ライフサイエンスコーパス: binding sequence

1 bunit alpha, to the sGCbeta1 promoter (CCAAT binding sequence).

2 hering of proteins through an engineered CaM-binding sequence.

3 ys to alternative modifications within their binding sequence.

4 iption factor NF-kappaB with its cognate DNA binding sequence.

5 ied BaMV RNA containing the MS2 coat protein binding sequence.

6 id C-terminus that matches an NRP1 consensus binding sequence.

7 g SAM (OFF state) by encrypting the ribosome binding sequence.

8 rial oriCs generally differ from the optimal binding sequence.

9 n extracted an optimal palindromic 13 bp DSX-binding sequence.

10 son to a functionally derived consensus BvgA-binding sequence.

11 interacts with caveolin-1 via its caveolin-1-binding sequence.

12 n function in the absence of its cognate DNA-binding sequence.

13 PDZ-RhoGEF and frabin identify a novel actin-binding sequence.

14 y as a fail-safe measure to ensure a correct binding sequence.

15 of a cytosine residue flanking the core CSL binding sequence.

16 ds Rps23, Nro1, and Sre1 through a consensus binding sequence.

17 of an oligonucleotide encompassing the CrgA-binding sequence.

18 the Pbx1 promoter segment harboring the CSL-binding sequence.

19 SP, which is similar to the consensus 14-3-3 binding sequence.

20 cific enhancers that lack the consensus MEF2-binding sequence.

21 in p53beta mRNA through the consensus SRSF3-binding sequences.

22 signature sequence, and FAD-binding and NADP-binding sequences.

23 us 8 E2, and prototype foamy virus chromatin-binding sequences.

24 ucts bearing the En1/2 and Lmx1a 3'UTR miRNA-binding sequences.

25 highlighted by the presence of ETS- and AP-1-binding sequences.

26 d weight matrices were built to model SyCrp1 binding sequences.

27 ne for the introduction of discrete integrin-binding sequences.

28 ssociation with evolutionarily conserved Otd-binding sequences.

29 nto CLADE, resulting in some of the tightest binding sequences.

30 th expression of microRNAs targeting triplex binding sequences.

31 ed by other, heterologous phosphatidylserine-binding sequences.

32 20 natural amino acids and identified novel binding sequences.

33 logous to known carbonic anhydrase II (CAII) binding sequences.

34 Pax6-PD, Pax6-PD/HD and Pax6-HD established binding sequences.

35 rve enrichment of the canonical T-domain DNA binding sequence 5'-TCACACCT-3' in the vicinity of most

36 Mutations at the CCAAT binding sequence, a major element regulating sGCbeta1 ex

37 vivo approach, we show that removing the VCP-binding sequence abolishes axon protection.

38 Mutation of the mouse or human GATA binding sequence abrogates binding of TRPS1 to the osteo

39 A synthetic actin-binding sequence (ABS) peptide 326 with amino acid seque

40 The HPV8 E2 chromosome binding sequence also has sequence similarity with chrom

41 6 is contained within a predicted calmodulin-binding sequence and acetylation of Lys-306 strongly inh

42 leotide that contains a transcription-factor-binding sequence and hydrophobic membrane-disruptive cha

43 de at each position in the consensus p53 DNA binding sequence and identified substitutions tolerated

44 phatase activity, its extreme C-terminal PDZ binding sequence and probably Myosin 5A to control lumen

45 rent levels of RfaH by altering the ribosome-binding sequence and start codon.

