ライフサイエンスコーパス: consensus sequence

1 ind individual modules within a compound DNA consensus sequence.

2 length requirements and its phosphorylation consensus sequence.

3 r of ZF3-7 contacts three bases of the 15-bp consensus sequence.

4 scanning by Miz-1 during the search for its consensus sequence.

5 ome, and the sequence data generally yield a consensus sequence.

6 p53 binding site deviates from the canonical consensus sequence.

7 -generation sequencing in conjunction with a consensus sequence.

8 and an oligonucleotide complementary to the consensus sequence.

9 number of reads required to make a template consensus sequence.

10 tical to the modern North American subtype B consensus sequence.

11 omain of FOXM1 that inhibit binding to a FKH consensus sequence.

12 gulate target genes containing the CCAAT box consensus sequence.

13 l dsRNA duplex containing an OAS1 activation consensus sequence.

14 CRP(Mt) binding overlapped a palindromic consensus sequence.

15 a consequence, CDA-KLF1 did not bind the WT consensus sequence.

16 lerant recognition of other positions of the consensus sequence.

17 own TE families each represented by a single consensus sequence.

18 e O-glycosylation site is not within a known consensus sequence.

19 importance of the conserved bases within the consensus sequence.

20 sirtuins in yeast and found a shared target consensus sequence.

21 han half of which conform to a PKA substrate consensus sequence.

22 ma membrane, although it lacks a PDZ binding consensus sequence.

23 sequences can be thought of as generating a consensus sequence.

24 bility, as well as a set of highly permeable consensus sequences.

25 alternative splicing through binding to RNA consensus sequences.

26 moter mutations that create or disrupt GABPA consensus sequences.

27 and a bioinformatics pipeline for generating consensus sequences.

28 signals surrounding the exon to better match consensus sequences.

29 lecule and allows for efficient formation of consensus sequences.

30 in vivo often bind DNA regions lacking known consensus sequences.

31 s Pim and AKT protein kinase phosphorylation consensus sequences.

32 le sequencing strategies, including circular consensus sequencing.

33 which exhibits a strict requirement for the consensus sequence 5'-(A)/TTT(G)/C-3'.

34 an PRDM9, allele A (hPRDM9A), recognizes the consensus sequence 5'-NCCNCCNTNNCCNCN-3'.

35 tifs, and a target duplex DNA containing the consensus sequence 5'-TGGCGGGTTC-3'.

36 binds to over 500 operator regions with the consensus sequence 5'-TGGCSNGWWY-3' (where S is G or C,

37 promoter regions revealed a conserved, 6-bp consensus sequence (AAATGA).

38 that RFP was expressed from the appropriate consensus sequence AACGAA.

39 th this approach, we can achieve an improved consensus sequencing accuracy of 99.7% and resolve intra

40 ither upstream of or downstream from the ARS consensus sequence (ACS).

41 eractions compensate for deviations from the consensus sequence, allowing CTCF to adapt to sequence v

42 The consensus sequence also leads to pausing by RNAPs from d

43 C at sites characterized by a defined unique consensus sequence and particular features.

44 role of Miz-1 ZFs 1-4 in detecting the Miz-1 consensus sequence and preventing nonspecific DNA bindin

45 et of promoters that contain the methylation consensus sequence and show that loss of methylation wit

46 ural DNA sequences conforming to the class I consensus sequence and structure were found that undergo

47 grouped 2.9-12.8% of participants when using consensus sequences and 9.0-64.2% when using haplotypes.

48 9CA-CFTR, mutants that lack 15 PKA or 9 PKC consensus sequences and are unresponsive to PKA or PKC s

49 ommon secondary structure motif but distinct consensus sequences and positions within the respective

50 lated IMPs (ZBP1 and IMP2) bind to different consensus sequences and regulate targets consistent with

51 we generated de novo jockey retrotransposon consensus sequences and used phylogenetic tree-building

52 ferase reporter assays was dependent on Smad consensus sequences and was partially dependent on endog

53 uencing methodology based on PacBio circular consensus sequencing and the DADA2 sample inference meth

54 virus), between human hosts (3978 SARS-CoV-2 consensus sequences), and within human hosts (401 deeply

55 T387 lies in a cyclin-dependent kinase (CDK) consensus sequence, and CDK inhibitors decrease T387 pho

56 amino acid composition of the glycosylation consensus sequence, and cellular localization of target

57 Env7 contains a palmitoylation consensus sequence, and substitution of its three consec

58 aty-1 elements identical to their respective consensus sequence, and the presence of polymorphic elem

59 s, finding pairs of binding sites based on a consensus sequence, and, in some cases, identifying endo

60 ragment that contains two strong Gli-binding consensus sequences, and mutation of either site abrogat

61 ors recognize the same response element (RE) consensus sequences, and their transactivation of target

62 as a human-readable format for representing consensus sequences, and they remain widely used.

