scholarly article | Q13442814 |
P2093 | author name string | Yang Liu | |
Yan Zhao | |||
Min-Hao Kuo | |||
Xinjing Xu | |||
Soumya Singh-Rodriguez | |||
P2860 | cites work | Structure and ligand of a histone acetyltransferase bromodomain | Q22009928 |
Repression of GCN5 histone acetyltransferase activity via bromodomain-mediated binding and phosphorylation by the Ku-DNA-dependent protein kinase complex | Q24522344 | ||
Crystal structure of the histone acetyltransferase domain of the human PCAF transcriptional regulator bound to coenzyme A | Q27618906 | ||
Solution structure of the catalytic domain of GCN5 histone acetyltransferase bound to coenzyme A | Q27618997 | ||
Crystal structure and mechanism of histone acetylation of the yeast GCN5 transcriptional coactivator | Q27619265 | ||
Structure of Tetrahymena GCN5 bound to coenzyme A and a histone H3 peptide | Q27619606 | ||
Structure and function of a human TAFII250 double bromodomain module | Q27622657 | ||
SPT3 interacts with TFIID to allow normal transcription in Saccharomyces cerevisiae | Q68203604 | ||
Mitosis-specific histone H3 phosphorylation in vitro in nucleosome structures | Q68921418 | ||
Three-dimensional structure of the human TFIID-IIA-IIB complex | Q73257310 | ||
Gcn4 activator targets Gcn5 histone acetyltransferase to specific promoters independently of transcription | Q73406568 | ||
Kinetic mechanism of the histone acetyltransferase GCN5 from yeast | Q73794124 | ||
Transposon mutagenesis for the analysis of protein production, function, and localization | Q77815537 | ||
Catalytic mechanism and function of invariant glutamic acid 173 from the histone acetyltransferase GCN5 transcriptional coactivator | Q77895379 | ||
Structural Basis for Histone and Phosphohistone Binding by the GCN5 Histone Acetyltransferase | Q27642329 | ||
A generic protein purification method for protein complex characterization and proteome exploration | Q27861087 | ||
Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo | Q27930390 | ||
Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction. | Q27930736 | ||
An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p | Q27932320 | ||
Protein phosphatase type 1 regulates ion homeostasis in Saccharomyces cerevisiae. | Q27932578 | ||
Functional analysis of the yeast Glc7-binding protein Reg1 identifies a protein phosphatase type 1-binding motif as essential for repression of ADH2 expression | Q27932585 | ||
Sip2, an N-myristoylated beta subunit of Snf1 kinase, regulates aging in Saccharomyces cerevisiae by affecting cellular histone kinase activity, recombination at rDNA loci, and silencing | Q27932945 | ||
Srb/mediator proteins interact functionally and physically with transcriptional repressor Sfl1. | Q27933861 | ||
Transcriptional activation via sequential histone H2B ubiquitylation and deubiquitylation, mediated by SAGA-associated Ubp8. | Q27933975 | ||
The REG2 gene of Saccharomyces cerevisiae encodes a type 1 protein phosphatase-binding protein that functions with Reg1p and the Snf1 protein kinase to regulate growth | Q27934083 | ||
The novel SLIK histone acetyltransferase complex functions in the yeast retrograde response pathway. | Q27934606 | ||
Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex | Q27934812 | ||
Molecular analysis of the SNF4 gene of Saccharomyces cerevisiae: evidence for physical association of the SNF4 protein with the SNF1 protein kinase | Q27934940 | ||
Different sensitivities of bromodomain factors 1 and 2 to histone H4 acetylation | Q27935667 | ||
SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcription | Q27936016 | ||
A protein kinase substrate identified by the two-hybrid system | Q27936243 | ||
A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
Sterile 20 kinase phosphorylates histone H2B at serine 10 during hydrogen peroxide-induced apoptosis in S. cerevisiae | Q27936975 | ||
Bromodomains mediate an acetyl-histone encoded antisilencing function at heterochromatin boundaries | Q27937031 | ||
Chd1 chromodomain links histone H3 methylation with SAGA- and SLIK-dependent acetylation | Q27937996 | ||
A Gip1p-Glc7p phosphatase complex regulates septin organization and spore wall formation. | Q27938217 | ||
Inhibition of TATA-binding protein function by SAGA subunits Spt3 and Spt8 at Gcn4-activated promoters | Q27938704 | ||
H2B ubiquitin protease Ubp8 and Sgf11 constitute a discrete functional module within the Saccharomyces cerevisiae SAGA complex. | Q27939759 | ||
Protein phosphatase type 1 interacts with proteins required for meiosis and other cellular processes in Saccharomyces cerevisiae | Q27939890 | ||
The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4. | Q27940298 | ||
New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites | Q28131597 | ||
New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications | Q28131600 | ||
