ライフサイエンスコーパス: binding motif

1 g that LvgA recognizes more than one type of binding motif.

2 sphorylatable residues within a reported SH3-binding motif.

3 ed design starting from a known kinase hinge binding motif.

4 ing to position E23 serve as the core of the binding motif.

5 angement of the nucleosomal array around the binding motif.

6 mplification via an intracellular calmodulin-binding motif.

7 rrelated with the NR4A3 transcription factor binding motif.

8 tructural adjustment of the periplasmic TonB-binding motif.

9 of KRAS4b, which might represent a novel CaM-binding motif.

10 arvesting complexes, including a chlorophyll-binding motif.

11 ecognition cap and hydroxamic acid as a zinc-binding motif.

12 eraction was mediated by an N-terminal UAP56-binding motif.

13 in in Sgo1 in close proximity to the cohesin-binding motif.

14 ctivation of a reporter with a FOXP2-derived binding motif.

15 encode proteins with a helix-turn-helix DNA-binding motif.

16 evealing a new role for this protein-protein binding motif.

17 e MSL complex by de novo acquisition of this binding motif.

18 died using short peptides recapitulating the binding motif.

19 reporter gene due to the absence of a Keap1-binding motif.

20 a a nonclassical, potentially catalytic zinc-binding motif.

21 ient for binding and defines the minimal CaM-binding motif.

22 protein/transcriptional coactivator with PDZ-binding motif.

23 nserved K-segment, proposed to be a membrane-binding motif.

24 ordered state and lacks any recognizable RNA-binding motif.

25 f A, which we previously identified as a CDK-binding motif.

26 nsight into this less-well-understood 14-3-3 binding motif.

27 ors due to biases in CpG enrichment in their binding motif.

28 e Walker A sequence, a well-known nucleotide-binding motif.

29 n CpG enrichment of the transcription factor binding motif.

30 s 2 to 8 of the N-proximal arginine-rich RNA binding motif.

31 2, which contains a conserved Y(X)4LPhi IF4E-binding-motif.

32 er modulated by affinity and position of B56 binding motifs.

33 based on their size, polarity, and specific binding motifs.

34 as is enrichment for several splicing factor binding motifs.

35 n and subclass-enriched transcription factor binding motifs.

36 t DNA repair proteins that contain ubiquitin-binding motifs.

37 inding of SMAD1/5 and a requirement for SMAD binding motifs.

38 inder threshold followed by a list of glycan-binding motifs.

39 ignificantly with other transcription factor binding motifs.

40 eins featured, length distributions, and HLA-binding motifs.

41 ed by adding either dimerization or membrane-binding motifs.

42 many TGF-beta1-responsive genes possess p53 binding motifs.

43 clin F via their conserved N-terminal cyclin binding motifs.

44 within coding regions near known amoxicillin binding motifs.

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

46 exes and transcription factors competing for binding motifs.

47 enriched for hypoxia-inducible factor family binding motifs.

48 h, revealed significant changes only for RNA-binding motif 3 (Rbm3).

49 in their overall architecture and phosphate binding motif, a lack of sequence identity and some fund

50 s all possess two spatially separated nickel-binding motifs: a variable C-terminal histidine tail and

51 periment, viz., the recoverability of the TF binding motif, accuracy of TF-DNA binding detection, the

52 ecific as well as common features of peptide binding motifs across species.

