scholarly article | Q13442814 |
P2093 | author name string | Michael R Green | |
Sukesh R Bhaumik | |||
P2860 | cites work | Characterization of a human homologue of the Saccharomyces cerevisiae transcription factor spt3 (SUPT3H) | Q22004008 |
ADA3, a putative transcriptional adaptor, consists of two separable domains and interacts with ADA2 and GCN5 in a trimeric complex | Q27930121 | ||
Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction. | Q27930736 | ||
Distinct classes of yeast promoters revealed by differential TAF recruitment | Q27931136 | ||
Recruitment of HAT complexes by direct activator interactions with the ATM-related Tra1 subunit | Q27933602 | ||
Yeast Gcn5 functions in two multisubunit complexes to acetylate nucleosomal histones: characterization of an Ada complex and the SAGA (Spt/Ada) complex | Q27934812 | ||
Distinct mutations in yeast TAF(II)25 differentially affect the composition of TFIID and SAGA complexes as well as global gene expression patterns. | Q27936344 | ||
A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation | Q27937778 | ||
Inhibition of TATA-binding protein function by SAGA subunits Spt3 and Spt8 at Gcn4-activated promoters | Q27938704 | ||
Role of the Ada2 and Ada3 transcriptional coactivators in histone acetylation | Q27939467 | ||
TAF-Containing and TAF-independent forms of transcriptionally active TBP in vivo. | Q27939707 | ||
ADA1, a novel component of the ADA/GCN5 complex, has broader effects than GCN5, ADA2, or ADA3. | Q27939725 | ||
The S. cerevisiae SAGA complex functions in vivo as a coactivator for transcriptional activation by Gal4. | Q27940298 | ||
SAGA is an essential in vivo target of the yeast acidic activator Gal4p | Q28345347 | ||
Regulation of gene expression by TBP-associated proteins | Q28679170 | ||
Histone acetyltransferases | Q29547823 | ||
Genetic isolation of ADA2: a potential transcriptional adaptor required for function of certain acidic activation domains | Q29620928 | ||
TAFs revisited: more data reveal new twists and confirm old ideas | Q30587319 | ||
The SAGA of Spt proteins and transcriptional analysis in yeast: past, present, and future | Q33671553 | ||
The many HATs of transcription coactivators | Q33818804 | ||
TBP-associated factors (TAFIIs): multiple, selective transcriptional mediators in common complexes | Q33832058 | ||
Histone acetyltransferase activity and interaction with ADA2 are critical for GCN5 function in vivo. | Q33886079 | ||
The Saccharomyces cerevisiae SPT8 gene encodes a very acidic protein that is functionally related to SPT3 and TATA-binding protein | Q33963168 | ||
Essential functional interactions of SAGA, a Saccharomyces cerevisiae complex of Spt, Ada, and Gcn5 proteins, with the Snf/Swi and Srb/mediator complexes | Q33970848 | ||
Transcriptional activation in yeast cells lacking transcription factor IIA. | Q34608335 | ||
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 | ||
Redundant roles for the TFIID and SAGA complexes in global transcription | Q38311191 | ||
Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA. | Q38330677 | ||
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 | ||
Functional similarity and physical association between GCN5 and ADA2: putative transcriptional adaptors. | Q40793485 | ||
Promoter specificity of basal transcription factors | Q41634308 | ||
A SAGA of histone acetylation and gene expression | Q41653844 | ||
The SAGA unfolds: convergence of transcription regulators in chromatin-modifying complexes. | Q42459431 | ||
Identification and analysis of homologues of Saccharomyces cerevisiae Spt3 suggest conserved functional domains | Q48038615 | ||
A unified nomenclature for TATA box binding protein (TBP)-associated factors (TAFs) involved in RNA polymerase II transcription | Q48733526 | ||
SPT3 interacts with TFIID to allow normal transcription in Saccharomyces cerevisiae | Q68203604 | ||
Histone-like TAFs are essential for transcription in vivo | Q77652527 | ||
yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex | Q77652532 | ||
P433 | issue | 21 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
SAGA complex subunit SPT8 YLR055C | Q27550490 | ||
Transcriptional regulator SPT3 YDR392W | Q27552859 | ||
P304 | page(s) | 7365-7371 | |
P577 | publication date | 2002-11-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Differential requirement of SAGA components for recruitment of TATA-box-binding protein to promoters in vivo | |
P478 | volume | 22 |