46 ng sites, suggest how the ordered nucleotide binding sequence and structural changes are dynamically

47 assays validated the identity of the APUM23 binding sequence and supported the location of 3 of the

48 f the tail - the ATP-independent microtubule-binding sequence and the IAK autoinhibitory motif - are

49 f the modification in terminating the primer-binding sequence and thus limiting run-on transcription,

50 5 occupy enhancers that are enriched for ETS-binding sequences and are both functionally important fo

51 By site-directed mutagenesis of SR34 RNA-binding sequences and Arg/Ser-rich (RS) domain, we furth

52 coding PalmtdTomato were tagged with MS2 RNA binding sequences and detected by co-expression of bacte

53 ch revealed enrichment for androgen receptor binding sequences and hypomethylation of these segments

54 d greatly expand the repertoire of HNF4alpha-binding sequences and target genes, thereby identifying

55 TP0262 specifically recognizes the putative binding sequences and that DNA binding is cAMP-dependent

56 We identified approximately 1400 new binding sequences and used this dataset to successfully

57 of RelA, its association to a DNA consensus binding sequence, and NF-kappaB transcriptional activity

58 pastin also displays an adjacent microtubule binding sequence, and the presence of both ESCRT-III and

59 vivo peak in DSX binding and an optimal DSX-binding sequence, and thus are almost certainly direct D

60 BEND to design both strong and weak histone- binding sequences, and measured the corresponding free e

61 s corresponding to predicted GroEL consensus binding sequences, and that the structure of the bound p

62 e for the introduction of mammalian integrin-binding sequences, and these sequences may be manipulate

63 endogenous Gag polyproteins sharing the same binding sequence; and several proteins involved in cytos

64 Additionally, we identified a conserved Fur binding sequence approximately 130 bp upstream of the tr

65 or double mismatches to the Py-Im polyamide binding sequence are not enriched.

66 h position in the required (Gly-Xaa-Yaa)6 Fn-binding sequence are probed here, using model peptides a

67 Binding sequences are amplified by PCR using fluorescein

68 ETS/AP-1-binding sequences are prototypical RAS-responsive elemen

69 osphorylated protein containing the integrin binding sequence Arg-Gly-Asp through which it interacts

70 Our method represents DNA binding sequences as a hidden Markov model which capture

71 olar cells and interacted with the predicted binding sequences as assessed by electrophoretic mobilit

72 nspired polypeptides with low-complexity RNA-binding sequences as well as an archetypal disordered RN

73 ter revealed the presence of 1 putative STAT-binding sequence at -476 nt, and electrophoretic mobilit

74 Instead, a putative SRSF1 binding sequence at the 3' end of exon 2 directs CD33 ex

75 ry miRNA transcripts and identified the ICP4-binding sequences at the transcription initiation sites

76 tides that are methylated in their consensus binding sequence, both in in vitro biochemical binding a

77 region, both of which contained multiple Sp1-binding sequences but lacked classic progesterone respon

78 the ability of a peptide with perturbed PDZ-binding sequence, but preserved CaMKIIalpha binding (TAT

79 nd entropic contributions, as expected for a binding sequence, but that D2 gives rise to entropic pen

80 human E2F1 promoter, which lacks a LANA DNA-binding sequence, but this function requires both the N

81 analyses identified putative PLZF and SALL4 binding sequences, but rarely both at shared sites, indi

82 The introduction of STAT3 DNA-binding sequences by site-specific mutagenesis in an imm

83 showed that mutations (GT-->TG) in the Reb1p-binding sequence caused an 8.6-fold reduction in beta-ga

84 associates with chromosomes via a chromatin-binding sequence (CBS) located within its C-terminal reg

85 idermal growth factor-like domain and a uPAR-binding sequence comparable with that found in mammalian

86 unique 93 base pair (bp)-long (+/-2 bp) ArgR-binding sequence containing two ARG boxes (39 bp) and re

87 nsitivity resulting from mutations in the Fn-binding sequence could lead to degradation of type I col

88 rofiles, genome-wide location analysis data, binding sequence data, and gene ontology (GO) informatio

89 xpression of the genes containing a RORE DNA binding sequence (DBS), including the Bmal1 gene, thereb

90 also nearly identical to the consensus KLF11 binding sequence defined here by random oligonucleotide

91 .5F proteins containing a scrambled integrin-binding sequence, demonstrating the importance of target

92 The specific GR binding sequence did not impact sensitivity, and we inst

93 ical, and cell-based assays, we show that GR binding sequences, differing by as little as a single ba

