scholarly article | Q13442814 |
P2093 | author name string | Arnold J Berk | |
Helen J Brown | |||
Lisa S Martel | |||
P2860 | cites work | Cloning and expression of human TAFII250: a TBP-associated factor implicated in cell-cycle regulation | Q24308057 |
TAFII250 is a bipartite protein kinase that phosphorylates the base transcription factor RAP74 | Q24309172 | ||
The TAF(II)250 subunit of TFIID has histone acetyltransferase activity | Q24310327 | ||
Cloning and biochemical characterization of TAF-172, a human homolog of yeast Mot1. | Q24314747 | ||
Histone-like TAFs within the PCAF histone acetylase complex | Q24317520 | ||
Structure and function of a human transcription factor TFIIIB subunit that is evolutionarily conserved and contains both TFIIB- and high-mobility-group protein 2-related domains | Q24320187 | ||
Cloning of the cDNA for the TATA-binding protein-associated factorII170 subunit of transcription factor B-TFIID reveals homology to global transcription regulators in yeast and Drosophila | Q24320216 | ||
Reconstitution of transcription factor SL1: exclusive binding of TBP by SL1 or TFIID subunits | Q24336167 | ||
Molecular cloning of the small (gamma) subunit of human TFIIA reveals functions critical for activated transcription | Q24336744 | ||
DNA binding site selection by RNA polymerase II TAFs: a TAF(II)250-TAF(II)150 complex recognizes the initiator | Q24534381 | ||
Positive and negative TAF(II) functions that suggest a dynamic TFIID structure and elicit synergy with traps in activator-induced transcription | Q24548316 | ||
Composition of transcription factor B-TFIID | Q24564149 | ||
Protein-protein interactions in eukaryotic transcription initiation: structure of the preinitiation complex | Q24567655 | ||
The human CCG1 gene, essential for progression of the G1 phase, encodes a 210-kilodalton nuclear DNA-binding protein | Q24601947 | ||
Structure and function of a human TAFII250 double bromodomain module | Q27622657 | ||
Crystal structure of negative cofactor 2 recognizing the TBP-DNA transcription complex | Q27633373 | ||
Crystal structure of a yeast TBP/TATA-box complex | Q27732067 | ||
Crystal structure of a yeast TFIIA/TBP/DNA complex | Q27732643 | ||
Crystal structure of a human TATA box-binding protein/TATA element complex | Q27732747 | ||
How proteins recognize the TATA box | Q27733301 | ||
Solution structure of a TBP-TAF(II)230 complex: protein mimicry of the minor groove surface of the TATA box unwound by TBP | Q27765345 | ||
Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei | Q27860728 | ||
The histone H3-like TAF is broadly required for transcription in yeast | Q27930236 | ||
A multiprotein mediator of transcriptional activation and its interaction with the C-terminal repeat domain of RNA polymerase II. | Q27930548 | ||
Distinct classes of yeast promoters revealed by differential TAF recruitment | Q27931136 | ||
A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation | Q27936635 | ||
TAF-Containing and TAF-independent forms of transcriptionally active TBP in vivo. | Q27939707 | ||
Cloning of a transcriptionally active human TATA binding factor | Q28118101 | ||
Transcription factor IIA derepresses TATA-binding protein (TBP)-associated factor inhibition of TBP-DNA binding | Q28272088 | ||
TBP, a universal eukaryotic transcription factor? | Q28626484 | ||
TAFs mediate transcriptional activation and promoter selectivity | Q29616441 | ||
The role of general initiation factors in transcription by RNA polymerase II | Q29616442 | ||
Five intermediate complexes in transcription initiation by RNA polymerase II | Q29616444 | ||
GAL4-VP16 is an unusually potent transcriptional activator | Q29616453 | ||
An RNA polymerase II holoenzyme responsive to activators | Q29620210 | ||
A TATA-binding protein mutant defective for TFIID complex formation in vivo | Q33651485 | ||
The yeast TAF145 inhibitory domain and TFIIA competitively bind to TATA-binding protein | Q33771547 | ||
Region of yeast TAF 130 required for TFIID to associate with promoters | Q34011585 | ||
The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAFII60 of Drosophila | Q35196382 | ||
TFIID-specific yeast TAF40 is essential for the majority of RNA polymerase II-mediated transcription in vivo | Q35207267 | ||
