ライフサイエンスコーパス: TATA-box binding protein

1 functionally and directly interact with the TATA box binding protein.

2 tion, and exhibited a down-regulation of the TATA box binding protein.

3 g on the bent DNA environment induced by the TATA box-binding protein.

4 at encodes an ATP-dependent inhibitor of the TATA box-binding protein.

5 iation directed by YY1 in the absence of the TATA box-binding protein.

6 ed by a polyglutamine tract expansion in the TATA box-binding protein.

7 ific interaction of double-stranded DNA with TATA box-binding protein.

8 unit 12, transcriptional coactivator CBP and TATA-box binding protein.

9 s-1, lymphoid-enhancer binding factor 1, and TATA-box binding protein.

10 tions with specific application to DNA-bound TATA-box binding protein.

11 genes are the most prominent targets of the TATA-box binding protein.

12 t with) binding of the constitutively active TATA box-binding proteins.

13 into the co-evolution hypothesis of MBF1 and TATA-box-binding proteins.

14 The tethering domain interacts with the TATA box binding protein and directs the repressor compl

15 is a multiprotein complex consisting of the TATA box binding protein and multiple tightly associated

16 TFIID comprises the TATA box-binding protein and a set of highly conserved a

17 is a multiprotein complex consisting of the TATA box-binding protein and multiple TATA box-binding p

18 DNA through interactions with promoter-bound TATA box-binding protein and transcription factor IIB.

19 r TFIID is a multisubunit complex comprising TATA-box binding protein and associated factors (TAFIIs)

20 This "mini-TFIIA" interacts with the TATA-box binding protein and can overcome repression of

21 TFIIA interacts with the TATA-box binding protein and can overcome repression of

22 to provide key insights in two examples: the TATA-box binding protein and glutamate dehydrogenase fam

23 archaeal general transcription factors, TBP (TATA-box binding protein) and TFB (archaeal homologue of

24 y with the general transcription factor TBP (TATA-box binding protein), and these two factors bind co

25 Yeast TFIID is composed of TBP, the TATA box binding protein, and 14 distinct TBP-associated

26 retention of the NF-kappaB subunit p65, the TATA box binding protein, and RNA polymerase II-essentia

27 Specifically the altered specificity TBP (TATA box binding protein) assay has been used to analyze

28 In yeast, TATA box binding protein associated factors (TAF(II)s) a

29 Here, we demonstrate that TATA-Box Binding Protein Associated Factor 1 (TAF1) asso

30 TATA-box binding protein associated factor 2 (TAF2), a c

31 ons with the glutamine-rich Q1 domain of the TATA-box binding protein associated factor 4 (TAF4) subu

32 between HCMVpp65(422-439) and TAF9(134-144) (TATA-box binding protein associated factor 9, TAF9) was

33 TATA-box binding protein associated factors (TAFs) facil

34 Serial first [TATA box binding protein-associated factor (TBP)] and th

35 ractors identified the PHD finger of TAF3, a TATA box binding protein-associated factor with importan

36 actor kinase that is most closely related to TATA box binding protein-associated factor, 250 kDa (TAF

37 her protein complexes, including a subset of TATA box binding protein-associated factors (TAFIIs) and

38 HD finger (BRPF) family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF

39 ion of TFIID in a simple system, we depleted TATA box-binding protein-associated factor (TAF)1 from D

40 nsus recognition element for the human TFIID TATA box-binding protein-associated factor TAFII31 and c

41 ne of its targets, hTAF(II)31 (a human TFIID TATA box-binding protein-associated factor).

42 its target protein, hTAFII31 (a human TFIID TATA box-binding protein-associated factor).

43 A complex of two TFIID TATA box-binding protein-associated factors (TA FIIs) is

44 of the TATA box-binding protein and multiple TATA box-binding protein-associated factors (TAF(II)s).

45 The TATA box-binding protein-associated factors (TAFs) are t

46 tial functional redundancy between TRAPs and TATA box-binding protein-associated factors in TFIID.