94 the CjFur crystal structure rationalize the binding sequence diversity that was uncovered during ChI

95 nosine-5'-triphosphate (ATP) aptamer) or ion-binding sequences (e.g., T-rich Hg(2+) ion-binding domai

96 and Syk, we examined the role of PSGL-1 ERM-binding sequence (EBS) on cell capture, rolling, and sig

97 erts its function on Capsella fruit shape by binding sequence elements of auxin biosynthesis genes to

98 Site-directed mutagenesis of the NKX6.1 core-binding sequence eliminated NKX6.1-mediated activation a

99 s onto SiO2 particles mediated by the silica-binding sequence enables visual detection of environment

100 e-engineering reporter plasmids with shuttle binding sequences enhances gene transfer.

101 variants that reside on transcription-factor-binding sequences fall in STF target sequences, suggesti

102 produced a shared dataset of FMRP consensus binding sequences (FCBS), which were reproducibly identi

103 lection to selectively enrich cross-reactive binding sequences, followed by serial selection that enr

104 We report the identification of a novel RNA binding sequence for a nucleolar Arabidopsis PUF protein

105 in depolymerizing factor, which has a common binding sequence for actin and PIP(2), was required for

106 e we report the identification of an optimal binding sequence for BEN by SELEX (systematic evolution

107 ed a constitutive SFFV promoter and NFkappaB binding sequence for bioluminescence and biosensor evalu

108 We determined the consensus binding sequence for BNC2 in vitro, verified its enrichm

109 l peptide library, we identified a consensus binding sequence for each PDZ domain.

110 partate (RGD)-containing sequence (consensus binding sequence for integrins) allowed us to detect a s

111 gh Mg(2+), subsequently opening the ribosome-binding sequence for mgtL translation.

112 Moreover, the -254(C-->G) SNP creates a binding sequence for nuclear factor-kappaB.

113 The consensus DNA binding sequence for PrrA, a global regulator in Rhodoba

114 The polymorphism is located in a consensus binding sequence for the E2F family of transcription fac

115 a putative Na3 site and propose a plausible binding sequence for the substrate and the three Na(+) i

116 The binding sequence for the three substrates has been debat

117 h an miR-155 retrovirus identified potential binding sequences for BACH1 and ZIC3.

118 However, the LIMP-2/SCARB2 binding sequences for enterovirus 71 and GCase are not s

119 NFAIP2, we were unable to correlate specific binding sequences for GR or occupancy patterns with repr

120 ing region of H2a mRNA harbors high affinity binding sequences for Lin28 and that these sequences sti

121 Most gene promoters have multiple binding sequences for many transcription factors, but th

122 odimer binds to a specific DRE that overlaps binding sequences for peroxisome proliferator-activated

123 protein structures, thermodynamic data, and binding sequences for the corresponding transcription fa

124 with a PPT model computed from high affinity binding sequences for U2AF65.

125 ike superfamily of periplasmic peptidoglycan-binding sequences, found in several types of bacterial m

126 AP-ADAP chimera contains the CARMA1 and TAK1 binding sequences from ADAP, expression of the chimera d

127 A search with known CSL binding sequences from cellular genes found at least 260

128 n vivo screen allows the mapping of putative binding sequences from hundreds of proteins simultaneous

129 the drug on a monolithic column to partition binding sequences from nonbinding sequences using a low-

130 Comparison of the AmpR-binding sequences from the transcriptome and ChIP-Seq an

131 transiently transfected with pDNA containing binding sequences from two of the DNA shuttle proteins,

132 However, increased expression of p53-binding sequences from uPA, uPAR, and PAI-1 mRNA 3' untr

133 p53-binding sequences from uPA, uPAR, and PAI-1 mRNA 3' untr

134 TREs via sequence-specific contacts to a GR-binding sequence (GBS) half-site found embedded within t

135 We predicted a novel and selective integrin-binding sequence, GFPGEN, through the use of computer mo

136 f MTM recognition of DNA, including the FLI1 binding sequence GGA(A/T), are needed to understand how

137 s containing a putative transcription factor binding sequence, GGAANCGGAANY, and a nucleolar gene net

138 ntify a conserved Bub3 interacting and GLE-2-binding sequence (GLEBS) containing ZNF207 (BuGZ) that a

139 and mitosis through a highly conserved GLE2p-binding sequence (GLEBS) domain.

