Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Automatic Gene Ontology annotation based on Rhea mapping
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Differences in the interactions of oncogenic adenovirus 12 early region 1A and nononcogenic adenovirus 2 early region 1A with the cellular coactivators p300 and CBP.
Synergistic signaling in fetal brain by STAT3-Smad1 complex bridged by p300.
Specificity of cyclin E-Cdk2, TFIIB, and E1A interactions with a common domain of the p300 coactivator.
Cooperation of Sp1 and p300 in the induction of the CDK inhibitor p21WAF1/CIP1 during NGF-mediated neuronal differentiation.
A novel cofactor for p300 that regulates the p53 response.
cAMP response element-binding protein-binding protein binds to human papillomavirus E2 protein and activates E2-dependent transcription.
The MSG1 non-DNA-binding transactivator binds to the p300/CBP coactivators, enhancing their functional link to the Smad transcription factors.
A novel transcriptional repression domain mediates p21(WAF1/CIP1) induction of p300 transactivation.
ATF-2 has intrinsic histone acetyltransferase activity which is modulated by phosphorylation.
Domains of Brn-2 that mediate homodimerization and interaction with general and melanocytic transcription factors.
A novel Rb- and p300-binding protein inhibits transactivation by MyoD.
A novel zinc finger protein TReP-132 interacts with CBP/p300 to regulate human CYP11A1 gene expression.
Regulation of human flap endonuclease-1 activity by acetylation through the transcriptional coactivator p300.
A TPR motif cofactor contributes to p300 activity in the p53 response.
Selective coactivation of estrogen-dependent transcription by CITED1 CBP/p300-binding protein.
Scaffold/matrix attachment region elements interact with a p300-scaffold attachment factor A complex and are bound by acetylated nucleosomes.
The HMG-I/Y-related protein p8 binds to p300 and Pax2 trans-activation domain-interacting protein to regulate the trans-activation activity of the Pax2A and Pax2B transcription factors on the glucagon gene promoter.
Dual roles of p300 in chromatin assembly and transcriptional activation in cooperation with nucleosome assembly protein 1 in vitro.
Multiprotein bridging factor-1 (MBF-1) is a cofactor for nuclear receptors that regulate lipid metabolism.
Cooperative activation of human papillomavirus type 8 gene expression by the E2 protein and the cellular coactivator p300.
ICAT inhibits beta-catenin binding to Tcf/Lef-family transcription factors and the general coactivator p300 using independent structural modules.
Regulation of E2A activities by histone acetyltransferases in B lymphocyte development.
Acetylation of RelA at discrete sites regulates distinct nuclear functions of NF-kappaB.
Synergism between p68 RNA helicase and the transcriptional coactivators CBP and p300.
Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2.
The activation domains, the proline-rich domain, and the C-terminal basic domain in p53 are necessary for acetylation of histones on the proximal p21 promoter and interaction with p300/CREB-binding protein.
The adenovirus E1A oncoprotein recruits the cellular TRRAP/GCN5 histone acetyltransferase complex.
p29ING4 and p28ING5 bind to p53 and p300, and enhance p53 activity.
P300/CBP acts as a coactivator to cartilage homeoprotein-1 (Cart1), paired-like homeoprotein, through acetylation of the conserved lysine residue adjacent to the homeodomain.
Homologous sequences in adenovirus E1A and human papillomavirus E7 proteins mediate interaction with the same set of cellular proteins.
Histone acetyltransferase-dependent chromatin remodeling and the vascular clock.
Dendrite development regulated by CREST, a calcium-regulated transcriptional activator.
Orphan nuclear receptor small heterodimer partner, a novel corepressor for a basic helix-loop-helix transcription factor BETA2/neuroD.
Structural mechanism of the bromodomain of the coactivator CBP in p53 transcriptional activation.
Positive and negative modulation of the transcriptional activity of the ETS factor ESE-1 through interaction with p300, CREB-binding protein, and Ku 70/86.
Small molecule blockade of transcriptional coactivation of the hypoxia-inducible factor pathway.
Hepatitis C virus core protein regulates p300/CBP co-activation function. Possible role in the regulation of NF-AT1 transcriptional activity.
A new effector pathway links ATM kinase with the DNA damage response.
