| Q36097406 | A common site on TBP for transcription by RNA polymerases II and III |
| Q33960174 | A human TATA binding protein-related protein with altered DNA binding specificity inhibits transcription from multiple promoters and activators |
| Q77763072 | A regulated two-step mechanism of TBP binding to DNA: a solvent-exposed surface of TBP inhibits TATA box recognition |
| Q36565816 | A severely defective TATA-binding protein-TFIIB interaction does not preclude transcriptional activation in vivo |
| Q42435929 | A shared surface of TBP directs RNA polymerase II and III transcription via association with different TFIIB family members |
| Q33292569 | Activity of the upstream TATA-less promoter of the p21(Waf1/Cip1) gene depends on transcription factor IIA (TFIIA) in addition to TFIIA-reactive TBP-like protein |
| Q34330160 | Adenovirus E1A N-terminal amino acid sequence requirements for repression of transcription in vitro and in vivo correlate with those required for E1A interference with TBP-TATA complex formation |
| Q39574684 | Architecture of protein and DNA contacts within the TFIIIB-DNA complex |
| Q33963967 | Artificial recruitment of TFIID, but not RNA polymerase II holoenzyme, activates transcription in mammalian cells |
| Q28218061 | Assembly of human small nuclear RNA gene-specific transcription factor IIIB complex de novo on and off promoter |
| Q39583813 | Association of transcription factor IIA with TATA binding protein is required for transcriptional activation of a subset of promoters and cell cycle progression in Saccharomyces cerevisiae |
| Q42693136 | BRCA1 can stimulate gene transcription by a unique mechanism |
| Q28216622 | BRFU, a TFIIB-like factor, is directly recruited to the TATA-box of polymerase III small nuclear RNA gene promoters through its interaction with TATA-binding protein |
| Q40722269 | Comparative study and identification of potent eukaryotic transcriptional repressors in gene switch systems |
| Q39445508 | Corepressor required for adenovirus E1B 55,000-molecular-weight protein repression of basal transcription |
| Q39575245 | DA-complex assembly activity required for VP16C transcriptional activation |
| Q33890400 | Destruction of Myc by ubiquitin-mediated proteolysis: cancer-associated and transforming mutations stabilize Myc. |
| Q41472140 | Elevated TATA-binding protein expression drives vascular endothelial growth factor expression in colon cancer |
| Q59098614 | Enhancement of TBP binding by activators and general transcription factors |
| Q74369894 | Eukaryotic transcription factors |
| Q30700508 | Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells |
| Q27940253 | Functional and structural organization of Brf, the TFIIB-related component of the RNA polymerase III transcription initiation complex |
| Q27936603 | Genetic analysis connects SLX5 and SLX8 to the SUMO pathway in Saccharomyces cerevisiae |
| Q39574625 | Hepatitis B virus pX targets TFIIB in transcription coactivation |
| Q24548443 | Identification of a mouse TBP-like protein (TLP) distantly related to the drosophila TBP-related factor |
| Q44562084 | Identification of a novel TATA element-binding protein binding region at the N terminus of the Saccharomyces cerevisiae TAF1 protein |
| Q39745952 | Increased expression of TATA-binding protein, the central transcription factor, can contribute to oncogenesis. |
| Q35110832 | Interaction between transactivation domain of p53 and middle part of TBP-like protein (TLP) is involved in TLP-stimulated and p53-activated transcription from the p21 upstream promoter |
| Q41577326 | Interconversion between active and inactive TATA-binding protein transcription complexes in the mouse genome |
| Q27940351 | Intermediates in formation and activity of the RNA polymerase II preinitiation complex: holoenzyme recruitment and a postrecruitment role for the TATA box and TFIIB. |
| Q28198008 | Mammalian Srb/Mediator complex is targeted by adenovirus E1A protein |
| Q94671419 | Molecular determinants underlying functional innovations of TBP and their impact on transcription initiation |
| Q29620260 | Molecular genetics of the RNA polymerase II general transcriptional machinery |
| Q40282941 | Mutational and functional analysis of an essential subdomain of the adenovirus E1A N-terminal transcription repression domain |
| Q42494682 | Mutations in the TATA-binding protein, affecting transcriptional activation, show synthetic lethality with the TAF145 gene lacking the TAF N-terminal domain in Saccharomyces cerevisiae |
| Q36959650 | Nonradioactive, ultrasensitive site-specific protein-protein photocrosslinking: interactions of alpha-helix 2 of TATA-binding protein with general transcription factor TFIIA and transcriptional repressor NC2. |
