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

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

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

5 rial oriCs generally differ from the optimal binding sequence.

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

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

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

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

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

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

12 of an oligonucleotide encompassing the CrgA-binding sequence.

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

14 en in the absence of an operational clathrin binding sequence.

15 a p190B mutant specifically lacking the Rac1-binding sequence.

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

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

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

19 ys to alternative modifications within their binding sequence.

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

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

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 weak (K(d)>1 mM) and tight (K(d)<10 microM) binding sequences.

31 quence compared with other characterized LC8 binding sequences.

32 thesis gene cluster and have degenerate PpsR binding sequences.

33 th expression of microRNAs targeting triplex binding sequences.

34 ed by other, heterologous phosphatidylserine-binding sequences.

35 20 natural amino acids and identified novel binding sequences.

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

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

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

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

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

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

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

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

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

45 6 is contained within a predicted calmodulin-binding sequence and acetylation of Lys-306 strongly inh

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

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

48 ated the contributions of the 15-bp core Fis binding sequence and its flanking regions to Fis-DNA int

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

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

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

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

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

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

55 5 occupy enhancers that are enriched for ETS-binding sequences and are both functionally important fo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 Binding sequences are amplified by PCR using fluorescein

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

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

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

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

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

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

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 eover, Pak1 does not contain a canonical LC8 binding sequence compared with other characterized LC8 b

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

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

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

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

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

92 .5F proteins containing a scrambled integrin-binding sequence, demonstrating the importance of target

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 ntained the previously established consensus binding sequence for the respective proteins, thus attes

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

113 The binding sequence for the three substrates has been debat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 oid receptor (GR) interacts with specific GR-binding sequences (GBSs) at glucocorticoid response elem

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

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

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

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

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

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

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

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

140 ell-conserved RNA-binding domain and cognate binding sequence have been evolutionarily rewired to reg

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

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

143 imilarity to the T. pallidum TroR (TroR(Tp)) binding sequence; however, the position of this motif wi

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

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

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

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

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

149 We identified a short talin binding sequence in Lamellipodin (Lpd), another MRL prot

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

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

152 e molecule via binding to a noncanonical p53-binding sequence in the CD44 promoter.

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 Mutation of the putative RACK1 binding sequence in TRPC3 disrupted plasma membrane loca

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

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

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

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

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

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

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

172 possibilities, we used substrates with POT1-binding sequences in the single-stranded tail, duplex or

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 NA 3'-UTR sequence, and insertion of the p53-binding sequence into beta-globin mRNA destabilized the

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

179 east three mechanisms: (i) divergence of DNA-binding sequences into two subfamilies; (ii) condition-s

180 m this approach it would seem that a minimum binding sequence is a disulfated trisaccharide comprised

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

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

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

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

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

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

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

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

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

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

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

192 Transcript pattern clustering and a sigma(E)-binding sequence model were used to predict candidate pr

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

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

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

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

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

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

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

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

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

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

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

204 nus where RIM1beta lacks the N-terminal Rab3-binding sequence of RIM1alpha.

205 In comparison, the CaM-binding sequence of RyR1 remains conformationally disord

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

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

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

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

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

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

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

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

214 affinity in a collapsed structure to the CaM-binding sequences of both the Ca-ATPase and RyR1, result

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

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

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

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

219 Prior to CaM association, the CaM-binding sequences of the Ca-ATPase and RyR1 are conforma

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

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

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

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

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

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

226 98-602) clusters, forming accessible heparin binding sequences on the TG2 three-dimensional structure

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

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

229 nsensus regulatory element comprising a STAT-binding sequence overlapped by a binding-site for the tr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 ntage of the unique conserved Trp within CaM-binding sequences that functions as a hydrophobic anchor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

289 made in both half sites of a palindromic Fis binding sequence were examined for their effects on the

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 tional fusions constructed from specific Fur binding sequences within the fur promoter/operator regio

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

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

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