Interferon regulatory factor 1 binding to p300 stimulates DNA-dependent acetylation of p53.
p53 Stabilization and accumulation induced by human vaccinia-related kinase 1.
The Smad3 linker region contains a transcriptional activation domain.
SIRT1 deacetylation and repression of p300 involves lysine residues 1020/1024 within the cell cycle regulatory domain 1.
Stat3 dimerization regulated by reversible acetylation of a single lysine residue.
PARP-10, a novel Myc-interacting protein with poly(ADP-ribose) polymerase activity, inhibits transformation.
Cited1 is a bifunctional transcriptional cofactor that regulates early nephronic patterning.
The coactivator p300 directly acetylates the forkhead transcription factor Foxo1 and stimulates Foxo1-induced transcription.
STAT3 nuclear import is independent of tyrosine phosphorylation and mediated by importin-alpha3.
NF-kappaB RelA phosphorylation regulates RelA acetylation.
p300 modulates ATF4 stability and transcriptional activity independently of its acetyltransferase domain.
The conserved Leu-724 residue is required for both serine phosphorylation and co-activator recruitment for Stat1-mediated transcription activation in response to interferon-gamma.
STAT3 NH2-terminal acetylation is activated by the hepatic acute-phase response and required for IL-6 induction of angiotensinogen.
A nuclear function of beta-arrestin1 in GPCR signaling: regulation of histone acetylation and gene transcription.
Acetylation and alternative splicing regulate ZNF76-mediated transcription.
Nuclear Rho kinase, ROCK2, targets p300 acetyltransferase.
Targeting of p300/CREB binding protein coactivators by simian virus 40 is mediated through p53.
Foxp3 represses retroviral transcription by targeting both NF-kappaB and CREB pathways.
The SWI/SNF chromatin-remodeling complex is a cofactor for Tat transactivation of the HIV promoter.
Bovine herpesvirus 1 immediate-early protein (bICP0) interacts with the histone acetyltransferase p300, which stimulates productive infection and gC promoter activity.
The transcriptional activity of CITED1 is regulated by phosphorylation in a cell cycle-dependent manner.
Roles of HIPK1 and HIPK2 in AML1- and p300-dependent transcription, hematopoiesis and blood vessel formation.
Interaction of GATA-3/T-bet transcription factors regulates expression of sialyl Lewis X homing receptors on Th1/Th2 lymphocytes.
Functional architecture of atrophins.
Lysine propionylation and butyrylation are novel post-translational modifications in histones.
Modulation of p300 binding by posttranslational modifications of the C-terminal activation domain of hypoxia-inducible factor-1alpha.
HLA-B-associated transcript 3 (Bat3)/Scythe is essential for p300-mediated acetylation of p53.
Four domains of p300 each bind tightly to a sequence spanning both transactivation subdomains of p53.
Cooperative interactions between CBP and TORC2 confer selectivity to CREB target gene expression.
MED25 is distinct from TRAP220/MED1 in cooperating with CBP for retinoid receptor activation.
Orphan receptor TR3 attenuates the p300-induced acetylation of retinoid X receptor-alpha.
Critical and functional regulation of CHOP (C/EBP homologous protein) through the N-terminal portion.
The prolyl isomerase Pin1 orchestrates p53 acetylation and dissociation from the apoptosis inhibitor iASPP.
Lyl1 interacts with CREB1 and alters expression of CREB1 target genes.
PTEN regulates p300-dependent hypoxia-inducible factor 1 transcriptional activity through Forkhead transcription factor 3a (FOXO3a).
Structure of tumor suppressor p53 and its intrinsically disordered N-terminal transactivation domain.
A transcription cofactor required for the heat-shock response.
Acetylation is indispensable for p53 activation.
Prohibitin and the SWI/SNF ATPase subunit BRG1 are required for effective androgen antagonist-mediated transcriptional repression of androgen receptor-regulated genes.
Induced ncRNAs allosterically modify RNA-binding proteins in cis to inhibit transcription.
NUPR1 interacts with p53, transcriptionally regulates p21 and rescues breast epithelial cells from doxorubicin-induced genotoxic stress.
Acetylation of Sirt2 by p300 attenuates its deacetylase activity.
