ライフサイエンスコーパス: motif

1 ation depending on its C-terminal activation motif.

2 ingle regulatory factor or promoter sequence motif.

3 the phosphatase via a conserved short linear motif.

4 genes predicted to be regulated via an ER-2 motif.

5 a 24-kDa brain-enriched protein with a SNARE motif.

6 and directly dephosphorylates the T788/T789 motif.

7 r gene due to the absence of a Keap1-binding motif.

8 transcriptional coactivator with PDZ-binding motif.

9 effects of nucleotides beyond the core CTCF motif.

10 ndensation to deliver the (dihydro-)pyridone motif.

11 et sequence in tandem with the APT silencing motif.

12 containing a highly conserved twin-arginine motif.

13 diates stable binding to a non-canonical DNA motif.

14 ch we previously identified as a CDK-binding motif.

15 ntain the pyrrolodiketopiperazine structural motif.

16 site defined by a conserved Asp-His-His-Cys motif.

17 richment of the transcription factor binding motif.

18 ated by affinity and position of B56 binding motifs.

19 ould be an ideal approach to construct these motifs.

20 ing (SMC), resulting in new-to-nature biaryl motifs.

21 Pyridine rings are prominent amongst these motifs.

22 reshold followed by a list of glycan-binding motifs.

23 ory sequences and transcription factors (TF) motifs.

24 l regions at Serine/Threonine-Glutamine (SQ) motifs.

25 including proapoptotic genes, have weak ISRE motifs.

26 lux via phosphorylation at conserved, shared motifs.

27 anonical surface-exposed Tyr-based endocytic motifs.

28 oding regions near known amoxicillin binding motifs.

29 tangle reciprocal and feedforward-inhibitory motifs.

30 ding of suramin to the "AT-hook" DNA-binding motifs.

31 tion of high- and low-temperature structural motifs.

32 ions with non-canonical protospacer-adjacent motifs.

33 nd the synthesis of complex antennary glycan motifs.

34 tors that predominantly bind exonic splicing motifs.

35 aining logic gates linked to self-immolative motifs.

36 Ps can bind to multiple distinctly different motifs.

37 sed immunogens displaying complex structural motifs.

38 folds and conformity to conserved structural motifs.

39 y between financial incentives and intrinsic motives.

40 led significant changes only for RNA-binding motif 3 (Rbm3).

41 CA2;3, a binding partner of CDKB1;1, via SIM motif A, which we previously identified as a CDK-binding

42 r overall architecture and phosphate binding motif, a lack of sequence identity and some fundamental

43 utations of Ets or E-box sites in either DNA motif abolished the activation and reduced or eliminated

44 and identified a novel RFC1 repeat expansion motif, (ACAGG)exp, in three affected individuals.

45 Motif activity analysis showed that both promoters and e

46 The critical Set1 RxxxRR motif adopts a helix that mediates bridging contacts bet

47 eract with Atg8a using four Atg8-interacting motifs (AIMs) located at the C-terminus, cytoplasmic loo

48 oteins via the recognition of functional Tyr motifs also operates in plants.

49 generated mice with an inactivated mIgE-ITT motif and analyzed serum IgE levels as well as the gener

50 the AtSRBP1-4 (AtGRP7/2/4/8) RNA recognition motif and GR domains.

51 Sterile alpha motif and histidine-aspartic acid domain-containing prot

52 inhibition between ChINs is a robust network motif and instrumental in shaping the network activity o

53 nique hydrogen peroxide (H(2) O(2) )-sensing motif and its capacity for providing cellular protection

54 E3 ligase complex, such as the zinc-binding motif and N- and C-terminal regions of the protein.

55 ement for simultaneous recognition of the pY motif and the surrounding folded protein epitope.

56 ely remained conserved in canonical sequence motifs and copy numbers as in E. maclovinus, showing lim

57 nces containing their respective DNA-binding motifs and identify preferential motif arrangements that

58 cture that recognizes linear phosphotyrosine motifs and is present in a wide range of signaling pathw

59 nt concepts to eliminate unwanted structural motifs and to improve the inhibitor characteristics of t

60 ealed that the RILP algorithm selected fewer motifs and was able to cover 6% more peaks and 3% fewer

61 regions were strongly enriched for the AP-1 motif, and indeed, ChIP-seq demonstrated AP-1 binding at

62 ed MamY and the actin-like MamK via distinct motifs, and with the cell shape-related cytoskeleton via

63 the pleckstrin homology domain and the SNARE motif are needed for its inhibitory function.