63 f AP-1 reporters occurred in a ligand-, AP-1 consensus sequence-, and AP-1 family member-specific man

64 Accurate RNA consensus sequencing (ARC-seq) uniquely combines RNA bar

65 GU-AG consensus sequences are used for intron recognition in t

66 i-partite nature of the ICP4 DNA recognition consensus sequence as the globular and disordered region

67 DNA binding domain complexed to the putative consensus sequence as well as an adjoining secondary seq

68 dress this, we developed a new single-strand consensus sequencing assay for the determination of HIV

69 Mutation of the single N-glycosylation consensus sequence at Asn-988 (Trpm4b-N988Q), located ne

70 f RNAs were identified that deviate from the consensus sequence at one or more of three positions dir

71 ignificantly better than those harboring the consensus sequence at this site, resulting in reduced re

72 lution that could be readily performed using consensus sequences available for other satellite famili

73 E. coli population in the samples, and build consensus sequences based on population allele frequency

74 at IRF8 is recruited to distinct sets of DNA consensus sequences before and after lipopolysaccharide

75 In this study, we found that the interferon consensus sequence binding protein (Icsbp/Irf8) was requ

76 ry factor 8 (IRF8), also known as interferon consensus sequence-binding protein, directly targets a l

77 Tyr126, which is part of the choline-binding consensus sequence but is found in direct contact with t

78 mediate transcriptional repression via Insv consensus sequences but that the ELBA complex appears to

79 tive elastin peptides presents the XGXPGXGXG consensus sequence, but the reason for their bioactivity

80 domains usually interact with a proline-rich consensus sequence, but the region of paramyosin that in

81 ic biology approach to demonstrate that this consensus sequence can direct acetylation and deacetylat

82 Viral consensus sequences can be achieved in 1-2 d by starting

83 ed that 9 of 12 TSRs with the O-fucosylation consensus sequence carried the Glucosebeta1-3Fucose disa

84 We report the optimization of circular consensus sequencing (CCS) to improve the accuracy of si

85 activate the eight variants of the 7-bp SMRE consensus sequence, composed of ACC(A/T)A(A/C)(T/C).

86 The method reproducibly generated the same consensus sequence, consistently identified viral sequen

87 hat specifically recognizes an 11-nucleotide consensus sequence consisting of two motifs in the promo

88 Motif analysis revealed a consensus sequence containing Sp1 binding motif signific

89 The assembled consensus sequences covered 99.3% to 100% of the HCV cod

90 rol via a cholesterol recognition amino acid consensus sequence (CRAC site).

91 nscriptome by binding the CREB1 binding site consensus sequence (CRE) sequence (TGACGTCA).

92 nts are predicted by realigning an assembled consensus sequence created from sequence reads that were

93 -fucosylation site did not meet the proposed consensus sequence CSX(S/T)CG.

94 Here, we identified a 12-bp consensus sequence [CT(G/T)CCAGGACCT] occupied by ZBTB24

95 obacter jejuni favors acceptor proteins with consensus sequences ((D/E)X1NX2(S/T), where X1,2 not equ

96 show that identified TTBK2 phosphosites and consensus sequence delineated from those are distinct fr

97 upstream of sco3205 and a pseudopalindromic consensus sequence derived from these enables further po

98 omologies revealed threonine at this site in consensus sequences derived from multiple-species alignm

99 Consensus sequence design offers a promising strategy fo

100 of accumulation of mutations in the genomic consensus sequence deviated slightly from linearity, and

101 c function RNA polymerase sigma factor RpoE2 consensus sequences displayed a sharp peak between -34 a

102 ausing occurs at sequences that resemble the consensus sequence element for transcription-elongation

103 nal exons and demonstrate a graded series of consensus sequence elements of varying strengths that se

104 Remarkably, two RNA 3 consensus sequences, encoding the nucleocapsid protein,

105 the AUG to improve their match to the Kozak consensus sequence enhanced Vhs cutting near the start c

106 ster than the existing pipelines, though the consensus sequence error rate is as high as raw reads.