The STAT3 NH2-terminal domain stabilizes enhanceosome assembly by interacting with the p300 bromodomain.
Hyaluronan-mediated CD44 interaction with p300 and SIRT1 regulates beta-catenin signaling and NFkappaB-specific transcription activity leading to MDR1 and Bcl-xL gene expression and chemoresistance in breast tumor cells.
Tcl1 functions as a transcriptional regulator and is directly involved in the pathogenesis of CLL.
Transcriptional activation of hypoxia-inducible factor-1alpha by HDAC4 and HDAC5 involves differential recruitment of p300 and FIH-1.
Structural basis for p300 Taz2-p53 TAD1 binding and modulation by phosphorylation.
Molecular basis of the interactions between the p73 N terminus and p300: effects on transactivation and modulation by phosphorylation.
Induction of SOX4 by DNA damage is critical for p53 stabilization and function.
Crosstalk between sumoylation and acetylation regulates p53-dependent chromatin transcription and DNA binding.
SENP3 is responsible for HIF-1 transactivation under mild oxidative stress via p300 de-SUMOylation.
Phosphorylation and acetylation of histone H3 and autoregulation by early growth response 1 mediate interleukin 1beta induction of early growth response 1 transcription.
Acetylation of Dna2 endonuclease/helicase and flap endonuclease 1 by p300 promotes DNA stability by creating long flap intermediates.
Vitamin D stimulates apoptosis in gastric cancer cells in synergy with trichostatin A /sodium butyrate-induced and 5-aza-2'-deoxycytidine-induced PTEN upregulation.
BRD7 is a candidate tumour suppressor gene required for p53 function.
Dual roles for MEF2A and MEF2D during human macrophage terminal differentiation and c-Jun expression.
RKTG inhibits angiogenesis by suppressing MAPK-mediated autocrine VEGF signaling and is downregulated in clear-cell renal cell carcinoma.
Siah2-dependent concerted activity of HIF and FoxA2 regulates formation of neuroendocrine phenotype and neuroendocrine prostate tumors.
SIRT1 is regulated by a PPAR{γ}-SIRT1 negative feedback loop associated with senescence.
A multiprotein complex necessary for both transcription and DNA replication at the β-globin locus.
Human AP endonuclease (APE1/Ref-1) and its acetylation regulate YB-1-p300 recruitment and RNA polymerase II loading in the drug-induced activation of multidrug resistance gene MDR1.
Acetylation of Rb by PCAF is required for nuclear localization and keratinocyte differentiation.
HDAC3 is negatively regulated by the nuclear protein DBC1.
Salt-inducible kinase 2 links transcriptional coactivator p300 phosphorylation to the prevention of ChREBP-dependent hepatic steatosis in mice.
Acetyltransferase p300 regulates NBS1-mediated DNA damage response.
Distinct roles of GCN5/PCAF-mediated H3K9ac and CBP/p300-mediated H3K18/27ac in nuclear receptor transactivation.
Novel nucleolar pathway connecting intracellular energy status with p53 activation.
The ASPP proteins complex and cooperate with p300 to modulate the transcriptional activity of p53.
Toward an understanding of the protein interaction network of the human liver.
Multiple site acetylation of Rictor stimulates mammalian target of rapamycin complex 2 (mTORC2)-dependent phosphorylation of Akt protein.
Acetylation-dependent regulation of Skp2 function.
Structural features of human histone acetyltransferase p300 and its complex with p53.
Human ALKBH4 interacts with proteins associated with transcription.
Regulation of the cyclin-dependent kinase inhibitor 1A gene (CDKN1A) by the repressor BOZF1 through inhibition of p53 acetylation and transcription factor Sp1 binding.
Regulation of transcription through acetylation of H3K122 on the lateral surface of the histone octamer.
The corepressor activity of Alien is controlled by CREB-binding protein/p300.
Interlaboratory reproducibility of large-scale human protein-complex analysis by standardized AP-MS.
Signal transducer and activator of transcription 6 directly regulates human ORMDL3 expression.
HIF1A employs CDK8-mediator to stimulate RNAPII elongation in response to hypoxia.
Role of p300 in regulating neuronal nitric oxide synthase gene expression through nuclear factor-κB-mediated way in neuronal cells.