64 Terminal Galalpha1-3Gal motifs are found as a defining feature of different bloo

65 These motifs are highly specific with implications for both si

66 These dimeric structural motifs are important building blocks for the total synth

67 ds, a number of novel lipophilicity-reducing motifs are introduced.

68 The binding of Fpr to various DNA motifs are mediated by its flat DNA-binding surface, whi

69 mplete: typically, around 40% of susceptible motifs are modified.

70 However, it is unclear which motifs are prone to impact transcriptional regulation if

71 Feedback inhibitory motifs are thought to be important for pattern separatio

72 ype of C(60/70) host where electron-rich PDI motifs are utilized as recognition motifs for fullerenes

73 DNA-binding motifs and identify preferential motif arrangements that influence accessibility.

74 The proteins associate with the RNA C-rich motif as a 1:1:1 complex.

75 , 9, and 13 to validate the vicinal difluoro motif as a hybrid bioisostere of CF(3) and Et (BITE) in

76 ally challenging spirocyclic tetrahydrofuran motif as well as several other key stereochemical proble

77 s9-independent off-targeting and point to TC motifs as activity hotspots of the cytidine deaminase us

78 le to identify a number of promoter sequence motifs associated with leaf senescence.

79 ere by demonstrating that the analogous ATF4 motif at the murine Bcl11a enhancer is largely dispensab

80 ples a graph mining-based strategy to detect motifs at the protein-ligand interface with an interacti

81 e targeting probability of a nucleotide in a motif-based fashion, assuming that the same DNA motif is

82 MBC-like WM hypomethylation was enriched in motifs belonging to PU.1, TCF3, and OCT2 transcription f

83 esults demonstrate that although some common motifs between the HIV-1 Vif and MVV Vif are involved in

84 We find that these 'secondary motifs' bind Rbfox robustly in cells and that several to

85 ximately 70% of RBPs for which we obtained a motif bound to short linear sequences, whereas ~30% pref

86 The methylation motif CACNNNNNTAC was only found in isolates of sublinea

87 or a classification of minimal autocatalytic motifs called cores.

88 Our results demonstrate that simple sequence motifs can rigidify elementary membrane proteins, and th

89 conferred by low affinity pMad/Medea binding motifs, can contribute to the specification of BMP targe

90 Each motif captured a unique spatiotemporal pattern of neural

91 ecies, and the presence of the canonical CDK motif, CDKB emerged as a likely candidate for a Saccharo

92 asin P672 that physically interacts with C-C motif chemokine ligand (CCL) 8 and synthesized a 16-mer

93 rosis factor alpha, interleukin-6, and C-X-C motif chemokine ligand 1 expression.

94 +) T cells through the downregulation of C-C motif chemokine receptor 5 (CCR5) in T cells and CD4 in

95 er characterized by the transcription factor motif codes of their promoters.

96 forward inhibition was weakened, and the two motifs combined to modulate fusiform cell output and aco

97 ferential genomic regions, identifying E-box motifs common to epithelial-mesenchymal transition drive

98 ical studies of single WW domain-single PPXY motif complexes abound in the literature, the molecular

99 in vitro confirmed that residues in sequence motifs conserved across bacterial and eukaryotic ortholo

100 he development of miCas9 by fusing a minimal motif consisting of thirty-six amino acids to spCas9.

101 sequences are predicted to have possible NES motifs containing cancer-related mutations at their key

102 ial homolog of transmembrane BAX inhibitor-1 motif-containing 6 (TMBIM6) membrane protein that plays

103 Here, we show that an AT-hook motif-containing nuclear localized (AHL) protein regulat

104 terile alpha and Toll/interleukin-1 receptor motif-containing protein 1 (SARM1) is a central regulato

105 scope with all six-carbon-substituted arene motifs, control experiments, and gram-scale synthesis ma

106 an additional GXXXG helix-helix interaction motif created in the mutant hairpin.

107 The 2H phosphoesterase motif defines an evolutionarily ancient protein domain p

108 A sequence motif defining these families, the X position in the CXC

109 date and is the first PI with CS-alpha/beta motif described from animal venoms.

110 : designs sequences that fold onto novel RNA motifs (described by tree graph topologies).