| Q40709416 | POU/TBP cooperativity: a mechanism for enhancer action from a distance |
| Q39574692 | Polymerase (Pol) III TATA box-binding protein (TBP)-associated factor Brf binds to a surface on TBP also required for activated Pol II transcription |
| Q77220172 | Promoter-specific activation defects by a novel yeast TBP mutant compromised for TFIIB interaction |
| Q45970861 | Protease footprinting analysis of ternary complex formation by human TFIIA. |
| Q35676609 | RNA aptamers directed to discrete functional sites on a single protein structural domain. |
| Q41477041 | RNA polymerase II holoenzyme and transcriptional regulation |
| Q24614755 | RNA polymerase II transcription initiation: a structural view |
| Q35898197 | Readthrough activation of early adenovirus E1b gene transcription. |
| Q34098614 | Reconfiguring the connectivity of a multiprotein complex: fusions of yeast TATA-binding protein with Brf1, and the function of transcription factor IIIB |
| Q42482323 | Role of the TATA binding protein-transcription factor IIB interaction in supporting basal and activated transcription in plant cells |
| Q37056397 | Role of the inhibitory DNA-binding surface of human TATA-binding protein in recruitment of human TFIIB family members |
| Q33774811 | Simian virus 40 large T antigen stabilizes the TATA-binding protein-TFIIA complex on the TATA element |
| Q43247301 | Site-specific cross-linking of TBP in vivo and in vitro reveals a direct functional interaction with the SAGA subunit Spt3. |
| Q40644685 | Skp2 regulates Myc protein stability and activity |
| Q42834860 | Specific interaction with transcription factor IIA and localization of the mammalian TATA-binding protein-like protein (TLP/TRF2/TLF). |
| Q24810339 | Stimulation of Myc transactivation by the TATA binding protein in promoter-reporter assays |
| Q39745923 | Structural and functional analysis of mutations along the crystallographic dimer interface of the yeast TATA binding protein |
| Q39446445 | Synergistic transcriptional activation by TATA-binding protein and hTAFII28 requires specific amino acids of the hTAFII28 histone fold |
| Q39528791 | TAF(II)170 interacts with the concave surface of TATA-binding protein to inhibit its DNA binding activity |
| Q77313418 | TATA box mimicry by TFIID: autoinhibition of pol II transcription |
| Q22009469 | TATA box-binding protein (TBP)-related factor 2 (TRF2), a third member of the TBP family |
| Q24519079 | TATA-binding protein (TBP)-like factor (TLF) is a functional regulator of transcription: reciprocal regulation of the neurofibromatosis type 1 and c-fos genes by TLF/TRF2 and TBP |
| Q33962132 | TATA-binding protein mutants that increase transcription from enhancerless and repressed promoters in vivo |
| Q46145585 | TATA-flanking sequences influence the rate and stability of TATA-binding protein and TFIIB binding |
| Q41760708 | TBP domain symmetry in basal and activated archaeal transcription |
| Q38313033 | TFIIA has activator-dependent and core promoter functions in vivo |
| Q73075615 | TFIIA regulates TBP and TFIID dimers |
| Q34350684 | The Epstein-Barr virus immediate-early protein BZLF1 regulates p53 function through multiple mechanisms |
| Q27648719 | The carboxy-terminal coiled-coil of the RNA polymerase β′-subunit is the main binding site for Gre factors |
| Q28189110 | The genetics of TBP and TBP-related factors |
| Q34137662 | The germ cell-specific transcription factor ALF. Structural properties and stabilization of the TATA-binding protein (TBP)-DNA complex |
| Q52533599 | The structure of the site on adenovirus early region 1A responsible for binding to TATA-binding protein determined by NMR spectroscopy. |
| Q39597497 | The transcriptional co-activator P/CAF potentiates TGF-beta/Smad signaling |
| Q40442512 | The zinc ribbon domains of the general transcription factors TFIIB and Brf: conserved functional surfaces but different roles in transcription initiation. |
| Q41720781 | Transcription: TRF walks the walk but can it talk the talk? |
| Q36573748 | Transcriptional activation by TFIIB mutants that are severely impaired in interaction with promoter DNA and acidic activation domains |
| Q35058517 | Transcriptional activation by artificial recruitment in mammalian cells |
| Q34608335 | Transcriptional activation in yeast cells lacking transcription factor IIA. |
| Q39747839 | Vertebrate TBP-like protein (TLP/TRF2/TLF) stimulates TATA-less terminal deoxynucleotidyl transferase promoters in a transient reporter assay, and TFIIA-binding capacity of TLP is required for this function |
| Q39758897 | p53 represses RNA polymerase III transcription by targeting TBP and inhibiting promoter occupancy by TFIIIB. |
| Q35196731 | pX, the HBV-encoded coactivator, suppresses the phenotypes of TBP and TAFII250 mutants |