ライフサイエンスコーパス: binding motif

1 ontaining aromatic amino acids, the caveolin-binding motif.

2 use the predicted protein contains a Myb DNA binding motif.

3 846053 affects a putative intronic NFAT5 DNA binding motif.

4 e tandem Tudor domain and masks its H4K20me2 binding motif.

5 lation site and flanks the hydrophobic Ezrin-binding motif.

6 ly potent inhibitors having a sulfamide zinc-binding motif.

7 xtended tail domain with an additional actin-binding motif.

8 ia by a mechanism of action using a lipid-II-binding motif.

9 were strongly enriched for the consensus GR-binding motif.

10 ged preference for a low-affinity, secondary binding motif.

11 natal thymic epithelia and defined the Foxn1 binding motif.

12 group via an aromatic box, a typical choline-binding motif.

13 but also afforded discovery of a novel CTCF binding motif.

14 a novel small ubiquitin-like modifier (SUMO) binding motif.

15 e allelic imbalance from the disruption of a binding motif.

16 alf and PIFs' conserved active-phytochrome B binding motif.

17 binding sites, based on the discovery of its binding motif.

18 dominantly at W-box elements, the known WRKY binding motif.

19 4 E3 ligase requires a highly conserved zinc-binding motif.

20 inding through an Arg-Gly-Asp (RGD) integrin-binding motif.

21 s by a single point mutation in the caveolin-binding motif.

22 imately 800) with no high-throughput-derived binding motifs.

23 fic domain and Kv7 channel 1-5-10 calmodulin-binding motifs.

24 enhancers do not encode canonical NF-kappaB binding motifs.

25 f Clostridium difficile has intact LytM zinc-binding motifs.

26 shoot compared with models based on known TF binding motifs.

27 ated R domain contains nine different 14-3-3 binding motifs.

28 fluorescent proteins (FPs) fused with Zn(2+)-binding motifs.

29 ndidate binding sites and discover potential binding motifs.

30 binding was obtained at two canonical STAT5 binding motifs.

31 ociate with STAT5 at sites lacking bona fide binding motifs.

32 Gli3 has multiple weak SPOP binding motifs.

33 ol for characterizing CB1R allosteric ligand-binding motifs.

34 sting the existence of common RGD-containing binding motifs.

35 ctly alter recognizable transcription factor binding motifs.

36 o accurately infer monomeric and homodimeric binding motifs.

37 on inadequate knowledge of cell-specific DNA binding motifs.

38 helices were replaced by synthetic membrane-binding motifs.

39 key residue difference in the consensus GTP-binding motifs.

40 n with the DNA minor groove that flanks PU.1-binding motifs.

41 odifiers that bind RNA without canonical RNA-binding motifs.

42 be related to their different C-terminal PDZ binding motifs.

43 istinct combinations of transcription factor-binding motifs.

44 , we showed that several residues in the RNA-binding motif 2 interact with the N-terminal region of t

45 ruption of the implicated intramolecular RNA-binding motif 2-RS domain interaction impairs both the d

46 The splicing factor RNA-binding motif 20 (RBM20) regulates the contour length of

47 NA recognition motif (RRM) of one of the RNA binding motif-20 alleles was floxed and that expressed t

48 Inhibition of the RNA binding motif-20-based titin splicing system upregulates

49 hrough inhibition of the splicing factor RNA binding motif-20.

50 ific binding of the three proteins to an Rsm-binding motif (5'CANGGANG3') encompassing the translatio

51 tivity, and an extended tail with tail actin-binding motif, allow it to play an important role in sta

52 e, TRPC4/5 channels contain a C-terminal PDZ-binding motif allowing for binding of the scaffolding pr

53 ed flat free energy landscape containing all binding motifs allows determination of the ligand mechan

54 Strikingly, these c-di-GMP-binding motifs also stabilize an open state conformation

55 Transcription factor binding motif analysis showed an increased activity of p

56 Moreover, DNA-binding motif analysis within the SE segments suggest th

57 flanked by a C-terminal helix-turn-helix DNA-binding motif and a divergent N-terminal receiver domain

58 tes with Rad18 directly via a consensus USP7-binding motif and can disassemble Rad18-dependent poly-u

59 uted cyclopentyl amide as a preferred FKBP51-binding motif and elucidated its binding mode to provide

60 We have identified an hnRNP E1 consensus-binding motif and genomically resolved a subset of genes

61 erizes the binding kinetics of the consensus-binding motif and hnRNP E1, its various K-homology (KH)

62 enetic variation that disrupts the consensus binding motif and its methylation is often associated wi

63 rotective effect of EphB2 depends on its PDZ-binding motif and the presence of neuronal activity but

64 To elucidate the CB1R allosteric binding motif and thereby facilitate rational drug disco

65 se data enabled the discovery of subdominant binding motifs and an integrative analysis quantifying t

66 , we identify that PrimPol possesses two RPA-binding motifs and ascertained the key residues required

67 evolution," to reflect the diversity of both binding motifs and binding motif transitions and the fac

68 ractions is crucial to understanding protein binding motifs and cellular function, that is, an intera

69 referentially in the direct vicinity of NFAT-binding motifs and in a distinct orientation to them.