111 ine that variants of the TOP domain finger 1 motif destabilizes the channel structure and impairs cha

112 While the orientation of CTCF motifs determines which pairs of CTCF sites preferential

113 onding situation of the central C(2) in this motif differs remarkably from that of free C(2).

114 ion, followed by sequencing analysis and DNA motif discovery.

115 ibitor Sic1, contains linear phosphorylation motifs, docking sites, and phosphodegrons to empower an

116 ion, while cluster binding to the N-terminal motif does not affect the quaternary structure of NUBP1.

117 e find that the arginine residue in the FLVR motif does not directly contact pTyr(1087) of a bound ph

118 pentaloop is recognized by the sterile alpha motif domain-containing ZCCHC14 protein, which in turn r

119 Another motif, DPHK, is in the DNA-binding domain.

120 stereochemistry of the vicinal amino alcohol motif embedded within the targets.

121 ntibodies (Abs) against phosphotyrosine (pY) motifs embedded in folded polypeptides remains highly ch

122 u-721, and Leu-725, that are part of a novel motif, EXEXXXL(725), critical for PC7 activity on hTfR1.

123 these data demonstrate that discrete glycan motifs expressed on CD11b/CD18 such as biantennary galac

124 sequences, whereas ~30% preferred structured motifs folding into stem-loops.

125 ke (S) glycoprotein exhibits a high-affinity motif for binding TCRs, and may form a ternary complex w

126 lular N terminus, which contains the binding motif for endogenous Src tyrosine kinase that constituti

127 nd that EBV gH/gL does not utilize a similar motif for fusion activity.

128 bly uncovered a transcription factor-binding motif for ZNF263, a C2H2 zinc finger protein.

129 -rich PDI motifs are utilized as recognition motifs for fullerenes, facilitating novel intermolecular

130 extracellular loops as important structural motifs for ion selectivity and channel inhibition in Pan

131 Aberrant CTCF binding was enriched for motifs for key myeloid transcription factors such as CEB

132 es so by rediscovering ab initio the binding motifs for known regulators and some unknown ones.

133 many CAPs associate, although each contains motifs for only a minority of the numerous associated tr

134 gets depended on the presence of DNA binding motifs for other TFs, including TCF1.

135 ulators, which often feature carboxylic acid motifs for target engagement, have emerged as a class of

136 expand the current catalogue of DNA sequence motifs for transcription factors, and describe motifs th

137 ted whether retributive and consequentialist motives for punishment are present in children approxima

138 f modification and its position within the i-motif forming sequence.

139 Furthermore, i-motif forming sequences stable at neutral pH were signif

140 netically modified than traditional acidic i-motif forming sequences.

141 ture exhibits similarity to eIF3 recognizing motifs found in hepatitis C virus (HCV)-like IRESs, sugg

142 residues from CTD and the His-Cys-His (HCH) motif from the N-terminal segment of the neighboring sub

143 esigned by using only examples of structural motifs from unrelated proteins.

144 These motifs generalized across animals and were seen in multi

145 G6) and lysine (K7) residues of the Walker A motif (-GPAGTG(6)K(7)S-) were found to be critical to th

146 since the relevant PLK1 and PP2A-B56 binding motifs have coevolved in the same region on MADBUB homol

147 d Galpha(q) These findings indicate that GBA motifs have versatility in their G-protein-modulating ef

148 yotic cell division, cyclin-specific docking motifs help cyclin-dependent kinases (CDKs) phosphorylat

149 is a powerful tool for accessing structural motifs, highly desirable by the pharmaceutical industry.

150 etion of Cav-1 scaffold domain binding (CSD) motif in EphB1 prevented EphB1 binding to Cav-1 as well

151 side chain of Glu89 (located along the arch motif in hExo1) flips frequently from the reactant state

152 ha-Linked galactose is a common carbohydrate motif in nature that is processed by a variety of glycos

153 yristoylation signal and the C-terminal FXXF motif in PKAc regulate its thermal stability and catalys

154 c phenotypes identifies a novel KLTF peptide motif in the Cik1 N-terminus.

155 ing RNA (ncRNA) genes via a SUMO-interacting motif in the HDAC Cpr1 subunit.

156 the pore concomitant with bending of a GGxGG motif in the pore helices.