Getting started with yeast | Q28131602 | ||
Improved method for high efficiency transformation of intact yeast cells | Q28131608 | ||
Dissecting the regulatory circuitry of a eukaryotic genome | Q28131632 | ||
Synergistic coupling of histone H3 phosphorylation and acetylation in response to epidermal growth factor stimulation | Q28141828 | ||
Aurora-B phosphorylates Histone H3 at serine28 with regard to the mitotic chromosome condensation | Q28202615 | ||
SRN1, a yeast gene involved in RNA processing, is identical to HEX2/REG1, a negative regulator in glucose repression | Q36817251 | ||
Glucose-regulated interaction of a regulatory subunit of protein phosphatase 1 with the Snf1 protein kinase in Saccharomyces cerevisiae | Q37393837 | ||
Activation of the Saccharomyces cerevisiae Heat Shock Transcription Factor Under Glucose Starvation Conditions by Snf1 Protein Kinase | Q38348172 | ||
The Reg1-interacting proteins, Bmh1, Bmh2, Ssb1, and Ssb2, have roles in maintaining glucose repression in Saccharomyces cerevisiae | Q39379140 | ||
Three-dimensional structures of the TAFII-containing complexes TFIID and TFTC. | Q39524270 | ||
Multiple Mechanistically Distinct Functions of SAGA at the PHO5 Promoter | Q39787518 | ||
Recessive mutations conferring resistance to carbon catabolite repression of galactokinase synthesis in Saccharomyces cerevisiae | Q39988768 | ||
Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression | Q40023668 | ||
lacZY gene fusion cassettes with KanR resistance | Q40545550 | ||
REG1 binds to protein phosphatase type 1 and regulates glucose repression in Saccharomyces cerevisiae. | Q40790102 | ||
Molecular requirements for gene expression mediated by targeted histone acetyltransferases | Q41296285 | ||
Glucose repression of yeast mitochondrial transcription: kinetics of derepression and role of nuclear genes | Q41836856 | ||
Molecular architecture of the S. cerevisiae SAGA complex. | Q42631699 | ||
Functional interaction between GCN5 and polyamines: a new role for core histone acetylation | Q42684462 | ||
Genetic and molecular characterization of GAL83: its interaction and similarities with other genes involved in glucose repression in Saccharomyces cerevisiae. | Q42964331 | ||
Mutational analysis of conserved residues in the GCN5 family of histone acetyltransferases | Q43633793 | ||
Snf1--a histone kinase that works in concert with the histone acetyltransferase Gcn5 to regulate transcription. | Q43703058 | ||
A tethered catalysis, two-hybrid system to identify protein-protein interactions requiring post-translational modifications | Q47315021 | ||
A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae | Q48017973 | ||
The 14-3-3 proteins encoded by the BMH1 and BMH2 genes are essential in the yeast Saccharomyces cerevisiae and can be replaced by a plant homologue | Q48074840 | ||
Characterization of Hex2 protein, a negative regulatory element necessary for glucose repression in yeast | Q48211763 | ||
Multiple regulatory proteins mediate repression and activation by interaction with the yeast Mig1 binding site | Q58500327 | ||
Roles of histone acetyltransferases and deacetylases in gene regulation | Q28286019 | ||
Phosphorylation of Ser28 in histone H3 mediated by mixed lineage kinase-like mitogen-activated protein triple kinase alpha | Q28305184 | ||
SAGA is an essential in vivo target of the yeast acidic activator Gal4p | Q28345347 | ||
Increasing the rate of chromatin remodeling and gene activation--a novel role for the histone acetyltransferase Gcn5 | Q28348534 | ||
Histone acetyltransferases | Q29547823 | ||
The AMP-activated/SNF1 protein kinase subfamily: metabolic sensors of the eukaryotic cell? | Q29618125 | ||
Yeast Saccharomyces cerevisiae selectable markers in pUC18 polylinkers | Q29620747 | ||
Cell cycle-regulated histone acetylation required for expression of the yeast HO gene | Q30448772 | ||
Regulatory interactions between the Reg1-Glc7 protein phosphatase and the Snf1 protein kinase | Q30453592 | ||
Deubiquitination of histone H2B by a yeast acetyltransferase complex regulates transcription. | Q33195734 | ||
Snf1 protein kinase regulates phosphorylation of the Mig1 repressor in Saccharomyces cerevisiae | Q33781305 | ||
Phosphorylation of serine 10 in histone H3 is functionally linked in vitro and in vivo to Gcn5-mediated acetylation at lysine 14. | Q33911284 | ||
Histone H3 phosphorylation can promote TBP recruitment through distinct promoter-specific mechanisms | Q33930752 | ||
Mutations causing constitutive invertase synthesis in yeast: genetic interactions with snf mutations | Q33952793 | ||
Genetic interactions between REG1/HEX2 and GLC7, the gene encoding the protein phosphatase type 1 catalytic subunit in Saccharomyces cerevisiae | Q33967254 | ||