107 two arginine residues directly recognize the consensus sequence, explaining the strict recognition of

108 NAviz implements a framework for determining consensus sequence features and can generate sequence fe

109 around the intron boundary and displays the consensus sequence features for all introns, small intro

110 ntical to those from honey bee tissues and a consensus sequence for A. mellifera.

111 A consensus sequence for Arc binding identifies several ad

112 of CAMTA1-mutant mice, and elucidation of a consensus sequence for binding of CAMTA proteins to DNA

113 A consensus sequence for each type of motif was determined

114 an intrinsic RNase activity and a potential consensus sequence for endonucleolytic cleavage identifi

115 phosphorylation at Ser204, fitting the known consensus sequence for GSK3 substrates.

116 o that of peptides, and the requirement of a consensus sequence for N-glycosylation further limits th

117 e-1 repeats (TSRs), six of which contain the consensus sequence for O-fucosylation by protein O-fucos

118 Although the current putative consensus sequence for O-GlcNAcylation predicts 18 O-Glc

119 ed genes in the sigH regulon with a putative consensus sequence for SigH binding that was recognized

120 transcribed from promoters containing a new consensus sequence for the human initiator (Inr) core pr

121 recognize several DNA substrates without the consensus sequence for YY1 in vitro, and DNA binding is

122 Our findings begin to define a consensus sequence for ZMPSTE24 that helps to clarify ho

123 we attempt to assess generality by designing consensus sequences for a set of six protein families wi

124 As seemed to be replicated and 80% contained consensus sequences for autonomous replication origins t

125 Several ADAMTSL2 TSRs also have consensus sequences for C-mannosylation.

126 The large number of consensus sequences for phosphorylation by PKA has natur

127 The consensus sequences for self-depurination of such G- and

128 ChIP-chip studies have provided conflicting consensus sequences for the FOXP2-binding site.

129 genome were sufficient to provide functional consensus sequences for the THAP domains, they do not sp

130 A subset of Six1-bound sites carry consensus-sequences for its downstream factors, includin

131 The consensus sequence from this alignment (Cfa) demonstrate

132 em repeat patterns and generate high-quality consensus sequences from amplified tandemly repeated lon

133 g; however, user-friendly software for build consensus sequences from molecule tagged reads is not re

134 analysis platform that generate accurate VP1 consensus sequences from multiplexed samples.

135 Here, we use 6717 HIV-1 consensus sequences from patients treated with first-lin

136 gnments including >110 000 HIV-1 partial pol consensus sequences from the UK HIV Drug Resistance Data

137 t associated with decreased infectivity, and consensus sequencing from tissues revealed no evidence o

138 ecognizes an alternative forkhead-like (FHL) consensus sequence (GACGC) that is different from the mo

139 cted by merging homologous loci into single "consensus" sequences, generally absent from nature.

140 Consensus sequences generated by different NGS methods w

141 Consensus sequences generated in the study can be used t

142 The structures revealed a 5-bp consensus sequence GGC(GC)|(CG) as the binding site for

143 ing a variety of ligands, two different AP-1 consensus sequences, GR and MR DNA-binding domain mutant

144 All GH31 enzymes share a consensus sequence harboring an aspartic acid residue as

145 based on a protein's primary sequence, but a consensus sequence has been slow to emerge.

146 erved within the first nuclear export signal consensus sequence identified in Saccharomyces cerevisia

147 eavage was dependent on the presence of a GG consensus sequence immediately before the cut site and a

148 mpensate to some extent for changes from the consensus sequence, implying an adaptability of PRDM9 to

149 cific promoter region featuring an NF-kappaB consensus sequence in a relevant subset of K17- and Aire

150 ly shifted from the previously reported CtrA consensus sequence in Caulobacter crescentus Bacterial o

151 we identified one or more copies of a 10-nt consensus sequence in each CAR.

152 ll 9 sites in patient B w ere present as the consensus sequence in patient A.

153 e-like CD8(+) T cells from patients with the consensus sequence in the corresponding T-cell epitope d

154 ssion was mediated by the HIF-1alpha-binding consensus sequence in the ErbB3 proximal promoter.