53 protein/transcriptional coactivator with PDZ-binding motif activation/expression, dedifferentiation,

54 bstantially following injury to reveal STAT3 binding motifs adjacent to genes that regulate essential

55 and physiological studies identify a lipid A-binding motif along the periplasmic leaflet of the inner

56 n each species to evolve hundreds of de novo binding motifs along the neo-X, including expansions of

57 ively charged residues adjacent to the lipid binding motif also resulted in autophagy inhibition, sug

58 host protein Keap1, MLAV VP24 lacks a Keap1-binding motif and fails to activate this cytoprotective

59 n of the E3 ligase complex, such as the zinc-binding motif and N- and C-terminal regions of the prote

60 ncluding expression quantitative trait loci, binding motif and transcriptome analyses, and biological

61 explain the immunodominance of the receptor-binding motif and will guide the design of COVID-19 vacc

62 d mixture model for monomeric and dimeric TF-binding motifs and an expectation maximization algorithm

63 h to model nonlinear interactions between TF binding motifs and chromatin accessibility information u

64 n improved technology for discovering HLA-II binding motifs and conducted a comprehensive analysis of

65 in accessibility surrounding IRF4 and BLIMP1 binding motifs and epigenetic remodeling of IL21R and PR

66 Integrating the binding motifs and expression patterns of RNA binding pr

67 NA sequences containing their respective DNA-binding motifs and identify preferential motif arrangeme

68 vestigate the effect of transcription factor binding motifs and local sequence context on p53-bound C

69 t contain at least one of the 25 specific TF binding motifs and located near bovidae-to-cattle lineag

70 , such as combinatorial transcription factor binding motifs and long non-coding RNAs, that potentiall

71 phosphorylation in cells suggest that kinase binding motifs and phosphorylation sites line up to maxi

72 ched in PHYTOCHROME-INTERACTING FACTOR (PIF)-binding motifs and the transcriptome of pp7l-1 resembled

73 through suramin binding to the "AT-hook" DNA-binding motifs and therefore preventing HMGA2 from bindi

74 Acetylation of mutp53(R158G) alters DNA binding motifs and upregulates TRAIP, a RING domain-cont

75 splicing factor, zinc finger CCCH-type, RNA binding motif, and Ser/Arg rich 2/Rough endosperm 3 (RGH

76 ociates with Flamingo via its C-terminal PDZ binding motif, and we show that Snx27 is essential for n

77 nome-wide, at predicted transcription factor binding motifs, and across human epigenomic domains.

78 modynamic basis for different linker histone binding motifs, and details their physical and chemical

79 R, pS118-ER sites were enriched in GRHL2 DNA binding motifs, and estrogen treatment increased GRHL2 r

80 ionally essential activator protein 1 (AP-1)-binding motifs, and responds to injury, but it cannot re

81 H1 and EZH2 restricted accessibility to AP-1-binding motifs, and their absence promoted a regulatory

82 to the identification of two major receptor-binding motif antigenic sites.

83 type cytochromes with a contracted CXCH heme-binding motif are present throughout the bacterial and a

84 ndom copolymers containing dipicolylamine as binding motifs are designed to coordinate type-3 Cu site

85 ngaged in none, and the intracellular GTPase-binding motifs are essential for trajectory choice and s

86 genome-wide analyses showing that their DNA-binding motifs are highly overrepresented in regions tha

87 ATF4 binding motifs are identified in multiple clock genes, i

88 However, weakly associated binding motifs are often difficult to characterize.

89 lation of PMP22 nor its putative cholesterol binding motifs are required for this preference.

90 Two almost isoenergetic electron binding motifs are seen for cluster sizes 20 <= n <= 40,

91 fic classes of CTCF and transcription factor binding motifs are similarly correlated with ASM in canc

92 These new polymer materials and binding motifs are sufficient to bear normal and shear s

93 nd TAZ (transcriptional coactivator with PDZ-binding motif) are regulators of single-cell volume.

94 gically inspired hydroxamate groups and zinc-binding motifs assembles through concurrent Fe(3+) and Z

95 set of 25 specific transcription factor (TF) binding motifs associated with recently active TEs.