157 YAP association with the TEA domain-binding motif in the promoter region of inflammatory cytokines.

158 es and establishing links between structural motifs in a catalyst, local electronic structure, and ca

159 Fluorinated alkyl groups are important motifs in bioactive compounds, positively influencing ph

160 X for short, to bind certain DNA recognition motifs in gene promoters that regulate gene expression.

161 form to visually explore and interpret these motifs in the context of protein-ligand interfaces.

162 e demonstrate that the integrity of the CCHC motifs in the Gag NC domain is dispensable for Alix-medi

163 analyze paired transcription factor binding motifs in the promoters of cell type-specific genes.

164 er-to-order transition of the ankyrin repeat motifs in the substrate binding domain of cpSRP43 drives

165 named for conserved Pro-Glu and Pro-Pro-Glu motifs in their N termini.

166 on (LIR) docking site (LDS) in ATG8s and LIR motifs in various interaction partners.

167 To test for MeCP2 binding to these motifs in vivo, we analysed human neuronal cells using C

168 These k-mers represented the characteristic motifs (in the form of a collection of conserved short p

169 containing Ga-arene and Ga-OTf coordination motifs, in addition to an unusual "naked" [Ga](+) ion, a

170 image, but also by instrumental or strategic motives, in anticipation of future misbehavior.

171 rks, consisting of multiple forms of circuit motifs including reciprocal (inhibitory interneurons inh

172 Here, we find new connectivity motifs, including axo-axonic connectivity between projec

173 e B analogues equipped with novel structural motifs, including fluorine-containing residues, 12,13-di

174 ruption of TF (transcription factor)-binding motifs, inferred from alternative alleles at the haQTLs,

175 Here, we investigate how a benzene motif influences the photoinduced electrocyclization of

176 ted, only the bromodomain and extra-terminal motif inhibitor CPI203 enhanced the expansion of human c

177 evealed an EF domain with two Ca(2+)-binding motifs inserted within the catalytic domain.

178 otein interactions using the conservation of motifs, interology, or presence or absence of key sequen

179 gether, our data argue that the high mannose motif is an infection-associated molecular pattern on ho

180 itor based on a P1-P3 macrocyclic tripeptide motif is described.

181 if-based fashion, assuming that the same DNA motif is equally likely to be targeted regardless of its

182 We found that the KSHV gH (ELEFN(50-54)) motif is important for higher KSHV fusion and that EBV g

183 [4Fe-4S](2+) cluster bound at the C-terminal motif is labile.

184 A similar motif is present in a number of established and newly id

185 This motif is present in another (p)ppGpp target, the purine

186 The d(CGA) triplet repeat motif is structurally dynamic and can transition between

187 Our findings indicate that the twin-His motif is the core structure responsible for substrate de

188 relative prevalence of different reciprocity motives is highly stable across participant samples.

189 ng these families, the X position in the CXC motif, is not predicted to make significant contacts wit

190 ing immunoreceptor tyrosine-based activation motifs (ITAM) in both these receptors.

191 n synthesis, is the most abundant regulatory motif known to biology.

192 of the CNN confirmed it detects familiar DNA motifs known to correlate with real variation, like homo

193 collisions were enriched on diverse sequence motifs known to slow translation.

194 isomerization of, Kv4.2 at the pThr(607)-Pro motif, leading to the dissociation of the Kv4.2-DPP6 com

195 4, and PAR1:CXCR4 heteromers, chemokine (CXC motif) ligand 12 stimulation reduced surface expression

196 ecede or are independent from chemokine (C-C motif) ligand-CCR2 signaling in the development of age-r

197 associated with high levels of chemokine C-C motif ligands 17 and 22.

198 ructure incorporating a protonated hydrazone motif linked to the 1,2,5-oxadiazole 2-oxide subunit was

199 Plants evolved lysine motif (LysM) receptors to recognize and parse microbial

200 Mechanistically, the proline-rich motif-mediated interaction of PRR11 with the p85alpha re

201 atory signaling in response to the bacterial motif muramyl dipeptide.

202 s through increasing the accessibility of TF motifs NR1H4 and OLIG (OLIGI and OLIG2), respectively.

203 In Arabidopsis thaliana, the AT-hook motif nuclear-localized (AHL) transcription factor famil

204 However, unlike synaptrobrevin-2, the SNARE motif of amisyn is not sufficient to account for the rol

205 e amino acid substitution in the coiled-coil motif of BRCA1.