155 n the human genome, with deviations from the consensus sequence in the spacing, orientation, and exte

156 g to a putative antioxidant response element consensus sequence in the sterol regulatory-element bind

157 e report the role of a newly identified AP-1 consensus sequence in the TF gene promoter and its origi

158 mediated increased binding of Sp1 to the Sp1 consensus sequence in the Wnt9A promoter, shown by oligo

159 t six proteins, by specific recognition of a consensus sequence in them.

160 adds Glucosebeta1-3Fucose disaccharide to a consensus sequence in thrombospondin type 1 repeats (TSR

161 e the role(s) of individual cysteines of the consensus sequence in various properties of Env7 in vivo

162 We identified an EGPS consensus sequence in vIRF1, which is identical to that

163 The peptide length distribution and consensus sequences in axillary, brachial, inguinal, and

164 romoters encoding previously identified RpoD consensus sequences in B. burgdorferi.

165 We noted multiple E2F binding site consensus sequences in both promoters.

166 in the binding of STAT3 and STAT5 to shared consensus sequences in developing T cells.

167 Binding of NF-kappaB proteins to their consensus sequences in DNA (kappaB sites) is the key bio

168 tivators that compensate for the lack of -35 consensus sequences in N. meningitidis.

169 Binding to consensus sequences in the Atoh1 enhancer was dependent

170 ious lengths located between the -10 and -35 consensus sequences in the tp0126 promoter modulates tra

171 reviously described LXVP calcineurin-binding consensus sequence, increased the calcium-sensitivity of

172 Isolated peptides shared strong consensus sequences, indicating target-specific binding.

173 wintrons) are introns where any of the three consensus sequences involved in splicing is interrupted

174 uences such as 3'-TCC, TTC, and TTT, and the consensus sequence is 3'-Pu(Py)2-3 Based on our studies,

175 uggest that evolutionary conservation in the consensus sequence is driven by maintenance of the cleav

176 This consensus sequence is found in the toxic RNAs (CCUG repe

177 middle nucleotide, and the 3' portion of the consensus sequence is more degenerate.

178 However, we show here that the palindromic consensus sequence is not present in individual integrat

179 The known consensus sequence is observed to have the highest affin

180 d variants of the aptamers revealed that the consensus sequence is responsible and sufficient for bin

181 Binding to the deduced consensus sequence is supported by in vitro gel shifts a

182 nt with interactions involving GroEL binding consensus sequences located therein.

183 ence LVAEF with the evolutionarily conserved consensus sequence LVXEF.

184 e a six-residue "myristoylation signal" with consensus sequence: M(1)GXXX[ST].

185 deler2 identified approximately 3 times more consensus sequences matching with >95% sequence identity

186 Immunogens based on consensus sequences might have utility in engineering va

187 Although the consensus sequence motif has been identified and used to

188 ivergent PARP homology domain missing a PARP consensus sequence motif; the domain has enigmatic funct

189 Dozens of consensus sequence motifs containing predicted transcrip

190 1 brain promoter (ncx1-Br) has five putative consensus sequences, named Sp1A-E, for the specificity p

191 e of binding potency was only gained for the consensus sequence, not by the alanine insertion.

192 Mutational analysis verified consensus sequence nucleotides required for PmrA-directe

193 The class II substrates have the consensus sequence of (V/A)P(I/L/M/V/F)X1-6pY (where X i

194 nants we generated a SOSIP trimer based on a consensus sequence of all HIV-1 group M isolates (ConM).

195 ced is computationally processed to obtain a consensus sequence of all linked copies of the original

196 )), an amyloid-like peptide extracted from a consensus sequence of amyloidogenic proteins, which asse

197 the cleavage specificity of SBT4.13 and the consensus sequence of Arabidopsis SBTs at the junction o

198 the phosphothreonine residue of the pT-X-pY consensus sequence of ERK and p38 into Dhb and followed

199 Compared with a consensus sequence of June 18, 2014, the isolate that in

200 ine the genetic differences responsible, the consensus sequence of L10 was determined and compared to

201 The consensus sequence of many of the passaged samples had a

202 Thus, this work defines a consensus sequence of mechanochemical transitions that c

203 proteins containing docking motifs with the consensus sequence of PxIxIT.

204 The consensus sequence of RV-A16 from a previous inoculum wa

205 tein gene with a low-fusion RSV subgroup B F consensus sequence of the Buenos Aires clade (BAF).

206 ed samples had a 12 nucleotide insert in the consensus sequence of the spike gene, and multiple point

207 ies within each read are aligned to derive a consensus sequence of their initial RNA template.

