scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.272.9.5571 |
P698 | PubMed publication ID | 9038164 |
P50 | author | Ayman M Saleh | Q46640792 |
P2093 | author name string | R Cook | |
V Lang | |||
C J Brandl | |||
P2860 | cites work | Identification of human proteins functionally conserved with the yeast putative adaptors ADA2 and GCN5 | Q24315711 |
Purification of a RAS-responsive adenylyl cyclase complex from Saccharomyces cerevisiae by use of an epitope addition method | Q24631695 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product | Q27860841 | ||
ADA3, a putative transcriptional adaptor, consists of two separable domains and interacts with ADA2 and GCN5 in a trimeric complex | Q27930121 | ||
ADA5/SPT20 links the ADA and SPT genes, which are involved in yeast transcription | Q27932447 | ||
TFIIF-TAF-RNA polymerase II connection | Q27932651 | ||
SSN genes that affect transcriptional repression in Saccharomyces cerevisiae encode SIN4, ROX3, and SRB proteins associated with RNA polymerase II | Q27933314 | ||
Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast | Q27933378 | ||
Yeast ADA2 protein binds to the VP16 protein activation domain and activates transcription. | Q27935228 | ||
RNA polymerase II subunit RPB3 is an essential component of the mRNA transcription apparatus | Q27936059 | ||
SNF11, a new component of the yeast SNF-SWI complex that interacts with a conserved region of SNF2. | Q27937070 | ||
Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation | Q27937778 | ||
New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites | Q28131597 | ||
A positive selection for mutants lacking orotidine-5'-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance | Q28131606 | ||
Genetic isolation of ADA2: a potential transcriptional adaptor required for function of certain acidic activation domains | Q29620928 | ||
The RNA polymerase II holoenzyme and its implications for gene regulation | Q29622942 | ||
Saturation mutagenesis of a yeast his3 "TATA element": genetic evidence for a specific TATA-binding protein | Q33567358 | ||
Yeast global transcriptional regulators Sin4 and Rgr1 are components of mediator complex/RNA polymerase II holoenzyme. | Q33739221 | ||
Mutations in RNA polymerase II enhance or suppress mutations in GAL4. | Q33850755 | ||
Identification and characterization of a TFIID-like multiprotein complex from Saccharomyces cerevisiae | Q33958879 | ||
GAL4 interacts with TATA-binding protein and coactivators | Q34309986 | ||
Paf1p, an RNA polymerase II-associated factor in Saccharomyces cerevisiae, may have both positive and negative roles in transcription | Q36557179 | ||
Analysis of Saccharomyces cerevisiae his3 transcription in vitro: biochemical support for multiple mechanisms of transcription | Q36710678 | ||
ADA3: a gene, identified by resistance to GAL4-VP16, with properties similar to and different from those of ADA2. | Q36822602 | ||
Specific initiation by RNA polymerase I in a whole-cell extract from yeast | Q37391358 | ||
Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast | Q37539289 | ||
Structural and functional analysis of yeast putative adaptors. Evidence for an adaptor complex in vivo | Q38361167 | ||
SPT20/ADA5 encodes a novel protein functionally related to the TATA-binding protein and important for transcription in Saccharomyces cerevisiae | Q40019111 | ||
Common themes in assembly and function of eukaryotic transcription complexes | Q40422045 | ||
The SNF/SWI family of global transcriptional activators | Q40626454 | ||
TBP-TAF complexes: selectivity factors for eukaryotic transcription | Q40626459 | ||
Transcriptional activation by yeast PDR1p is inhibited by its association with NGG1p/ADA3p | Q48062271 | ||
Genetic evidence for the interaction of the yeast transcriptional co-activator proteins GCN5 and ADA2. | Q52511808 | ||
Structure/functional properties of the yeast dual regulator protein NGG1 that are required for glucose repression. | Q52519385 | ||
Yeast TAFIIS in a multisubunit complex required for activated transcription. | Q52541518 | ||
Characterization of Physical Interactions of the Putative Transcriptional Adaptor, ADA2, with Acidic Activation Domains and TATA-binding Protein | Q58130306 | ||