96 , zonula occludens-1 protein (PDZ) consensus binding motif at its C-terminus and binds to PDZ domain

97 on, CRISPRi/dCas9-mediated blocking of Ash2l-binding motifs at these super-enhancers also prevents OS

98 ch repair protein MutL has an internal clamp-binding motif, but its interaction with the beta-clamp h

99 The Scap-binding motif, but not the degradation signal, is conser

100 t the ligands still bind at the noncanonical binding motif, but with fewer hydrogen-bonding interacti

101 n their dimeric assembly consists of two Plg binding motifs (called the a1 and a2 repeats).

102 he absence of any sequence similarity to the binding motif, can DNA shape still increase binding prob

103 signal, conferred by low affinity pMad/Medea binding motifs, can contribute to the specification of B

104 l-induced" pocket and possess bicyclic hinge-binding motifs capable of forming more than one hydrogen

105 on to the genome-wide accessibility of their binding motifs classifies them as predominantly openers

106 ome analysis revealed a distinct DQ6 peptide-binding motif compared with the susceptible DQ2/8 molecu

107 l of these proteins contain the typical heme-binding motif CXXCH and require the Ccm proteins for mat

108 peptide mimetic derived from the Na(V)1.8 WW binding motif decreased sodium currents, reduced Na(V)1.

109 ular-specific, low-affinity, 'divergent' Gli-binding motifs (dGBMs).

110 lyMDB provides data visualization and glycan-binding motif discovery for 5203 glycan microarray sampl

111 tivated transcriptional coactivator with PDZ-binding motif-driven GBM mouse model, neutrophils coinci

112 lial permeability without MLC-P via an actin-binding motif, DVRGLL.

113 but cannot describe how proteins with clamp-binding motifs embedded in structured domains are recogn

114 (ROK) family, but many lack the canonical Zn-binding motif expected for this function, and the sugar-

115 o PSD-95 was very weak, and deleting the PDZ-binding motif failed to alter synaptic trafficking.

116 We show that a single binding motif for a key regulatory transcription factor

117 intracellular N terminus, which contains the binding motif for endogenous Src tyrosine kinase that co

118 confirmed by the identification of a YYIYVI-binding motif for HSC70 that spans residues 83-88 of the

119 ession and identified a transcription factor binding motif for LRF near these modifications in both c

120 eIF2D requires its RNA-binding motif for regulation of 5' leader-mediated ATF4

121 demonstrate that E2F1 acetylation creates a binding motif for the bromodomains of the p300/KAT3B and

122 We found that the binding motif for the RNA-binding proteins Pumilio 1 and

123 te assembly uncovered a transcription factor-binding motif for ZNF263, a C2H2 zinc finger protein.

124 t the associated genetic loci resided within binding motifs for adipogenic transcription factors (e.g

125 tes are significantly enriched for predicted binding motifs for critical epidermal transcription fact

126 ncluding a mouse-specific gene set, and bear binding motifs for critical regulators of spermatogenesi

127 aries, we identified and refined the peptide binding motifs for each of the four molecules and found

128 associated with chromatin sites that harbor binding motifs for IKAROS and EBF1 and physically associ

129 TAC") does so by rediscovering ab initio the binding motifs for known regulators and some unknown one

130 ytes compared to wild type were enriched for binding motifs for NF-kappaB and AP-1, transcription fac

131 oxp3 targets depended on the presence of DNA binding motifs for other TFs, including TCF1.

132 Binding motifs for RUNX and other hematopoietic transcri

133 required distinct transcription factor (TF) binding motifs for their accessibility.

134 charged cleft and a helix-hairpin-helix DNA-binding motif found in other DNA repair enzymes.

135 hat remodel the canonical magnesium (Mg(2+))-binding motif found in terpene cyclases.

136 LOP against other MEA methods in identifying binding motifs found enriched in differentially active r

137 oves the ability to call enrichment of ISGF3 binding motifs from differential acetylation ChIP-seq da

138 ic clusters, and enhanceosomes, from real TF binding motifs from diverse TF families.

139 ethods when quantifying the enrichment of TF binding motifs from ENCODE TF ChIP-seq datasets.