140 cture of human Rae1 in complex with the Gle2-binding sequence (GLEBS) of Nup98 at 1.65 A resolution.

141 lis2 binds effectively to the consensus Glis binding sequence (GlisBS) (G/C)TGGGGGGT(A/C).

142 f a single terminal nucleotide in one of the binding sequences had little effect on the efficiency of

143 Furthermore, a potential cholesterol-binding sequence has also been predicted in the p24 tran

144 High affinity VWF-binding sequences have been identified in the homotrimer

145 t NTD, or a peptide of the TSP1 calreticulin-binding sequence (hep I) increased both collagen express

146 oxygen-terminated side the consensus peptide-binding sequence (HSXXH) was predicted in silico and con

147 tion of nanocrystal mineralizers through ZnS binding sequences identified by cell surface display and

148 Removal of the CaM-binding sequence in AKAP79 prevents formation of a Ca(2+

149 Significantly, disruption of the Pumilio-binding sequence in chemotaxis pathway mRNAs, or misloca

150 Finally, the CTCF-binding sequence in CMV is evolutionarily conserved, as

151 These results define a novel actin-binding sequence in PDZ-RhoGEF with a critical amino aci

152 C1b region of AC-AplA that resembles the CaM-binding sequence in the C1b region of AC1 in mammals.

153 ent on a myocyte enhancing factor-2A (MEF2A)-binding sequence in the core KLF2 promoter.

154 opts a phosphatidylinositol 4,5-bisphosphate-binding sequence in the cytoskeletal protein gelsolin.

155 Here, we identify a novel p53-binding sequence in the distal human SIRT1 promoter that

156 re we report the identification of the ATG12 binding sequence in the flexible region of human ATG3 an

157 Thus, a common SNP in a novel p53-binding sequence in the human SIRT1 promoter affects nut

158 ciation between ARID3B and a specific ARID3B-binding sequence in the Oct4 promoter.

159 TRPS1 binds through a GATA binding sequence in the proximal promoter of the osteoca

160 We found a let-7d binding sequence in the tlx 3' UTR and demonstrated that

161 ranscription factors find their specific DNA binding sequence in the vast expanse of the cell and how

162 e significance of degeneracy within the PpsR binding sequence in vivo, we adapted the chromatin immun

163 B, which now contains almost 15 million CTCF-binding sequences in 10 species.

164 of cycB in immature spermatocytes, with Rbp4 binding sequences in a cell type-specific shortened form

165 anner, and the distance between the two BlcR-binding sequences in DNA was critical for BlcR-DNA assoc

166 affected by the distance separating the BlcR-binding sequences in DNA.

167 the other one (Cdc20(A)) through additional binding sequences in Mad3/BubR1 [4-6].

168 introduce a new algorithm to identify Hsp70 binding sequences in proteins-ChaperISM-a position-indep

169 ty to differentially bind to highly variable binding sequences in target proteins.

170 the role of the spatial organization of H-NS-binding sequences in the assembly of long-range nucleopr

171 Here, we mutated the SaeR-binding sequences in the hla regulatory region and deter

172 under physiologic conditions with degenerate binding sequences in the presence of other biologically

173 ences that are similar to mitotic chromosome-binding sequences in the transcriptional pioneer protein

174 ides corresponding to naturally occurring Zn-binding sequences in transcription factors have been qua

175 ulfate, and the presence of a NRP1 consensus binding sequence indicate that NRP1 is the binding site

176 neurin ICDs do not contain any intrinsic DNA binding sequences, interaction partners are required to

177 fficient pentamer algorithm by splitting DNA binding sequences into overlapping fragments along with