47 ent of activation by TR does not require the TATA box-binding protein-associated factors of TFIID.

48 are either independent or dependent on TAFs (TATA-box Binding Protein-Associated Factors).

49 These findings demonstrate how mutant TATA box-binding protein at the endogenous level affects

50 be overcome by cooperative interactions with TATA-box-binding protein at a U6 promoter but not at a U

51 Mutant TATA box-binding protein binds more tightly to the trans

52 hat are physically and genetically linked to TATA box-binding protein can provide an explanation for

53 Neuronal expression of mutant TATA box-binding protein causes age-dependent neurologic

54 complex intermediate consisting of TBP, the TATA box-binding protein component of TFIID and TFIID, v

55 However, UBF recruits the pol I-specific, TATA box-binding protein containing complex SL1 and pol

56 e proximal sequence element, which binds the TATA box-binding protein-containing complex SNAPc.

57 In solution, the TATA box binding protein from S. cerevisiae (yTBP) is on

58 The interaction of the TATA-box binding protein from the thermophilic and halop

59 model that expresses one copy of the mutant TATA box-binding protein gene, which encodes a 105-gluta

60 nalysis of the heat-shock gene hsp82 and the TATA-box-binding protein gene tbp in multiple bdelloid s

61 nscription presumably by preventing archaeal TATA-box binding protein, general transcription factor T

62 Surfaces of human TATA box-binding protein (hsTBP) required for activated

63 ption when working alone (i.e., that bearing TATA box-binding protein) is strongly influenced by prom

64 TBP (TATA-box binding protein) is a central transcription fac

65 fied a low-frequency stop-gained mutation in TATA-box binding protein-like 2 (TBPL2; c.895A>T [p.Arg2

66 Interestingly, TATA box-binding protein occupancy was greater at Pol II

67 f protein-protein interactions with TBP, the TATA box-binding protein of TFIID, and TEF-1, an enhance

68 in Acanthamoeba castellanii is regulated by TATA box binding protein promoter binding factor (TPBF),

69 The transcription activator TATA box-binding protein promoter-binding factor (TPBF)

70 Here we show that TBP (TATA box-binding protein)-related factor TRF2, but not T

71 approach and identified the Drosophila TBP (TATA-box-binding protein)-related factor 2 (TRF2) as an

72 biochemistry, and genetics to show that TBP (TATA-box-binding protein)-related factor 2 (TRF2) select

73 t of proteins (e.g alpha-synuclein, insulin, TATA-box binding protein, Sup35, p53), independent of th

74 The TATA box binding protein TBP is highly conserved and the

75 The TATA box binding protein TBP plays a universally importa

76 Interaction between the TATA box-binding protein TBP and TFIIB is critical for t

77 homologs for two of the TFIIIB subunits, the TATA box-binding protein TBP and the TFIIB-related facto

78 ranscription factor TFIID is composed of the TATA box binding protein (TBP) and a set of conserved TB

79 s is TFIID, a 700-kD complex composed of the TATA box binding protein (TBP) and a set of phylogenetic

80 lyamides inhibit the DNA binding activity of TATA box binding protein (TBP) and basal transcription b

81 III (Pol III) transcription factor (TFIIIB); TATA box binding protein (TBP) and Brf1 are the other su

82 tion factor IIIB (TFIIIB) is composed of the TATA box binding protein (TBP) and class III gene-specif

83 The transcription factor TFIID contains the TATA box binding protein (TBP) and multiple TBP-associat

84 ranscription factor TFIID is composed of the TATA box binding protein (TBP) and multiple TBP-associat

85 n of histone H3 at Lys-4, and recruitment of TATA box binding protein (TBP) and RNA polymerase II, bu

86 arge multiprotein complex is composed of the TATA box binding protein (TBP) and several TBP-associate

87 ce that inducibly express one copy of mutant TATA box binding protein (TBP) at different ages by tamo