140 lytic motif (DPP(Y/F)) as well as the AdoMet-binding motif (FXGXG) by site-directed mutagenesis aboli

141 N-(4-(p-methoxyphenyl)butanoyl)-Gly albumin-binding motifs generated HTK03121 and HTK03123, respecti

142 The selective enrichment of the DNA binding motif GRHL2 in the breast cancer-specific ER cis

143 hin a high-affinity integrin alpha(2)beta(1)-binding motif, GROGER.

144 Several nSH3-binding motifs have been identified in the SOS1 PR domai

145 an SAC, since the relevant PLK1 and PP2A-B56 binding motifs have coevolved in the same region on MADB

146 MD1 requires Fe(II) and the integrity of its binding motif His-X-Asp, which is conserved in Fe-depend

147 thermore, two important transcription factor-binding motifs, hypoxia-inducible factor 2alpha (HIF2alp

148 predict that a few residues on the receptor-binding motif, i.e., 452, 489, 500, 501, and 505, have h

149 most frequently mutated ETS, AP-1, and NF-kB binding motifs, implicating these motifs as governors of

150 coviruses detected to date, and its receptor-binding motif, important for specificity to human ACE2 r

151 2 interacts with HP1 through a conserved HP1-binding motif in its N-terminus, which in turn leads to

152 o investigate the contribution of this STAT1-binding motif in NiV-mediated disease, we produced rNiVs

153 otif C, which has been indicated as a cyclin binding motif in other contexts, appears to be relativel

154 We identified a potential SP6 binding motif in the AMBN proximal promoter sequence and

155 we identified a putative EF-hand-like Ca(2+) binding motif in the carboxyl terminal region of BTV non

156 We identified a consensus glycosphingolipid-binding motif in the extracellular juxtamembrane domain

157 Phosphorylation of the ankyrin binding motif in the L1 cytoplasmic domain was studied a

158 tations to the S-adenosyl-l-methionine (SAM) binding motif in the nsp14 abolished the G-N-7 MTase act

159 niques to confirm the predicted Walker-B ATP-binding motif in the phage lambda motor and to investiga

160 through YAP association with the TEA domain-binding motif in the promoter region of inflammatory cyt

161 We also describe a novel Ubiquitin binding motif in the targeted region as part of the iden

162 g a conserved cysteine within a 3His/1Cys Zn-binding motif in TlpD that inactivates the chemotransduc

163 MEA method that determines enrichment of TF binding motifs in a list of scored regulatory regions, w

164 ion factors and displayed enrichment of NR4A-binding motifs in accessible chromatin regions.

165 minating model for transcription factor (TF)-binding motifs in DNA.

166 lf4; reflecting a genome-wide paucity in ETS-binding motifs in Etv6 genomic targets, Klf4 then recrui

167 ntification and visualization of upstream TF binding motifs in InDel-containing enhancers.

168 tool to analyze paired transcription factor binding motifs in the promoters of cell type-specific ge

169 egulated genes preferentially contained NF-Y-binding motifs in their proximal promoters, and notably

170 However, presence of the Cu-binding motifs in these proteins raised the possibility

171 tructure by NMR identified a linear c-di-GMP-binding motif, in which a self-intercalated c-di-GMP dim

172 ighly concordant set of transcription factor binding motifs, including motifs for the GC receptor cof

173 the presence of several transcription factor binding motifs, including RBPJ1, EGR1, and SOX4, suggest

174 n or disruption of TF (transcription factor)-binding motifs, inferred from alternative alleles at the

175 ucture revealed an EF domain with two Ca(2+)-binding motifs inserted within the catalytic domain.