178 cAMP-response element-binding protein (CREB) binding sequence is present in the Ape1 gene (encodes AP

179 A DNA binding sequence is split into overlapping pentamers (5

180 While the number of material-binding sequences is large, at present, quantitative mat

181 in consequence, the landscape of functional binding sequences is sparse but robust, favoring scenari

182 A conserved NF-kappaB-binding sequence (kappaB-site) was identified in the pro

183 Interestingly, the consensus Nedd8 binding sequence, L(X7)R(X5)F(X)ALQ is conserved in both

184 ibition of NFkappaB interacting with its DNA binding sequences, leading to decreased expression of NF

185 Gly replacements at four sites within the Fn-binding sequence led to decreased Fn binding to denature

186 The p53-binding sequence lies in a region of the SIRT1 promoter

187 Here, we identify a cluster of three binding sequences located downstream of IR exon 11 that

188 plex with the neuronal nitric oxide synthase binding sequence), Lys-148 at the C-terminus of CaM form

189 een BubR1 and Bub3, for which the BubR1 Gle2 binding sequence motif is essential.

190 This novel AR-binding sequence motif is found in regions predicted to

191 r was demonstrated, and transcription factor-binding sequence motifs were identified.

192 ctin nucleation activity via a cryptic actin-binding sequence near JMY's N terminus, and STRAP inhibi

193 ration of decoy ODNs comprising the NRSF DNA-binding sequence (neuron restrictive silencer element [N

194 s of hPDI are that it contains consensus DNA-binding sequences not only for nearly 500 human transcri

195 a plasmid encoding the secreted calreticulin-binding sequence [NTD (1-35)-EGFP] or a control sequence

196 ent with a peptide derived from the Galpha13-binding sequence of beta1 abolished Galpha13-beta1 inter

197 r by T1 peptide (derived from an alpha6beta1-binding sequence of CCN1) disrupted the positive-feedbac

198 domain and the PSD-95/Discs-large/ZO-1 (PDZ)-binding sequence of DAT, was made membrane-permeable by

199 hemic injury in vivo The minimal syntaxin 1A-binding sequence of Kv2.1 C terminus (C1aB) was first id

200 to neurexins, and mutation of the PDZ-domain binding sequence of neurexin-3beta blocked its transport

201 We have determined the preferred DNA binding sequence of Opa by SELEX and shown that it is ne

202 ntrast, the conserved putative synaptotagmin-binding sequence of SV2 is fully dispensable.

203 develop and validate aptamers containing the binding sequence of TF AP-1 (5ECdsAP1), in order to eluc

204 A synthetic peptide that mimics the main FN-binding sequence of TG2 blocks the formation of TG2-FN c

205 ription factor 1 (MyT1-2), and the second Zn-binding sequence of the DNA-binding domain of glucocorti

206 tein created by replacing a natural receptor-binding sequence of the ecotropic Moloney murine leukemi

207 reproduced with a peptide possessing a CD36 binding sequence of TSP-1, while the effects of TSP-1 we

208 n of collagen deposition by the calreticulin-binding sequence of TSP1.

209 nt within putative regulatory regions of the binding sequences of a diverse library of 104 nonredunda

210 structure of calmodulin (CaM) bound with CaM-binding sequences of either the plasma membrane Ca-ATPas

211 nding protein and bends all three tested DNA binding sequences of HMGA2, SELEX1, SELEX2, and PRDII.

212 d cell-type specific regulatory regions with binding sequences of master transcription factors involv

213 d acidic cluster motif reminiscent of ARP2/3-binding sequences of NPFs but fails to facilitate ARP2/3

214 was Ca(2+)-independent, mutations in Ca(2+)-binding sequences of synaptotagmin-1 or synaptotagmin-7-

215 eal that Oct-1 binds to the putative octamer-binding sequences of the dysregulated genes and that thi

216 tely matched both the intronic and exonic U1 binding sequences of the mutated DDC gene could correct

217 d several U1 snRNA vectors to adapt U1 snRNA binding sequences of the mutated DDC gene.