88 esses trpEGCFBAD transcription by preventing TATA box binding protein (TBP) binding to the TATA box s

89 form of DNA observed in the complex with the TATA box binding protein (TBP) could be completed by mod

90 activating protein complex (SNAP(c)) and the TATA box binding protein (TBP) for basal transcription,

91 rity of primary and secondary structure, the TATA box binding protein (TBP) from Pw binds thermodynam

92 the thermodynamics of the interaction of the TATA box binding protein (TBP) from Pyrococcus woesei (P

93 Transcription of the TATA box binding protein (TBP) gene in Acanthamoeba cast

94 agments ( approximately 160 bp) bound by the TATA box binding protein (TBP) have demonstrated the for

95 The TATA box binding protein (TBP) is a central component of

96 The TATA box binding protein (TBP) is the platform for assem

97 ating nucleosomal histones and by recruiting TATA box binding protein (TBP) to DNA.

98 Previous work has shown that binding of the TATA box binding protein (TBP) to the TATA box is a rate

99 lex (PIC) primarily through contact with the TATA box binding protein (TBP), an interaction mediated

100 ry complex of Negative Cofactor 2 (NC2), the TATA box binding protein (TBP), and DNA has been determi

101 ive target, the general transcription factor TATA box binding protein (TBP), and the biological relev

102 Rb binds and represses Brf-1 and TATA box binding protein (TBP), subunits of RNA pol III-

103 study, 14-3-3 proteins are shown to bind the TATA box binding protein (TBP), transcription factor IIB

104 etail the interactions of initiation factors TATA box binding protein (TBP), transcription factor IIB

105 Here we report the cloning of human TATA box binding protein (TBP)-associated factor 20 (TAF

106 We demonstrate that the TATA box binding protein (TBP)-containing component of X

107 eral negative regulators which interact with TATA box binding protein (TBP).

108 rs, both through direct interaction with the TATA box binding protein (TBP).

109 rations of SNAPc contain variable amounts of TATA box binding protein (TBP).

110 iated via an interaction between p53 and the TATA box binding protein (TBP).

111 RT), and binding domains for USF, TFIIB, and TATA box binding protein (TBP).

112 eneral transcription machinery proteins, the TATA box binding protein (TBP).

113 The TATA box is recognized by TATA box binding protein (TBP).

114 tion factor D (TFIID) complex is composed of TATA box-binding protein (TBP) and 13 TBP-associated fac

115 oter depends on a TATA box that recruits the TATA box-binding protein (TBP) and a proximal sequence e

116 r TFIID is a multisubunit complex comprising TATA box-binding protein (TBP) and associated factors (T

117 n initiation factor TFIID, consisting of the TATA box-binding protein (TBP) and many TBP-associated f

118 is a multimeric protein complex composed of TATA box-binding protein (TBP) and many TBP-associated f

119 ID is a multiprotein complex composed of the TATA box-binding protein (TBP) and multiple TBP-associat

120 se I, and chemical cross-linking assays with TATA box-binding protein (TBP) and Rep68 indicate that b

121 The TATA box-binding protein (TBP) and TBP-associated factor

122 which are bound by the transcription factors TATA box-binding protein (TBP) and TFB.

123 How TATA box-binding protein (TBP) and the TBP-associated fa

124 Taken together with its binding to TATA box-binding protein (TBP) and transcription factor

125 pha DNA-binding domain binds directly to the TATA box-binding protein (TBP) and, through this interac

126 In addition, c-Rel and TATA box-binding protein (TBP) appeared to occupy the pr

127 found to be dependent not upon the canonical TATA box-binding protein (TBP) but instead upon the TBP-

128 nt regulator of basal transcription, removes TATA box-binding protein (TBP) from TATA sites in vitro.

129 box significantly reduced the recruitment of TATA box-binding protein (TBP) in the adult cells, but n

130 vating function in vivo and interaction with TATA box-binding protein (TBP) in vitro.