176 revealed that thyroid hormone receptor 1beta-binding motif insertions have evolved in several genera

177 halamic T(3), driven in part by the receptor-binding motif insertions in some cricetid genomes, contr

178 within the regulatory domain, only the clamp binding motif is required for the interaction between th

179 We conclude that diversification in DNA-binding motifs is pervasive, and present a new tool and

180 along with the presence of a catalytic zinc-binding motif, it is possible that the identified protei

181 onstrate that the XLF tail along with the Ku-binding motif (KBM) at the extreme C-terminus are requir

182 Recently, the first PP2A:B56 consensus binding motif, LxxIxE, was identified.

183 howed that mutation of one of its 2 putative binding motifs markedly diminished T cell activation aft

184 le two classes of extra-terminal (ET)-domain binding motifs mediate acetylation-independent interacti

185 ated SF1 sites and potentially rescuing GATA binding motifs might play a role in the development of P

186 s were identified that interact with the PDZ-binding motif of Claudin-2 in liver metastatic breast ca

187 We now demonstrate that the PDZ-binding motif of Claudin-2 is necessary for anchorage-in

188 udin-2, an interaction that requires the PDZ-binding motif of Claudin-2.

189 diated phosphorylation of the C-terminal PDZ-binding motif of delta-catenin.

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

191 As the N-lobe binding motif of Na(V)1.5 is a mutational hotspot for in

192 conformation of the minimal pseudo-dipeptide binding motif of pepstatin A, a microbial oligopeptide i

193 n of tyrosine-1229 (L1-Y1229) at the ankyrin binding motif of the L1 cytoplasmic domain, leading to t

194 ous mutations to the common N-terminal STAT1-binding motif of the NiV P, V, and W proteins affected t

195 Here, we identified a novel DNA-binding motif of ZEBRA, N terminal to the canonical bZIP

196 understand ANT1 functions, we determined the binding motif of ZmANT1 and then showed that ZmANT1 bind

197 e strongly enriched for transcription-factor-binding motifs of AP-1 family members.

198 vivax strain transcending and targeted known binding motifs of DBPII with DARC.

199 hat O-glycans positioned within the receptor binding motifs of members of the neuropeptide Y and gluc

200 mediated interaction with the C-terminal PDZ-binding motifs of protein cargos.

201 hromatin remodeling in regions enriched with binding motifs of the pioneer transcription factor PU.1.

202 Finally, we demonstrate that the nucleotide-binding motifs of the predicted atypical kinase Mcp2 are

203 The similar DNA-binding motifs of the various HOX TFs contrast with the

204 rmore, tissue-specific NFR were enriched for binding motifs of transcription factors related to tissu

205 ognate protein 70 (HSC70) and its KFERQ-like binding motif on substrate proteins.

206 f the major myeloid integrin alpha(M)beta(2)-binding motif on the gamma chain of fibrin(ogen).

207 or 6 (GATA-6) and NF-kappaB to their cognate binding motifs on CAV1, CAV2, and CAV3 promoters in obst

208 oacervate to deliver IL-12, in which heparin-binding motifs on IL-12 allow for its effective encapsul

209 The portability of the binding motif opens avenues for the engineering of semis

210 ed rNiVs with complete deletion of the STAT1-binding motif or the Y116E mutation for ferret challenge

211 may introduce aberrant transcription factor binding motifs or enhancer hijacking by structural varia

212 ive alleles altered the transcription factor binding motifs or histone modifications, indicating the

213 cycling of ligands encompassing the SBM, PDZ-binding motif, or both motifs.

214 ng the flexibility of the linker between two binding motifs, our results suggest that the conformatio

215 information about transcription factor (TF) binding motifs, patterns of covalent histone modificatio

216 The PDZ binding motif (PBM) and an Arg-rich motif upstream of PB

217 DAPLE contains a PDZ-binding motif (PBM) and is also mutated in human NSCH, s

218 d PDZ domain and a highly conserved aPKC PDZ-binding motif (PBM) that is required in the context of t

219 The C-terminal PDZ-binding motif (PDZbm) in OTULIN associates with the carg

220 te latch (PSL), resembles the consensus COP1-binding motif present in known COP1 substrates.