The yeast TATA-binding protein (TBP) core domain assembles with human TBP-associated factors into a functional TFIID complex | Q36567235 | ||
Radical mutations reveal TATA-box binding protein surfaces required for activated transcription in vivo. | Q36823841 | ||
Identification of human TFIID components and direct interaction between a 250-kDa polypeptide and the TATA box-binding protein (TFIID tau). | Q37340188 | ||
High affinity interaction of yeast transcriptional regulator, Mot1, with TATA box-binding protein (TBP). | Q38302607 | ||
Holo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter | Q38325574 | ||
Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA. | Q38330677 | ||
TAF(II)170 interacts with the concave surface of TATA-binding protein to inhibit its DNA binding activity | Q39528791 | ||
Polymerase (Pol) III TATA box-binding protein (TBP)-associated factor Brf binds to a surface on TBP also required for activated Pol II transcription | Q39574692 | ||
Structure-function analysis of TAF130: identification and characterization of a high-affinity TATA-binding protein interaction domain in the N terminus of yeast TAF(II)130 | Q40022288 | ||
Residues in the TATA-binding protein required to mediate a transcriptional response to retinoic acid in EC cells | Q41521246 | ||
TAFII-independent activation mediated by human TBP in the presence of the positive cofactor PC4 | Q42459088 | ||
Yeast and human TFIID with altered DNA-binding specificity for TATA elements | Q42468243 | ||
Coactivators for a proline-rich activator purified from the multisubunit human TFIID complex | Q42468497 | ||
The yeast general transcription factor TFIIA is composed of two polypeptide subunits. | Q42473274 | ||
Assembly of recombinant TFIID reveals differential coactivator requirements for distinct transcriptional activators | Q42491732 | ||
Multiple regions of TBP participate in the response to transcriptional activators in vivo | Q42492940 | ||
Identification of TFIID components required for transcriptional activation by upstream stimulatory factor. | Q42506419 | ||
TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
TAF25p, a non-histone-like subunit of TFIID and SAGA complexes, is essential for total mRNA gene transcription in vivo | Q42604308 | ||
Drosophila 230-kD TFIID subunit, a functional homolog of the human cell cycle gene product, negatively regulates DNA binding of the TATA box-binding subunit of TFIID. | Q42623034 | ||
A new regulatory domain on the TATA-binding protein | Q42688009 | ||
Largest subunit of Drosophila transcription factor IID directs assembly of a complex containing TBP and a coactivator. | Q44826917 | ||
Physical Analysis of Transcription Preinitiation Complex Assembly on a Class II Gene Promoter | Q45226839 | ||
Factors (TAFs) required for activated transcription interact with TATA box-binding protein conserved core domain. | Q45934754 | ||
Transcription activation via enhanced preinitiation complex assembly in a human cell-free system lacking TAFIIs | Q47858026 | ||
Transcription activation in cells lacking TAFIIS. | Q48060189 | ||
A unified nomenclature for TATA box binding protein (TBP)-associated factors (TAFs) involved in RNA polymerase II transcription | Q48733526 | ||
Yeast TAFIIS in a multisubunit complex required for activated transcription. | Q52541518 | ||
TFIIA-TAF regulatory interplay: NMR evidence for overlapping binding sites on TBP. | Q52576836 | ||
Polypeptides containing highly conserved regions of transcription initiation factor σ70 exhibit specificity of binding to promoter DNA | Q54674581 | ||
Evidence for interaction of different eukaryotic transcriptional activators with distinct cellular targets | Q59098114 | ||
Function of a yeast TATA element-binding protein in a mammalian transcription system | Q59098611 | ||
Transcription factor IID mutants defective for interaction with transcription factor IIA | Q68072612 | ||
Crystal structure of the yeast TFIIA/TBP/DNA complex | Q71075240 | ||
A mechanism for TAFs in transcriptional activation: activation domain enhancement of TFIID-TFIIA--promoter DNA complex formation | Q72718834 | ||
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 | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2788-2798 | |
P577 | publication date | 2002-04-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells | |
P478 | volume | 22 |