Essential functional interactions of SAGA, a Saccharomyces cerevisiae complex of Spt, Ada, and Gcn5 proteins, with the Snf/Swi and Srb/mediator complexes | Q33970848 | ||
The diverse functions of histone acetyltransferase complexes. | Q34205129 | ||
Components of the SAGA histone acetyltransferase complex are required for repressed transcription of ARG1 in rich medium | Q34281088 | ||
Evidence that Spt10 and Spt21 of Saccharomyces cerevisiae play distinct roles in vivo and functionally interact with MCB-binding factor, SCB-binding factor and Snf1. | Q34573307 | ||
Evidence for the involvement of the Glc7-Reg1 phosphatase and the Snf1-Snf4 kinase in the regulation of INO1 transcription in Saccharomyces cerevisiae | Q34606906 | ||
Analysis of the mechanism by which glucose inhibits maltose induction of MAL gene expression in Saccharomyces. | Q34608632 | ||
Regulation of TATA-binding protein binding by the SAGA complex and the Nhp6 high-mobility group protein. | Q34740357 | ||
Transcriptional control of nonfermentative metabolism in the yeast Saccharomyces cerevisiae | Q35114839 | ||
A regulatory shortcut between the Snf1 protein kinase and RNA polymerase II holoenzyme | Q35171792 | ||
Histone acetyltransferase activity of yeast Gcn5p is required for the activation of target genes in vivo | Q35192911 | ||
Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo | Q35193069 | ||
The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo | Q35209265 | ||
Highly conserved protein kinases involved in the regulation of carbon and amino acid metabolism. | Q35596462 | ||
Regulation of the proteinase B structural gene PRB1 in Saccharomyces cerevisiae | Q35620313 | ||
Histones and histone modifications | Q35842800 | ||
SAGA unveiled. | Q36011032 | ||
GCN5-dependent histone H3 acetylation and RPD3-dependent histone H4 deacetylation have distinct, opposing effects on IME2 transcription, during meiosis and during vegetative growth, in budding yeast | Q36383484 | ||
ADH2 expression is repressed by REG1 independently of mutations that alter the phosphorylation of the yeast transcription factor ADR1 | Q36691489 | ||
Two systems of glucose repression of the GAL1 promoter in Saccharomyces cerevisiae | Q36724367 | ||
P433 | issue | 23 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phosphorylation | Q242736 |
P304 | page(s) | 10566-10579 | |
P577 | publication date | 2005-12-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Histone H3 Ser10 phosphorylation-independent function of Snf1 and Reg1 proteins rescues a gcn5- mutant in HIS3 expression | |
P478 | volume | 25 |
Q47292240 | A Failsafe for Sensing Chromatid Tension in Mitosis with the Histone H3 Tail in Saccharomyces cerevisiae |
Q27938869 | A chemical genomics study identifies Snf1 as a repressor of GCN4 translation |
Q34799669 | Activator-independent transcription of Snf1-dependent genes in mutants lacking histone tails |
Q44778228 | C-terminus of the Sgf73 subunit of SAGA and SLIK is important for retention in the larger complex and for heterochromatin boundary function. |
Q34478777 | Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID |
Q35024989 | FSH signaling pathways in immature granulosa cells that regulate target gene expression: branching out from protein kinase A. |
Q37468898 | Functional connection between histone acetyltransferase Gcn5p and methyltransferase Hmt1p |
Q27932530 | H4 acetylation does not replace H3 acetylation in chromatin remodelling and transcription activation of Adr1-dependent genes. |
Q33558797 | Histone h3 exerts a key function in mitotic checkpoint control |
Q42741230 | Identification of Tension Sensing Motif of Histone H3 in Saccharomyces cerevisiae and Its Regulation by Histone Modifying Enzymes |
Q34994779 | Mitogen- and stress-activated protein kinase 1-induced neuroprotection in Huntington's disease: role on chromatin remodeling at the PGC-1-alpha promoter. |
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Q34374051 | N-terminal domain of nuclear IL-1α shows structural similarity to the C-terminal domain of Snf1 and binds to the HAT/core module of the SAGA complex. |
Q39446245 | Network reconstruction and validation of the Snf1/AMPK pathway in baker's yeast based on a comprehensive literature review |
Q36992466 | SNF1/AMPK pathways in yeast |
Q33877596 | Snf1 promotes phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 by activating Gcn2 and inhibiting phosphatases Glc7 and Sit4. |
Q33628559 | Snf1p regulates Gcn5p transcriptional activity by antagonizing Spt3p |
Q44309963 | The mitogen-activated protein kinase Slt2 modulates arsenite transport through the aquaglyceroporin Fps1. |
Q37336113 | The yeast AMPK homolog SNF1 regulates acetyl coenzyme A homeostasis and histone acetylation |
Q58132508 | YHMI: a web tool to identify histone modifications and histone/chromatin regulators from a gene list in yeast |
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