206 inpointed Met-1669 as the residue in the GBA motif of DAPLE that diverges from that in GIV and enable

207 the interface of 14-3-3 with the recognition motif of either the tumor suppressor protein p53 or the

208 x, (ii) PRV DNA G-quadruplex, and (iii) an i-motif of human telomeric sequence.

209 inhibits I(Kv1.5) Disrupting the Src-binding motif of Kv1.5 through N-terminal truncation or mutagene

210 4Fe-4S](2+) cluster formed at the N-terminal motif of NUBP1 is tightly bound, while the [4Fe-4S](2+)

211 s process, cluster binding to the C-terminal motif of NUBP1 promotes protein dimerization, while clus

212 o acid residues are a potentially targetable motif of TIMP-1 oncogenic activity.

213 ingle nucleotide mutation of m(6)A consensus motif of viral RNAs enhances RIG-I sensing activity.

214 Gibbs clustering was performed to identify motifs of binding peptides.

215 Importantly, four motifs of conserved nucleotide sequences (CNSs) were als

216 Our results suggest that the basic motifs of cortical dynamics emerge as a consequence of t

217 his allowed us to characterize DNA consensus motifs of early and late ASFV core promoters, as well as

218 Our analysis extends the known motifs of protein-adenine interactions in the Watson-Cri

219 issue-specific NFR were enriched for binding motifs of transcription factors related to tissue-specif

220 d ability to sequence homopolymers, repeated motifs or long-range structural variation, and long-read

221 lexibility of the linker between two binding motifs, our results suggest that the conformational fluc

222 l screens to assess the protospacer adjacent motif (PAM) and guide RNA (gRNA) requirements of 79 Cas9

223 ers and the cleavage of protospacer adjacent motif (PAM) in several type I CRISPR-Cas systems, but ho

224 Due to protospacer adjacent motif (PAM) requirements, CRISPR/Cas9 cannot access many

225 to contain any specific protospacer-adjacent motifs (PAM); is a multi-turnover enzyme; cleaves ssDNA,

226 Mutating subsets of both motifs partially alleviates non-productive splicing.

227 , TEs abundant in these regions and carrying motifs potentially beneficial for enhancer architecture

228 rate that FDL1 directly binds to CCAACC core motifs present in AD1 regulatory regions to activate its

229 that k-gram statistics with visibility graph motifs produce fast and accurate classifications, highli

230 Although conventionally defined as AG-rich motifs, recent genomic surveys reveal great sequence div

231 and it is not known whether the plant lysin-motif receptor-like kinase MtLYK10 intervenes in recogni

232 s of natural and engineered chemokine (C-X-C motif) receptor 4 (CXCR4) agonists in a rat acute respir

233 ouble-sized defensin, predicted to possess 2 motifs related to beta-defensins and 6 disulfide bridges

234 meter of 2 nm, as long as the glycine zipper motif remains intact.

235 Here, we comprehensively analyze LP motif requirements in vivo by combining a competitive gr

236 s in cells reveal that LD targeting of these motifs requires deeply inserted tryptophans that have lo

237 We solved separate NMR structures of the IQ motif (residues 1,646-1,664) bound to alpha-actinin-1 an

238 star possessing three and six cavitand-based motifs, respectively, demonstrates that such self-assemb

239 g dsDNA and DNA strand separation by the ThM motif, revealing an unconventional DNA unwinding mechani

240 ions with target genes, and were enriched in motif-rewiring mutations and structural variants.

241 e arginyl-glycyl-aspartic acid cell adhesion motif RGD, which can be used as coating, but can also be

242 we report a mutation in the RNA recognition motif (RRM) of CSTF2 that changes an aspartic acid at po

243 TIA1 contains three RNA recognition motifs (RRMs) and a C-terminal low-complexity domain, so

244 nd a bipartite motif, termed SNX-BAR-binding motif (SBM), in the cargoes.

245 amming suggests a correlation of recognition motif sequence and spacing that may distinguish producti

246 Multiple copies of WW domains and PPXY motif sequences are often reciprocally presented by regu

247 to a central core region that depends on the motif sequences of our previously nominated driver DAPs.

248 18 ULK1-specific and 7 ULK2-specific protein motifs serving as different interaction interfaces.

249 red immunoreceptor tyrosine-based activation motif signaling.

250 terminal region containing SUMO Interactions Motifs (SIMs) required to bind SUMO modified substrates.