208 or ToxR-dependent toxT activation revealed a consensus sequence of TNAAA-N(5)-TNAAA extending from -9

209 ovariance and fall into two classes with the consensus sequences of (D/E)EPIYvarphiXvarphi and (D/E)(

210 , while no heterogeneity was observed in the consensus sequences of additional genomic RNA segments.

211 The consensus sequences of H/PF/2013 and PRVABC59 differ by

212 s, but their sequences are inconsistent with consensus sequences of known HEAT modules, suggesting th

213 ucose occurred at high stoichiometry at most consensus sequences of NOTCH2 and that the Fringe enzyme

214 ides, HEAT_R1 and LRV_M3Delta1, based on the consensus sequences of single repeats of thermophilic HE

215 at which there were differences between the consensus sequences of the 2 linked viral genomes, 9 had

216 ull viral genome sequencing showed identical consensus sequences of the virus before and after cell c

217 Sporadic mutations were detected in the consensus sequences of the viruses after high-MOI passag

218 No mutations were detected in the consensus sequences of viruses collected from the bronch

219 EIV and CIV strains that were similar to the consensus sequences of viruses from each host.

220 Although a number of pooling strategies for consensus sequencing of DNA samples and detection of SNP

221 t augmented binding on cAMP response element consensus sequence on peroxisome proliferator-activated

222 o identify glycan modifications at predicted consensus sequences on mouse ADAMTSL2.

223 NA immunization with either a single HIV Env consensus sequence or multiple constructs expressing HIV

224 er alignments that displays motifs, as IUPAC consensus sequences or position frequency matrices, in t

225 utating BDF2 5' splice site and branch point consensus sequences partially suppresses the bdf1Delta t

226 and/or enterobacterial repetitive intergenic consensus sequence PCR (ERIC-PCR) was performed.

227 e-Rich (SRCR) domains, localized to a 16-mer consensus sequence peptide, SRCRP2.

228 However, individual or pooled consensus sequence peptides (SRCRPs 1 to 7) showed no ac

229 ubstantial tolerance for deviations from the consensus sequence, plus requirements at some positions

230 Improving consensus sequences ('polishing') with Nanopolish somewh

231 ctor U2AF(65) normally recognizes a Py tract consensus sequence preceding the major class of 3' splic

232 ized, on the basis of an Akt phosphorylation consensus sequence present in HK-II, that Thr-473 is the

233 a strain-DBN coding sequence, modified NS5B consensus sequence, pS52 untranslated regions, and codin

234 our data show that the previously described consensus sequence PXRPXR for amphiphysin SH3 ligands is

235 ncy, we find a highly enriched messenger RNA consensus sequence, R-motif, consisting of mostly purine

236 Using DuploMap-aligned PacBio circular consensus sequencing reads, an additional 8.9 Mb of DNA

237 Disruption of the NES consensus sequence relocalizes mutant SOD1 to the nucleu

238 beta from wheat, OsRca-beta from rice, and a consensus sequence representing Rca from warm-adapted sp

239 entification of the class of RNA cleaved and consensus sequences required for accurate substrate reco

240 Part of the CATAC consensus sequence resembles the E-box binding site for

241 reads derived from at least 7 full circular consensus sequencing rounds significantly reduced the in

242 This motif is characterized by the consensus sequence Rx[Gnl]x(1-2)Wxxx[Arlv]x[Dn][Rg]xRFxx

243 nown about influenza evolution has come from consensus sequences sampled at the epidemiological scale

244 am produces a 2.9% increase in coverage over consensus sequence search methods on a large human bench

245 genes for whole Gag, Env, and Nef as clade B consensus sequences (separate injection sites).

246 opy studies and binding studies with mutated consensus sequences showed that the sequence was importa

247 nd to bind chromosome tightly, likely at non-consensus sequence sites.

248 epeated five-residue (Rfr) folds with an Rfr consensus sequence (STAV)(D/N)(L/F)(S/T/R)(X).

249 protein complex that binds the NF-kappaB DNA consensus sequence, strengthening the idea of an associa

250 oration of the contemporary strain epitope D consensus sequence STT improved ligand binding relative

251 A that extends beyond the proposed canonical consensus sequence suggesting a more complex level of re

252 ock wild-type MYOD1 function and bind to MYC consensus sequences, suggesting a possible switch from d

253 ate strand bases of a conserved -10 element (consensus sequence T-12A-11T-10A-9A-8T-7) is an importan

254 5-46(G54W) arising from mutations in a gp120 consensus sequence, targets a common route of HIV-1 esca

255 aining the biologically-relevant Pribnow box consensus sequence 'TATAAT'.