SET1 and p300 act synergistically, through coupled histone modifications, in transcriptional activation by p53.
Structure of the p300 catalytic core and implications for chromatin targeting and HAT regulation.
Acetylation of the KXGS motifs in tau is a critical determinant in modulation of tau aggregation and clearance.
Kruppel-like factor 15 is critical for vascular inflammation.
Mitogenic and oncogenic stimulation of K433 acetylation promotes PKM2 protein kinase activity and nuclear localization.
Runx3 inactivation is a crucial early event in the development of lung adenocarcinoma.
Differential regulation of estrogen receptor α expression in breast cancer cells by metastasis-associated protein 1.
EAF2 suppresses hypoxia-induced factor 1α transcriptional activity by disrupting its interaction with coactivator CBP/p300.
Histone acetyltransferase-deficient p300 mutants in diffuse large B cell lymphoma have altered transcriptional regulatory activities and are required for optimal cell growth.
BAG6/BAT3 modulates autophagy by affecting EP300/p300 intracellular localization.
CBP and p300 acetylate PCNA to link its degradation with nucleotide excision repair synthesis.
Modification of ASC1 by UFM1 is crucial for ERα transactivation and breast cancer development.
Two ZNF509 (ZBTB49) isoforms induce cell-cycle arrest by activating transcription of p21/CDKN1A and RB upon exposure to genotoxic stress.
Acetylation of snail modulates the cytokinome of cancer cells to enhance the recruitment of macrophages.
Pokemon (FBI-1) interacts with Smad4 to repress TGF-β-induced transcriptional responses.
An AUTS2-Polycomb complex activates gene expression in the CNS.
Screen identifies bromodomain protein ZMYND8 in chromatin recognition of transcription-associated DNA damage that promotes homologous recombination.
An acetyl-methyl switch drives a conformational change in p53.
Intracellular crotonyl-CoA stimulates transcription through p300-catalyzed histone crotonylation.
Combined CSL and p53 downregulation promotes cancer-associated fibroblast activation.
PARP9-DTX3L ubiquitin ligase targets host histone H2BJ and viral 3C protease to enhance interferon signaling and control viral infection.
The LINK-A lncRNA activates normoxic HIF1α signalling in triple-negative breast cancer.
SIK2 regulates fasting-induced PPARα activity and ketogenesis through p300.
Glutamine Triggers Acetylation-Dependent Degradation of Glutamine Synthetase via the Thalidomide Receptor Cereblon.
Quantitative Mass Spectrometry Identifies Novel Host Binding Partners for Pathogenic Escherichia coli Type III Secretion System Effectors.
A Small Molecule Activator of p300/CBP Histone Acetyltransferase Promotes Survival and Neurite Growth in a Cellular Model of Parkinson's Disease.
RNA helicase DDX3 maintains lipid homeostasis through upregulation of the microsomal triglyceride transfer protein by interacting with HNF4 and SHP.
Distinct Roles of Brd2 and Brd4 in Potentiating the Transcriptional Program for Th17 Cell Differentiation.
Roles of tau protein in health and disease.
Architecture of the human interactome defines protein communities and disease networks.
p300-Mediated Lysine 2-Hydroxyisobutyrylation Regulates Glycolysis.
Dynamic Acetylation of Phosphoenolpyruvate Carboxykinase Toggles Enzyme Activity between Gluconeogenic and Anaplerotic Reactions.
Leucine Signals to mTORC1 via Its Metabolite Acetyl-Coenzyme A.
Metabolic regulation of gene expression by histone lactylation.
Leucine regulates autophagy via acetylation of the mTORC1 component raptor.
LINC00941 promotes oral squamous cell carcinoma progression via activating CAPRIN2 and canonical WNT/β-catenin signaling pathway.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Isonicotinylation is a histone mark induced by the anti-tuberculosis first-line drug isoniazid.
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
Histone H1 deamidation facilitates chromatin relaxation for DNA repair.
A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A.
The transcriptional coactivators p300 and CBP are histone acetyltransferases.
The adenovirus 12 E1A proteins can bind directly to proteins of the p300 transcription co-activator family, including the CREB-binding protein CBP and p300.
Synergistic activation of transcription by CBP and p53.