131 Here, we show that the TATA box-binding protein (TBP) interacts with the Cnd2 k

132 The TATA box-binding protein (TBP) is an essential component

133 The TATA box-binding protein (TBP) is highly conserved throu

134 The TATA box-binding protein (TBP) is required by all three

135 The TATA box-binding protein (TBP) plays an essential role i

136 Cocrystal structures of wild-type TATA box-binding protein (TBP) recognizing 10 naturally

137 n spatial architecture and without affecting TATA box-binding protein (TBP) recruitment.

138 e components of selective recognition of the TATA box-binding protein (TBP) to a TATA box sequence th

139 Fusing the TATA box-binding protein (TBP) to other DNA-binding doma

140 The recruitment of the TATA box-binding protein (TBP) to promoters in vivo is o

141 The recruitment of TATA box-binding protein (TBP) to promoters is one of th

142 TATA box-binding protein (TBP) was not detectable in the

143 ssays that binding interactions of the human TATA box-binding protein (TBP) were disrupted on 2-chlor

144 or early growth response factor-1 (EGR1) and TATA box-binding protein (TBP) were identified on the he

145 30) interacts with the DNA binding domain of TATA box-binding protein (TBP) which exists in the same

146 Interaction of the TATA box-binding protein (TBP) with promoters of RNA pol

147 the adjacent subunit Spt8 interact with the TATA box-binding protein (TBP)(2,7,15-17).

148 It consists of three subunits: the TATA box-binding protein (TBP), a TFIIB-related factor,

149 s of the RNA polymerase (I, II, or III), the TATA box-binding protein (TBP), and transcription factor

150 and PACAP reduce the phosphorylation of the TATA box-binding protein (TBP), resulting in a reduction

151 en shown previously that ICP4 interacts with TATA box-binding protein (TBP), TFIIB, and the TBP-assoc

152 n complex (OC) composed of the promoter DNA, TATA box-binding protein (TBP), transcription factor B (

153 -initiation complex containing promoter DNA, TATA box-binding protein (TBP), transcription factor TFI

154 nd IIA (TFIIA) to promoter DNA and induces a TATA box-binding protein (TBP)-associated factor-depende

155 TATA box-binding protein (TBP)-associated factors (TAFs)

156 endent transcription in vivo and dissociates TATA box-binding protein (TBP)-DNA complexes in vitro.

157 eraction with both the polymerase and with a TATA box-binding protein (TBP)-promoter DNA complex orie

158 upon the TATA box DNA binding properties of TATA box-binding protein (TBP).

159 for a requirement for cognate binding of the TATA box-binding protein (TBP).

160 iption factor IID components hTAF(II)130 and TATA box-binding protein (TBP).

161 ied to TATA box DNA and its complex with the TATA box-binding protein (TBP).

162 ular cofactors, including p300, pRb, and the TATA box-binding protein (TBP).

163 moter, a process which is independent of the TATA box-binding protein (TBP).

164 ed by polyglutamine (polyQ) expansion in the TATA box-binding protein (TBP).

165 rotein and mRNA of TFIIIB subunits, Brf1 and TATA box-binding protein (TBP).

166 assays revealed that the IR2P interacts with TATA box-binding protein (TBP).

167 nits contribute to overall functions of this TATA box-binding protein (TBP)/TBP-associated factor (TA

168 t1 (modifier of transcription 1) dissociates TATA box-binding protein (TBP):DNA complexes, offering a

169 ly of a preinitiation complex containing the TATA- box binding protein (TBP), transcription factor B

170 TATA-box binding protein (TBP) (but not transcription fa

171 der these experimental conditions identified TATA-Box Binding Protein (TBP) and Importin 8 (IPO8) to

172 Repressors compete with archaeal TATA-box binding protein (TBP) and TFB for the TATA-box

173 to correlate with IEP86 binding to both the TATA-box binding protein (TBP) and the transcription fac