256 en access a site 40 residues distal from the consensus sequence that collectively direct phosphorylat

257 Point centromeres are specified by a short consensus sequence that seeds kinetochore formation, whe

258 species of Drosophila, we discovered a 29-bp consensus sequence that we designated as the Clock-Assoc

259 Promoters are short DNA consensus sequences that are localized proximal to the t

260 biosensors for diverse ligands and determine consensus sequences that enable ligand-responsive tertia

261 The repeat was reconstructed into three consensus sequences that formed three interconnected loo

262 Human genomes are typically assembled as consensus sequences that lack information on parental ha

263 By using 7 passes of circular consensus sequencing, the error rate was reduced to 0.37

264 ach of the six early proteins and generating consensus sequences to represent five hrHPV genotypes.

265 only two tRNA isoacceptors containing the GG consensus sequence, tRNA(Gln32-CUG) and tRNA(Leu3-CAG).

266 , and its promoter contains all the putative consensus sequences typical of eukaryotic promoters, bei

267 onserved heptapeptide repeats containing the consensus sequence Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7.

268 describe valuable data that are missing from consensus sequences, variable effects on sequence data g

269 r domain, and we characterize its tripartite consensus sequence via SELEX (systematic evolution of li

270 ificity for Pro-Pro peptide bonds within the consensus sequence VNP PVP.

271 th high specificity and affinity to the WRKY consensus sequence (W-box), and also to its own promoter

272 The accuracy of the generated consensus sequence was estimated to be >99% based on res

273 nstructs expressing HIV subtype-specific Env consensus sequences, we detected both CD4(+) and CD8(+)

274 , Miz1-4(WT) was found to bind the Miz-1 DNA consensus sequence weakly and through ZFs 1-3 only.

275 ACE-PCR), and strong sigma(54) and sigma(70) consensus sequences were identified at PampR and PampC,

276 We found that HA consensus sequences were similar in nonvaccinated and va

277 Pol region consensus sequences were used for phylogenetic analysis.

278 (strains DH8 and DH10), and 2c (strain S83) consensus sequences, were viable in Huh7.5 hepatoma cell

279 Sequence analysis revealed a single consensus sequence, which could be phylogenetically assi

280 to the secondary wall MYB-responsive element consensus sequence, which encompasses the AC elements, t

281 s resulted in the identification of a G-rich consensus sequence, which was able to fold in a typical

282 ified and validated a putative RpoE promoter consensus sequence, which was enriched in the majority o

283 ine phosphorylation within the RNP1 and RNP2 consensus sequences, which coordinate RNA binding - sugg

284 olishing tool, Racon, generates high-quality consensus sequences while providing a significant speedu

285 ese tandem sequences can be collapsed into a consensus sequence with a higher accuracy than the origi

286 in of latent transcript of CyHV-3 contains a consensus sequence with homology to a conserved domain o

287 The hypothetical protein of ORF6 contains a consensus sequence with homology to a conserved domain o

288 , E6 binds to a short leucine (L)-rich LxxLL consensus sequence within the cellular ubiquitin ligase

289 A consensus sequence within Wnt3a was identified (CXCHGXSX

290 ral native glycoproteins are known to harbor consensus sequences within structured regions of the acc

291 that 6 of the genes contained HP1043 binding consensus sequences within the promoter regions (fur, ca

292 ard unique molecular identifier (UMI)-linked consensus sequencing workflow (UMIC-seq) that simplifies

293 nding position is dictated by an established consensus sequence (WWN9WG).

294 identified a novel conserved region with the consensus sequence WWxxRxxLD predicted to be exposed on

295 is composed of tandem heptad repeats of the consensus sequence Y(1)S(2)P(3)T(4)S(5)P(6)S(7).

296 the heptad repeats of which it is composed (consensus sequence Y1S2P3T4S5P6S7).

297 inal domain (CTD) composed of heptads of the consensus sequence YSPTSPS.

298 mposed of tandemly repeated heptads with the consensus sequence YSPTSPS.

299 Hexapeptides of consensus sequence YXCXXC displace four fluorine atoms f

300 4E-Transporter binds eIF4E via its consensus sequence YXXXXLPhi, shared with eIF4G, and is