251 Short linear motifs (SLiMs) drive dynamic protein-protein interaction

252 In this paper, we focus on the role of motifs (specifically, FFLs) in signal propagation in TRN

253 phase separation reduces the requirement for motif specificity and expands the repertoire of substrat

254 e sensitive information about the underlying motif structure.

255 dentifies a GC-rich region as SERBP1-binding motif; subsequent genomic and functional analyses establ

256 ns also carry multiple "AT-hook" DNA-binding motifs, suramin is expected to inhibit HMGA1-DNA interac

257 Phosphorylation of a conserved threonine motif (T788/T789) in the integrin beta cytoplasmic domai

258 transcriptional coactivator with PDZ-binding motif (Taz), two transcriptional coactivators known to b

259 (PX) domain of SNX5 or SNX6 and a bipartite motif, termed SNX-BAR-binding motif (SBM), in the cargoe

260 4A1 has a functional destruction box (D-box) motif that allows binding with two APC adaptors, CDC20-h

261 ses a mimic of an eukaryotic ATG16L1-binding motif that binds to ATG16L1's WD40 domain.

262 A structural motif that is found in two cancer drugs may be responsib

263 membrane proteins contain conserved sequence motifs that are known to be important in helix packing.

264 heir function and elucidating key structural motifs that can be targeted for therapeutic regulation.

265 ence-and predict further properties of these motifs that can be tested in future experiments.

266 tifs for transcription factors, and describe motifs that correspond to other transcription factors th

267 nterneurons, with stereotypical connectivity motifs that may follow specific plasticity rules.

268 While binding to the same consensus motif, their DNA-binding syntax is different, suggesting

269 ng a conformation that can bind specific DNA motifs, thereby serving to either activate or repress tr

270 NA-protein interactions from outside binding motifs through altered RNA secondary structure.

271 us NPs contain a highly conserved DEDDh ExoN motif, through which LASV NP degrades virus-derived, imm

272 ze with a speckle-associated RNA recognition motif to promote speckle specificity and residence.

273 zymes to synthetic catalysts, exert adaptive motifs to maximize their functionality.

274 us subcellular regions via sequence specific motifs to measure spatiotemporal changes in ERK activity

275 mmalian reovirus, mimic extracellular matrix motifs to specifically interact with the host membrane.

276 ITAM, ITIM or ITSM tyrosine phosphorylation motifs to the promiscuous cell-surface phosphatase CD45(

277 agement between RNA helicases and tripartite motif (TRIM) E3 ligases that lead to their functional co

278 polyglutamine-adjacent ubiquitin-interacting motifs (UIMs) that enhance aggregation and toxicity.

279 ded preinitiation complex that binds to TATT motifs unique to EBV late lytic promoters.

280 ein pair, the isoform bearing the leucoplast motif usually has greater root protein abundance.

281 These simulations indicate that Motif V controls communication between the ATP-binding p

282 e specifically, mutations T407A and S411A in motif V exhibit a hyperactive helicase phenotype, leadin

283 We tested Motif V mutations in both the replicon and recombinant p

284 The most frequently broken motif was REST (p value = 0.0028), which has been report

285 tecture, carrying five molecular beacon-like motifs, was constructed to display ten dengue envelope p

286 Using this motif, we identified over 70 putative SNX-BAR ligands, m

287 The confidently identified NES candidate motifs were checked for overlap with cancer-related muta

288 -stimulated response element (ISRE) promoter motifs, whereas the expanded set of type I IFN-specific

289 g the informational content of functional HS motifs which is crucial for their future biomedical expl

290 factor (TF) binding by mutating a TF binding motif, which in turn may affect the activity of the regu

291 The deletions of two critical motifs, which interact with the members of cellular FXR

292 it is clear that changing a protein binding motif will alter protein binding, it has been shown that

293 rystal structure of the W C-terminal binding motif with 14-3-3 provides only the second structure of

294 This inhibition depends on a unique motif with conserved serine and threonine (S/T) residues

295 ion hubs, it contains repeated neurochemical motifs with distinct inputs: GABA-rich modules are inner

296 on for the resolution of outer arm structure motifs with recognized biological functions.

297 dotoxin, indicating that targeting of DVRGLL motif within MYLK-L may limit SOCE-induced vascular hype

298 the DBD and the multiple phosphorylated AD2 motifs within the tetramer.

299 replication by directly binding to specific motifs within their promoters.

300 YtgR levels through a rare triple-tryptophan motif (WWW) in the YtgCR precursor.