Binding and modulation of p53 by p300/CBP coactivators.
HIV-1 tat transactivator recruits p300 and CREB-binding protein histone acetyltransferases to the viral promoter.
Exogenous expression of a dominant negative RORalpha1 vector in muscle cells impairs differentiation: RORalpha1 directly interacts with p300 and myoD.
Direct suppression of Stat1 function during adenoviral infection.
Functional role of p35srj, a novel p300/CBP binding protein, during transactivation by HIF-1.
p-T,4S-IRF3:p-T,4S-IRF3:CREBBP, EP300 binds promoters of Interferon-beta
CREBBP, EP300 binds p-T,4S-IRF3:p-T,4S-IRF3
VAF/pIRF7:CBP/p300 binds the promoters of type-I IFN genes
Formation of VAF (virus-activated factor) complex
Formation of HIF:CBP:p300 complex at promoters
NICD1 in complex with RBPJ (CSL) recruits MAML
NOTCH1 PEST domain mutants coactivator complex binds CDK8:CCNC
NICD1 PEST domain mutants in complex with RBPJ (CSL) bind MAML
CDK8 phosphorylates NICD1 PEST domain mutants
Beta-catenin enhances association of IRF3 with CBP/p300
TP53 in complex with EP300, PRMT1 and CARM1 binds the GADD45A promoter
BRD7 binds TP53 and EP300
Beta-catenin recruits CBP/p300
HSF1 acetylation at Lys80
HSF1-dependent transactivation
EP300 acetylates histone H2A, H2B, H3, H4
SUMOylation of EP300 with SUMO1
FOXM1 binds CDC25A promoter
NOTCH1 Coactivator Complex binds MYC promoter
NOTCH1 Coactivator Complex binds HES5 promoter
NOTCH1 PEST domain mutants bind HES1 promoter
NOTCH1 PEST domain mutants bind MYC promoter
NOTCH1 PEST domain mutants bind HES5 promoter
NOTCH1 PEST domain mutants bind promoters of HEY genes
B-WICH recruits histone acetyltransferases
B-WICH:histone acetyltransferase acetylates histone H3 at lysine-9
C-type lectin receptors (CLRs)
BRD7 promotes EP300-mediated acetylation of TP53
p300 acetylates RELA subunit
CBP and p300 binds NF-kB complex
MYSM1 deubiquitinates Histone H2A
TP53 binds the complex of JMY, EP300 and TTC5
Regulation of TP53 Activity through Acetylation
ING2 recruits EP300 to TP53
ING2-bound EP300 acetylates TP53
TFAP2 homo- and heterodimers bind CITED and EP300/CREBBP
HIPK2 phosphorylates RUNX1 and EP300
RUNX3 binds the NOTCH1 coactivator complex
RUNX3:NOTCH1 coactivator complex binds the HES1 gene promoter
RUNX1 and GATA1 bind the promoter of the ITGA2B gene
Core MLL complex methylates H3K4Me2-Nucleosome at the ITGA2B gene promoter
RUNX1 and GATA1 bind the promoter of the GP1BA gene
Core MLL complex methylates H3K4Me2-Nucleosome at the GP1BA gene promoter
RUNX1 and GATA1 bind the promoter of the THBS1 gene
Core MLL complex methylates H3K4Me2-Nucleosome at the THBS1 gene promoter
RUNX1 and GATA1 bind the promoter of the MIR27A gene
Core MLL complex methylates H3K4Me2-Nucleosome at the MIR27A gene promoter
Acetylated RUNX3 binds to BRD2
CCND1 binds RUNX3 and displaces EP300
CITED1 and EP300 bind ESR1:estrogen:TGFA gene promoter
NCOA3 recruits EP300 to ESR1:estrogen:TFGA gene:NCOA3
Binding of AP1 transcriptional activator complexes to CCND1 promoter
EP300 is recruited to MYC and BCL2 genes
NOTCH1 coactivator complex binds NOTCH3 gene
ESR1:ESTG and EP300 are recruited to TFF3 promoter
NOTCH1,NOTCH3 coactivator complex binds PLXND1 gene promoter
HATs and coactivators are recruited to the CTSD gene
Histone acetyltransferases are recruited to the TFF1 gene