DNA-binding properties of the yeast SWI/SNF complex | Q59068266 | ||
RNA polymerase II holoenzyme contains SWI/SNF regulators involved in chromatin remodeling | Q70908581 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 5571-5578 | |
P577 | publication date | 1997-02-01 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Identification of native complexes containing the yeast coactivator/repressor proteins NGG1/ADA3 and ADA2 | |
P478 | volume | 272 |
Q41653844 | A SAGA of histone acetylation and gene expression |
Q22011164 | A novel TATA-binding protein-binding protein, ABT1, activates basal transcription and has a yeast homolog that is essential for growth |
Q24682174 | A novel human Ada2 homologue functions with Gcn5 or Brg1 to coactivate transcription |
Q27936635 | A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation |
Q24650997 | A systematic screen for transcriptional regulators of the yeast cell cycle |
Q27939725 | ADA1, a novel component of the ADA/GCN5 complex, has broader effects than GCN5, ADA2, or ADA3. |
Q24530010 | ADA3-containing complexes associate with estrogen receptor alpha |
Q60909339 | Acceptor Stem Differences Contribute to Species-Specific Use of Yeast and Human tRNA |
Q24548503 | Acetylation of histones and transcription-related factors |
Q27934769 | Analysis of Spt7 function in the Saccharomyces cerevisiae SAGA coactivator complex. |
Q33293626 | C-terminal processing of yeast Spt7 occurs in the absence of functional SAGA complex |
Q30448772 | Cell cycle-regulated histone acetylation required for expression of the yeast HO gene |
Q36416226 | Characterization of new Spt3 and TATA-binding protein mutants of Saccharomyces cerevisiae: Spt3 TBP allele-specific interactions and bypass of Spt8. |
Q24798328 | Characterization of yeast histone H3-specific type B histone acetyltransferases identifies an ADA2-independent Gcn5p activity |
Q35748234 | Chromatin and transcription in yeast |
Q77570570 | Chromatin remodeling: a marriage between two families? |
Q27937089 | Cluster analysis of mass spectrometry data reveals a novel component of SAGA |
Q27932566 | Combinatorial depletion analysis to assemble the network architecture of the SAGA and ADA chromatin remodeling complexes |
Q34281088 | Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium |
Q33847058 | Contribution of CgPDR1-regulated genes in enhanced virulence of azole-resistant Candida glabrata |
Q35193069 | Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo |
Q28575519 | Deregulated expression of a novel component of TFTC/STAGA histone acetyltransferase complexes, rat SGF29, in hepatocellular carcinoma: possible implication for the oncogenic potential of c-Myc |
Q33970848 | Essential functional interactions of SAGA, a Saccharomyces cerevisiae complex of Spt, Ada, and Gcn5 proteins, with the Snf/Swi and Srb/mediator complexes |
Q27930736 | Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction. |
Q33529002 | GCN5 is a positive regulator of origins of DNA replication in Saccharomyces cerevisiae |
Q43977755 | Gal80 confers specificity on HAT complex interactions with activators |
Q27929940 | Histone H3 specific acetyltransferases are essential for cell cycle progression |
Q35192911 | Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo |
Q33959141 | Histone acetyltransferase complexes can mediate transcriptional activation by the major glucocorticoid receptor activation domain |
Q28202210 | Human papilloma virus 16 E6 oncoprotein inhibits retinoic X receptor-mediated transactivation by targeting human ADA3 coactivator |
Q24537722 | Human papillomavirus oncoprotein E6 inactivates the transcriptional coactivator human ADA3 |
Q44900828 | Identification and analysis of native HAT complexes. |
Q27931284 | Identification of two novel TAF subunits of the yeast Saccharomyces cerevisiae TFIID complex |
Q27938704 | Inhibition of TATA-binding protein function by SAGA subunits Spt3 and Spt8 at Gcn4-activated promoters |
Q27939381 | Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p |