218 ely ascribed to three differences in the CaM-binding sequences of the two reporters.

219 By controlling the position of the binding sequence on a single helix that spans the hollow

220 effect of the downstream coat gene ribosome binding sequence on maturation gene expression appeared

221 98-602) clusters, forming accessible heparin binding sequences on the TG2 three-dimensional structure

222 nerated by first grafting the murine antigen binding sequences onto suitable human variable light and

223 lly in the absence of any apparent signature binding sequence or motif, remains unknown.

224 tion that maximizes the enrichment of target-binding sequences over non-target-binding (i.e., backgro

225 y base pairing occurs between the HIV primer binding sequence (PBS) and the tRNA's 3'-terminus, an im

226 ptidase activity: mutations in its ubiquitin-binding sequences positioned within the ubiquitin-specif

227 leton in TM-1 cells is the syndecan/integrin binding sequence, PPRARI.

228 h, called DeBooster, to accurately model the binding sequence preferences and identify the correspond

229 TF binding sequence preferences are conserved within family

230 2 (CCT2), which resembles the core COP1-WD40-binding sequences present in the substrates of COP1.

231 70) signatures, and deletion of the sigma(E) binding sequence prevented transcriptional activation of

232 nd that peptides containing the RGD integrin-binding sequence produce sustained vasodilatation of rat

233 ndicate that TH has a different co-substrate binding sequence (pterin + O(2) + L-tyr) than PAH (L-phe

234 mutation of a nucleotide in the middle of a binding sequence reduced both the in vitro protein bindi

235 substitutions within the C-terminal receptor-binding sequence, reduced metabolization and improved tu

236 l perturbations of the somatostatin receptor-binding sequence relative to the Re-free disulfide analo

237 of hasS or of the terminator eliminates CovR-binding sequences, relieving repression and increasing r

238 ain with an alternative ataxin-3-derived VCP-binding sequence restores its protective function.

239 -pre-mRNA interactions, based on intron-exon binding sequences, result in reduced abundance of splice

240 isrupts the mirror image symmetry of the p53-binding sequence, resulting in decreased binding to p53,

241 , we extended EKEKEKE-PPPPC-Am with the cell-binding sequence RGD and demonstrated control over speci

242 as repressing complexes to their cognate DNA-binding sequence(s) (DBS) in the TSLP promoter regulator

243 oprecipitation (ChIP), we identified 24 SlmA-binding sequences (SBSs) on the chromosome.

244 at the nonreducing end and two contiguous AT-binding sequences separated by a nonsulfated iduronate r

245 A mutational analysis of the binding sequences showed that ComE does not require both

246 y between the two ends of the 23-mer minimal binding sequence, showing an unprecedented influence of

247 Variation of the MalR binding sequence significantly reduced MalR binding in v

248 Cis-regulatory modules (CRMs) function by binding sequence specific transcription factors, but the

249 Telomeres avert the former peril by binding sequence-specific end-protection factors that co

250 anscription of ER stress response genes upon binding sequence specifically to ER stress response enha

251 protein p53 acts as a transcription factor, binding sequence-specifically to defined DNA sites, ther

252 anscription of ER stress response genes upon binding sequence-specifically to ER stress response enha

253 RNA interactions combined with a fluorophore-binding sequence 'Spinach', a GFP-like RNA aptamer for w

254 However, non-coding DNA binding sequences, such as transcription factor binding

255 in domain and significant clustering of SeqA-binding sequences, suggesting a role for SeqA in cluster

256 at CpG dinucleotides flanking the NF-kappaB-binding sequence, supporting that this active DNA demeth

257 l of which contain clusters of the consensus binding sequence TAATCC.