221 Replacement of the imidazopyridine hinge binding motif present in the initial compounds of this s

222 ays showed that NKX2.1 binds in vitro to NKX binding motifs present in the neuronal Pomc enhancers nP

223 RNA-binding motif protein 10 (RBM10) is an RNA-binding prote

224 negatively regulating ERV expression was RNA-binding motif protein 4 (RBM4).

225 We found that the maize (Zea mays) RNA binding motif protein 48 (RBM48) is a U12 splicing facto

226 how that following genotoxic stress, the RNA-binding motif protein 7 (RBM7) stimulates RNA polymerase

227 unprecedented finding that the conserved RNA-binding motif protein, RBM24, positively controls Sox2 m

228 ng the pathogenic R636S variant of human RNA-binding motif protein-20 (RBM20), we discovered that RNP

229 e that overlaps with the human ACE2 receptor binding motif providing a structural basis for its neutr

230 he nSH3/cSH3 domains have distinct preferred binding motifs: PxxPxR for nSH3 and PxxxRxxKP for cSH3 (

231 nce of 2019-nCoV RBD, including its receptor-binding motif (RBM) that directly contacts ACE2, is simi

232 Despite lacking a known RNA-binding motif, recombinant UIEF1 interacted with RNA, an

233 48, adjacent to the canonical phiX(D/E) Cul3-binding motif, reduced affinity of A55BB for Cul3-NTD by

234 tide (SBP), contains two potential sulfatide-binding motifs represented by two consecutive polybasic

235 of the light-harvesting complex chlorophyll-binding motif required for chlorophyll binding were muta

236 scription Factors (TFs) to their cognate DNA binding motifs requires a precise control over nucleosom

237 tochore through its HFD and N-terminal Ndc80-binding motif, respectively.

238 serine proteases, its carboxy-terminal CARD-binding motif restrained the activation of pro-caspase-1

239 cs (iTRAQ) and an in silico analysis of SigF binding motifs revealed possible targets/pathways under

240 r SNX6 and a bipartite motif, termed SNX-BAR-binding motif (SBM), in the cargoes.

241 HLA-DP peptide-binding motifs showed a clear association with the HLA-D

242 hat CoV-2 RBD does not bind to ACE2 with the binding motif shown in experiments, but it rotates becau

243 We show that the microtubule-binding motif spans two positively charged patches compr

244 ompete identifies a GC-rich region as SERBP1-binding motif; subsequent genomic and functional analyse

245 f GPCRs contain at least one putative 14-3-3 binding motif, suggesting GPCR/14-3-3 association could

246 SAGA1 contains a starch binding motif, suggesting that it may directly regulate

247 egions were enriched in transcription factor binding motifs, suggesting a potential gene regulatory r

248 1 proteins also carry multiple "AT-hook" DNA-binding motifs, suramin is expected to inhibit HMGA1-DNA

249 n (YAP)/Transcriptional coactivator with PDZ-binding motif (TAZ) activation.

250 P) and transcriptional co-activator with PDZ-binding motif (TAZ) are increased in many human cancers,

251 homolog transcriptional coactivator with PDZ-binding motif (TAZ) are key effectors of the Hippo pathw

252 AP) and transcriptional coactivator with PDZ-binding motif (TAZ) are the key mediators of the Hippo s

253 AP) and transcriptional coactivator with PDZ-binding motif (TAZ) in hepatocytes to facilitate cell-ce

254 sociated protein (YAP) and its paralogue PDZ-binding motif (TAZ) with associated decline in activatio

255 AP) and transcriptional coactivator with PDZ-binding motif (TAZ), the key downstream transcriptional

256 ap) and transcriptional coactivator with PDZ-binding motif (Taz), two transcriptional coactivators kn

257 (YAP1)/transcriptional coactivator with PDZ binding motif (TAZ)-dependent, irreversible fibrosis and

258 tion of transcriptional coactivator with PDZ-binding motif (TAZ).