Q36216047 | Mammalian alteration/deficiency in activation 3 (Ada3) is essential for embryonic development and cell cycle progression |
Q29620260 | Molecular genetics of the RNA polymerase II general transcriptional machinery |
Q27930623 | Mutational analysis of the C-terminal FATC domain of Saccharomyces cerevisiae Tra1. |
Q42664605 | Mutations in both the structured domain and N-terminus of histone H2B bypass the requirement for Swi-Snf in yeast |
Q36155203 | Nucleosome competition reveals processive acetylation by the SAGA HAT module. |
Q42002467 | Nucleosome structure of the yeast CHA1 promoter: analysis of activation-dependent chromatin remodeling of an RNA-polymerase-II-transcribed gene in TBP and RNA pol II mutants defective in vivo in response to acidic activators. |
Q33911284 | Phosphorylation of serine 10 in histone H3 is functionally linked in vitro and in vivo to Gcn5-mediated acetylation at lysine 14. |
Q27933987 | Positive and negative functions of the SAGA complex mediated through interaction of Spt8 with TBP and the N-terminal domain of TFIIA. |
Q27931371 | Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometry |
Q35206109 | Recruitment of the SWI/SNF chromatin remodeling complex by transcriptional activators |
Q40023668 | Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression |
Q27937005 | Rpm2p, a component of yeast mitochondrial RNase P, acts as a transcriptional activator in the nucleus |
Q27936016 | SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcription |
Q39452532 | SWI-SNF-mediated nucleosome remodeling: role of histone octamer mobility in the persistence of the remodeled state |
Q41580909 | Structure/function analysis of the phosphatidylinositol-3-kinase domain of yeast tra1. |
Q27932073 | Systematic genetic array analysis links the Saccharomyces cerevisiae SAGA/SLIK and NuA4 component Tra1 to multiple cellular processes |
Q27931014 | The ADA complex is a distinct histone acetyltransferase complex in Saccharomyces cerevisiae |
Q27937594 | The ATM-related cofactor Tra1 is a component of the purified SAGA complex |
Q27937771 | The C-terminal residues of Saccharomyces cerevisiae Mec1 are required for its localization, stability, and function |
Q41077086 | The Drosophila histone acetyltransferase Gcn5 and transcriptional adaptor Ada2a are involved in nucleosomal histone H4 acetylation |
Q33772811 | The Gcn4p activation domain interacts specifically in vitro with RNA polymerase II holoenzyme, TFIID, and the Adap-Gcn5p coactivator complex |
Q28513184 | The PCAF acetylase complex as a potential tumor suppressor |
Q35070043 | The PS1 hairpin of Mcm3 is essential for viability and for DNA unwinding in vitro |
Q52329552 | The Pseudokinase Domain of Saccharomyces cerevisiae Tra1 Is Required for Nuclear Localization and Incorporation into the SAGA and NuA4 Complexes. |
Q42459431 | The SAGA unfolds: convergence of transcription regulators in chromatin-modifying complexes. |
Q24554343 | The essential cofactor TRRAP recruits the histone acetyltransferase hGCN5 to c-Myc |
Q27934606 | The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway. |
Q27930726 | The something about silencing protein, Sas3, is the catalytic subunit of NuA3, a yTAF(II)30-containing HAT complex that interacts with the Spt16 subunit of the yeast CP (Cdc68/Pob3)-FACT complex |
Q35199113 | The yeast Ada complex mediates the ligand-dependent activation function AF-2 of retinoid X and estrogen receptors |
Q73821749 | The yeast histone acetyltransferase A2 complex, but not free Gcn5p, binds stably to nucleosomal arrays |
Q27936339 | Transcriptional activation by Gcn4p involves independent interactions with the SWI/SNF complex and the SRB/mediator |
Q89709144 | Whitefly HES1 binds to the intergenic region of Tomato yellow leaf curl China virus and promotes viral gene transcription |
Q29622932 | Yeast carbon catabolite repression |
Q27940108 | Yeast enhancer of polycomb defines global Esa1-dependent acetylation of chromatin. |
Q27935097 | Yng1p modulates the activity of Sas3p as a component of the yeast NuA3 Hhistone acetyltransferase complex |
Q77652532 | yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex |
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