258 evolutionary conservation of Pitx2 consensus binding sequence, TAATCY, on the -20 kb, intronic and co

259 evolutionary conservation of Pitx2 consensus binding sequence, TAATCY, on the -20kb, intronic, and co

260 pn-2) and PlexinA3 (PlexA3) through an Npn-2-binding sequence (TARNER) in the extracellular Ig1 domai

261 pend on residues upstream from the canonical binding sequence that are likely to interact with flexib

262 urexin sequence with an unrelated PDZ-domain binding sequence that does not bind to CASK fully restor

263 aMKIIdelta 3'UTR contains a consensus miR-30 binding sequence that is highly conserved across species

264 ototypic traits of a glycosaminoglycan (GAG) binding sequence that mediates Otx2 binding to PNNs, and

265 The Ctgf promoter contained an Hnf4alpha binding sequence that overlapped with the cis-regulatory

266 selection of targets identified a DACH1 DNA-binding sequence that resembles the FOX (Forkhead box-co

267 rus LANA and prototype foamy virus chromatin-binding sequences that blocked nucleosome association fa

268 at PPE41 contains a characteristic chaperone-binding sequence, the hh motif, which is highly conserve

269 in vivo expression of the TSP1 calreticulin-binding sequence to determine the role of TSP1 in tissue

270 beta-glucosidase (glucocerbrosidase (GCase)) binding sequence to LIMP-2 (lysosomal integral membrane

271 clamp zones recruit proteins bearing a clamp-binding sequence to replication foci, the results highli

272 tion of a DNA fragment containing the kappaB binding sequence to the IkappaBalpha-NF-kappaB complex r

273 inds to promoters containing Gal4p consensus binding sequences to activate transcription.

274 to the exponential increase in the number of binding sequences to be evaluated for longer binding sit

275 ndogenous kinase substrates and known Tb(3+)-binding sequences to build a generalizable in silico pip

276 We anticipate that consensus binding sequences together with the related DNA dynamics

277 -BB) that were engineered to have a syndecan-binding sequence trigger sustained low-intensity signall

278 The N- and C-domains contain the nucleotide-binding sequences Walker A and Walker B, respectively.

279 The Arabidopsis PUM23 (APUM23) binding sequence was 10 nucleotides in length, contained

280 eptide incorporating a fibronectin II insert-binding sequence was constructed and found to selectivel

281 ntity of these residues and their target DNA-binding sequence was constructed.

282 ar single quantum coherence NMR, the optimal binding sequence was identified as TTGT.

283 An ExsA consensus binding sequence was identified upstream of the impA gen

284 ly 25 genes, and a highly conserved MalR DNA-binding sequence was identified.

285 is using promoter fusions revealed that this binding sequence was required for Fe-Fur-mediated activa

286 rotein rDA27(aa 33-84) that removes the GAGs-binding sequences was also used for comparison.

287 The elution profile of binding sequences was compared to that of a blank column

288 luronan mediated motility (RHAMM) hyaluronan binding sequences, was the most effective inhibitor.

289 tional approximately 10,000 unique HNF4alpha-binding sequences; we also identify new rules for HNF4al

290 ger deletions that extended beyond the TALEN-binding sequences were also detected and were similarly

291 ophoretic mobility shift assay, and the MisR binding sequences were mapped.

292 o acids in the alpha-helix of the calmodulin binding sequence, which disrupts kinase binding to calmo

293 Ac-d-Trp-PheNH(2) appeared to be the minimal binding sequence, while Ac-d-Trp-Phe-GlyNH(2) emerged as

294 modified GAL1 promoter containing six Zif268 binding sequences (with single nucleotide spacing) was s

295 nctional interaction of Sp1 with a consensus binding sequence within the 220-bp region.

296 anscription factor to a highly conserved p53-binding sequence within the MMP-2 promoter.

297 ion mixture is to outcompete any nonspecific binding sequences within the initial library, thus allow

298 tted across transmembrane integrins onto RGD binding sequences within the tenth FN type III (10FNIII)

299 t transfection assays, we identified TCF/LEF-binding sequences within two distal enhancers of the Irx

300 at did or did not contain the IE62 consensus binding sequence yielded K(D) (equilibrium dissociation