NCOA1 recruits EP300 to TGFA promoter
NCOA1 recruits EP300 to the ABCA1 promoter
GREB1 binds ESR1:ESTG and co-activators
ESR1:ESTG:PGR:P4 bind pioneer factors and coactivators
p-IRF7 dimer interacts with coactivator CBP/p300
p-S133 CREB1, LYL1 and EP300 bind the ID1 and ID3 genes
SPI1 (PU.1), PML isoform 4, and EP300 bind the promoter of the CEBPE gene
p-Y705,S727 STAT3 is acetylated
p-2S-SMAD3:p-2S-SMAD3:SMAD4 forms a complex with SP1 and EP300 at the COL1A2 gene promoter
SARS-CoV-1 N binds SMAD3 and EP300 at the SERPINE1 gene promoter
AcK-NFE2L2 binds the TXNRD1 promoter
CREBBP, EP300 acetylates NFE2L2
NFE2L2 binds CREBBP,EP300
AcK-NFE2L2 and MAFK bind the GSTA1 gene
AcK-NFE2L2 binds the GCLC gene
AcK-NFE2L2 binds the GCLM gene
AcK- NFE2L2, MAFG and CREBBP, EP300 bind the G6PD
AcK-NFE2L2 and ATF4 bind the SLC7A11 gene
NFE2L2 binds the PGD gene
p14ARF binds NFE2L2:CREBBP, EP300
AcK-NFE2L2 binds the ABCF2 gene
AcK-NFE2L2 binds the ABCG2 gene
AcK-NFE2L2 binds the SOD3 gene
AcK-NFE2L2 binds the KEAP1 gene
AcK-NFE2L2 binds the AREG gene
AcK-NFE2L2 binds the TXN gene
AcK-NFE2L2 binds the BCL2 gene
AcK-NFE2L2 binds the NOTCH1 gene
AcK-NFE2L2 binds the ABCC3 gene
AcK-NFE2L2 binds the CCL2 gene
AcK-NFE2L2 binds the ATF4 gene
AcK-NFE2L2 binds the ABCC1 gene
AcK-NFE2L2 binds the EGF gene
AcK-NFE2L2 binds the BCL2L1 gene
Coactivators are recruited to liganded PPARG:RXRA heterodimer
NFE2L2 binding to CD274 gene
MITF-M binds CREBBP,EP300
MAML recruits CDK8:CCNC to xNICD1
CDK8 phosphorylates xNICD1
mNICD1 Chimeric Enhancer Complex binds Hes1 promoter
EP300 binds SOH-C477-Foxo4
TXN disrupts Foxo4 comples with EP300
The structural basis of protein acetylation by the p300/CBP transcriptional coactivator.
Different functional modes of p300 in activation of RNA polymerase III transcription from chromatin templates.
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
SET1 and p300 Act Synergistically, through Coupled Histone Modifications, in Transcriptional Activation by p53.
Corrigendum: Combined CSL and p53 downregulation promotes cancer-associated fibroblast activation.
Arginine methyltransferase CARM1 is a promoter-specific regulator of NF-kappaB-dependent gene expression.
Pitx2 is functionally important in the early stages of vascular smooth muscle cell differentiation.
Stress-inducible regulation of heat shock factor 1 by the deacetylase SIRT1.
Syndromic features and mild cognitive impairment in mice with genetic reduction on p300 activity: Differential contribution of p300 and CBP to Rubinstein-Taybi syndrome etiology.
Regulation of unfolded protein response modulator XBP1s by acetylation and deacetylation.
The methyltransferase SMYD3 mediates the recruitment of transcriptional cofactors at the myostatin and c-Met genes and regulates skeletal muscle atrophy.
p300-dependent acetylation of activating transcription factor 5 enhances C/EBPβ transactivation of C/EBPα during 3T3-L1 differentiation.
A SIRT7-dependent acetylation switch of GABPβ1 controls mitochondrial function.
Dynamic Competing Histone H4 K5K8 Acetylation and Butyrylation Are Hallmarks of Highly Active Gene Promoters.
BCAA-BCKA axis regulates WAT browning through acetylation of PRDM16.
Mammalian GCN5 and P/CAF acetyltransferases have homologous amino-terminal domains important for recognition of nucleosomal substrates.