyl-L-lysine	27-39	bromodomain containing 4	Homo sapiens	0-4
26721445-1	2016	Histone deacetylase (HDAC) inhibitors are cancer treatments that inhibit the removal of the epigenetic modification acetyllysine on histones, resulting in altered gene expression.	N-epsilon-Acetyl-L-lysine	116-128	histone deacetylase 9	Homo sapiens	0-19
28137841-2	2017	Here, we report on the biological activity, the structural basis, and therapeutic effects of the family of multitargeted compounds that simultaneously disrupt functions of two critical MYC-mediating factors through inhibiting the acetyllysine binding of BRD4 and the kinase activity of PI3K.	N-epsilon-Acetyl-L-lysine	230-242	MYC proto-oncogene, bHLH transcription factor	Homo sapiens	185-188
28137841-2	2017	Here, we report on the biological activity, the structural basis, and therapeutic effects of the family of multitargeted compounds that simultaneously disrupt functions of two critical MYC-mediating factors through inhibiting the acetyllysine binding of BRD4 and the kinase activity of PI3K.	N-epsilon-Acetyl-L-lysine	230-242	bromodomain containing 4	Homo sapiens	254-258
27653680-3	2016	We show that mild chemical targeting of the acetyllysine-binding pockets of the BET bromodomains, the transcriptional bookmarking domains, robustly enhances reprogramming.	N-epsilon-Acetyl-L-lysine	44-56	delta/notch like EGF repeat containing	Homo sapiens	80-83
26820517-2	2016	Sirtuin 1 (SIRT1) and sirtuin 2 (SIRT2) are NAD(+)-dependent histone deacetylases that operate as post-translational regulators for the deacetylation of acetyllysine.	N-epsilon-Acetyl-L-lysine	153-165	sirtuin 1	Homo sapiens	0-9
26820517-2	2016	Sirtuin 1 (SIRT1) and sirtuin 2 (SIRT2) are NAD(+)-dependent histone deacetylases that operate as post-translational regulators for the deacetylation of acetyllysine.	N-epsilon-Acetyl-L-lysine	153-165	sirtuin 1	Homo sapiens	11-16
26820517-2	2016	Sirtuin 1 (SIRT1) and sirtuin 2 (SIRT2) are NAD(+)-dependent histone deacetylases that operate as post-translational regulators for the deacetylation of acetyllysine.	N-epsilon-Acetyl-L-lysine	153-165	sirtuin 2	Homo sapiens	22-31
26820517-2	2016	Sirtuin 1 (SIRT1) and sirtuin 2 (SIRT2) are NAD(+)-dependent histone deacetylases that operate as post-translational regulators for the deacetylation of acetyllysine.	N-epsilon-Acetyl-L-lysine	153-165	sirtuin 2	Homo sapiens	33-38
27454933-4	2016	The catalytic activity of CD2 from both species exhibited broad substrate specificity, whereas that of CD1 was highly specific for substrates bearing C-terminal acetyllysine residues.	N-epsilon-Acetyl-L-lysine	161-173	CD2 molecule	Homo sapiens	26-29
27454933-4	2016	The catalytic activity of CD2 from both species exhibited broad substrate specificity, whereas that of CD1 was highly specific for substrates bearing C-terminal acetyllysine residues.	N-epsilon-Acetyl-L-lysine	161-173	CD1c molecule	Homo sapiens	103-106
27167503-3	2016	Twenty crystal structures of BRPF1/ligand complexes show structural conservation in the acetyllysine binding site, common binding motifs, and unusual interactions (e.g., the replacement of a conserved water molecule).	N-epsilon-Acetyl-L-lysine	88-100	bromodomain and PHD finger containing 1	Homo sapiens	29-34
27105114-3	2016	Here we report that the AF9 YEATS domain displays selectively higher binding affinity for crotonyllysine over acetyllysine.	N-epsilon-Acetyl-L-lysine	110-122	MLLT3 super elongation complex subunit	Homo sapiens	24-27
26721445-1	2016	Histone deacetylase (HDAC) inhibitors are cancer treatments that inhibit the removal of the epigenetic modification acetyllysine on histones, resulting in altered gene expression.	N-epsilon-Acetyl-L-lysine	116-128	histone deacetylase 9	Homo sapiens	21-25
26934307-4	2016	We also summarize the latest findings underscoring a critical role of the acetyllysine binding function of AF9 and Taf14 in transcriptional regulation and DNA repair.	N-epsilon-Acetyl-L-lysine	74-86	MLLT3 super elongation complex subunit	Homo sapiens	107-110