259 AP) and transcriptional coactivator with PDZ-binding motif (TAZ).

260 AP) and transcriptional coactivator with PDZ-binding motif (TAZ).

261 AP) and transcriptional coactivator with PDZ-binding motif (TAZ, also called WWTR1), the main downstr

262 aiP exposes a mimic of an eukaryotic ATG16L1-binding motif that binds to ATG16L1's WD40 domain.

263 , Frizzled4, which contains a C-terminal PDZ-binding motif that can bind to Dlg1 PDZ domains, appears

264 that the WD40 domain of FBXW7 is a novel PAR-binding motif that facilitates early recruitment of FBXW

265 d C-terminal tail of NHERF1 has a type 1 PDZ-binding motif that interacts weakly with the proximal, s

266 with the beta-clamp harbor a conserved clamp-binding motif that is often found in extended regions.

267 cysteine and histidine residues form a zinc-binding motif that is required for HBx function.IMPORTAN

268 Mutational analyses identified a FxxxLxxxK binding motif that is shared by VpdB and SidH, but not b

269 trafficking and signaling, and provide a WDD-binding motif that might be used to identify additional

270 ortantly, we show that the CArG-box-like DNA-binding motifs that are bound by PHE1 have been distribu

271 e three molecules in the system contains two binding motifs that can interact with each other and are

272 roughly characterize a general PP4 consensus-binding motif, the FxxP motif.

273 Driven by a distortion of the ligand-binding motifs, the presence of hydroxyl species changes

274 affect RNA-protein interactions from outside binding motifs through altered RNA secondary structure.

275 Genetic elimination of the fibrinogen binding motif to CD11b reduced neuroinflammation, synapt

276 ikely interacts with Aer2 via conserved CheD-binding motifs to make Aer2 a better methylation substra

277 tions of A20's zinc finger 7 (ZF7) ubiquitin-binding motif uniformly developed digit arthritis with f

278 o steric immobilization of the proximal heme-binding motifs upon complex formation, a finding that ma

279 protein/transcriptional coactivator with PDZ-binding motif via rho kinase, which were shown to increa

280 We identified putative ATP-binding motifs (Walker-A and Walker-B) in each of the AT

281 n-regulated by ethylene in shoots, and a DNA binding motif was identified that is important for this

282 eCh CAB domain with a functional chlorophyll-binding motif was retained in all currently known cyanob

283 as enriched in multiple transcription factor binding motifs, was bound by an important transcription

284 chelators with the PSMA-specific urea-based binding motif were developed.

285 -binding domain nor the clathrin heavy chain-binding motif were needed for virus infection, whereas t

286 FrtR protein was purified, and conserved DNA binding motifs were determined using electrophoretic mob

287 profiled >40 HLA-II alleles and showed that binding motifs were highly sensitive to HLA-DM, a peptid

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

289 minal domain (CT) of GluD1 has a classic PDZ-binding motif, which is critical for the synaptic traffi

290 rring contracted Cys-Lys-Cys-His (CKCH) heme-binding motif, which is encoded in the hydrazine synthas

291 n, we also identified differences in peptide binding motifs, which could explain the observed variati

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

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

294 We identified an extended gyrase binding motif with phased 10-bp G/C content variation, i

295 ized in DPC-2 shared certain similar peptide-binding motifs with DPC-1 or DPC-3 alleles, but signific

296 at can act as a template to display multiple binding motifs with precise spatial pattern-recognition

297 Structural analyses revealed an EB-like +TIP-binding motif within the capsid major homology region (M

298 l analysis reveals that ppGpp binds the PRPP binding motif within the XPRT active site.

299 alter RBP-RNA interactions by modifying RBP binding motifs within RNA.

300 near motif known as the zDHHC ankyrin repeat-binding motif (zDABM) in SNAP25 ((112)VVASQP(117)), whic