174 of the polyglutamine (polyQ) tract in human TATA-box binding protein (TBP) causes the neurodegenerat

175 lyzes the three-dimensional structure of the TATA-box binding protein (TBP) from the hyperthermophili

176 TATA-box binding protein (TBP) is an essential factor th

177 Decades of research have shown that the TATA-box binding protein (TBP) is essential for Pol II l

178 The TATA-box binding protein (TBP) is required by eukaryotic

179 TATA-box binding protein (TBP) is required for every sin

180 pression of the general transcription factor TATA-box binding protein (TBP) leads to increased RNA sy

181 The TATA-box Binding Protein (TBP) plays a central role in r

182 Regions on the surface of human TATA-box binding protein (TBP) required for activated tr

183 ole of SAGA components in the recruitment of TATA-box binding protein (TBP) to SAGA-dependent promote

184 ), which is nucleated through binding of the TATA-box binding protein (TBP) to the promoter.

185 A unique common factor, the TATA-box binding protein (TBP), is thought to serve as a

186 TA element transcriptional regulator and the TATA-box binding protein (TBP).

187 d steps in crystal complexes of DNA with the TATA-box binding protein (TBP).

188 activating protein complex (SNAP(c)) and the TATA-box binding protein (TBP).

189 ranscription factor TFIID is composed of the TATA-box-binding protein (TBP) and a set of TBP-associat

190 ral transcription factor TFIID comprises the TATA-box-binding protein (TBP) and approximately 14 TBP-

191 0 (Rplp0), non-POU domain containing (Nono), TATA-box-binding protein (Tbp) and eukaryotic translatio

192 tiation complex, the interaction between the TATA-box-binding protein (TBP) and its binding site, the

193 iption initiation factor TFIIIB contains the TATA-box-binding protein (TBP) and polymerase III-specif

194 or 1, a multisubunit complex composed of the TATA-box-binding protein (TBP) and three TBP-associated

195 Here we consider the concept of TATA-box-binding protein (TBP) family proteins as "syste

196 The TATA-box-binding protein (TBP) homolog from Giardia inte

197 TATA-box-binding protein (TBP) is a highly conserved RNA

198 hin SPT3, a protein which interacts with the TATA-box-binding protein (TBP), suggesting that RSP5 and

199 l transcription factor complex formed by the TATA-box-binding protein (TBP), the transcription factor

200 Drosophila TATA-box-binding protein (TBP)-related factor 2 (TRF2) i

201 TATA-box-binding protein (TBP)-related factor 3, TRF3 (a

202 he basal transcription factors TFIIF and the TATA-box-binding protein (TBP).

203 romoters by mimicking and replacing cellular TATA-box-binding protein (TBP).

204 expanded polyglutamine (polyQ) repeat in the TATA-box-binding protein (TBP).

205 Here we analyse TATA-box-binding-protein (TBP) occupancy of 30 yeast pro

206 190 kDa, as well as variable amounts of the TATA box binding protein, TBP.

207 SNAP(c), and a TATA box, which recruits the TATA box-binding protein, TBP.

208 both the ubiquitous coactivator CBP and the TATA box-binding protein, TBP.

209 sal transcription factor TFIID comprises the TATA-box-binding protein, TBP, and associated factors, t

210 omoters, is made up of three components: the TATA box-binding protein, the TFIIB-related Brf, and the

211 polymerase II (RNAPII), enhanced binding of TATA box-binding protein to RNAPII and selectively promo

212 rotein-protein interactions involving Pax-6, TATA-box-binding protein (TPB), and retinoblastoma prote

213 -initiation complex by M. thermautotrophicus TATA-box-binding protein, transcription factor B, and RN

214 The 27-kDa subunit of TFIIIB or the TATA box binding protein was photoaffinity labeled at bp

215 NA binding of TFIIIB subunits, Brf1 and TBP (TATA-box binding protein), which results in the full-len

216 vage agent to specific residues in the yeast TATA box binding protein (yTBP), we demonstrate that, in