70 the availability of large scale data for RBP binding motifs and in vivo binding sites results in the

71 inding, burst-like expression, degeneracy of binding motifs and massive regulatory rewiring during ev

72 ry data (e.g. presence/absence of mutations, binding, motifs and epigenetic marks) and continuous dat

73 mbrane protein that contains the WD40 domain-binding motif, and disrupts its normal intracellular tra

74 in the identification of seven novel Mg(2+)-binding motifs, and all RNA structures in the PDB were s

75 g sites within enhancers containing multiple binding motifs, and allows for the analysis of in vivo b

76 e virus were enriched for HLA class I and II binding motifs, and constituted both species-specific (R

77 ription factors relevant to the CRM or their binding motifs, and is thus more widely applicable than

78 in vivo, identifies export-promoting ALYREF-binding motifs, and reveals CstF64- and PABPN1-mediated

79 to intragenic regions, enriched for Myc DNA binding motifs, and showed Myc binding.

80 ion in the acetyllysine binding site, common binding motifs, and unusual interactions (e.g., the repl

81 he conserved residues in the putative cyclin-binding motif are important for protein expression, prot

82 t existing analysis methods require that the binding motifs are enriched in the population relative t

83 C terminus of VP1, a position where integrin binding motifs are found in some other picornaviruses.

84 we find that particular transcription factor binding motifs are intrinsically biased toward the gener

85 Unlike ETS-mediated regulation, MEF2-binding motifs are not ubiquitous to all endothelial gen

86 t the notion that the distinct alignments in binding motifs are part of a critical regulatory strateg

87 Akt (RxRxxSF) and PDK1 (RFxFPxFS) binding motifs are present in hBVR.

88 rtance of regulatory syntax, as noncanonical binding motifs are typically disregarded by enhancer det

89 gnition patterns, as well as the protein-RNA binding motifs, are then identified and analyzed.

90 midazoles with a rigidized 7-azaindole hinge binding motif as a new structural class of EGFR inhibito

91 nd Taz (transcriptional coactivator with PDZ-binding motif), as key steps in oncogenesis.

92 In a similar way, deletion of the Par3-binding motif at the C-terminus of VE-cadherin impairs a

93 P hydrolysis in the presence of specific RNA binding motifs (AUUUA) of cyclin D1 mRNA.

94 of stem-loops that each present a minimal CP-binding motif AXXA in the loops.

95 eveloped efficient algorithms for estimating binding motifs based on HT-SELEX data.

96 Despite the divergence of their binding motifs, both mouse DUX and human DUX4 in mouse a

97 e ACGT motif (Box2) rather than by the G-Box binding motif (Box1) in the vegetative phase of developm

98 but not of a variant lacking the periplakin binding motif, BTN3A1Deltaexon5, restored gammadelta T c

99 s motor domain contains conserved nucleotide binding motifs, but is divergent in sequence ( 35% ident

100 f the flexible linker and the intramolecular binding motif by assuming the flexible linker behaves as

101 ariant lies within the consensus SH3 protein-binding motif by which SHANK2 may interact with post-syn

102 demonstrate that local transcription factor binding motifs can be identified from a network trained

103 This CKK binding motif (CBM) is adjacent to the domain that inter

104 Two SRSF3-binding motifs, CCAGC(G)C and A(G)CAGCA, are enriched to

105 n structure analysis, further reveal how HLA-binding motifs change with peptide length and predict ne

106 Isolated deletions of the canonical GATA1 binding motif completely abrogated binding of the cofact

107 A single-pass TM protein with one PDZ binding motif concentrated in the synapse as do AMPARs y

108 threonine for alanine in the C-terminal PDZ-binding motif conferred DAG sensitivity to the channel.

109 re, bioinformatics data, showing key citrate-binding motifs conserved across a broad range of PNPase

110 XI binding, which identified a series of FXI binding motifs containing the signature Asp-Phe-Pro (DFP

111 base pair (bp) deletion within IQ calmodulin-binding motif-containing protein-1 (IQCB1), the gene tha

112 ow how macromolecular components outside the binding motif contribute to integrin recognition.

113 he presence of transcription factor (TF) DNA binding motifs correlated with specific TF activity duri

114 Some of the key fluoride-binding motifs covered in this review include the triflu

115 rylation of a serine in the winged helix DNA binding motif curtails FoxO1 nucleosome binding.

116 ng nascent transcript RNA-seq, ChIP-seq, and binding motif datasets from lipid A-stimulated macrophag

117 Furthermore, removal of CFTR's PDZ binding motif (DeltaTRL) prevented actin rearrangement,

118 oma and glioblastoma cell lines in a PDZ.PDZ binding motifs-dependent manner, but the cellular partne

119 Three type-B ARR DNA-binding motifs, determined by use of protein-binding mic

120 was tested, but mutation of the putative SH3 binding motif did not affect transformation.

121 The conformation of the prodomain integrin-binding motif differs in the presence and absence of int

122 t, despite the presence of putative cytokine-binding motifs, does not detectably interact with pathwa

123 s containing one or more double-stranded RNA binding motif (dsRBM) that play important roles in small

124 uring a tandem array of two highly conserved binding motifs, each comprising a 24-residue sequence RL

125 on, we show that a peptide comprising the ET binding motif (EBM) of MLV IN can disrupt the cognate in

126 scriptomic profiles and transcription factor binding motifs enabled us to construct a regulatory netw

127 Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 mu

128 ction of spinophilin with the C-terminal PDZ binding motif encoded by Group I mGluRs.

129 ion pattern, identified transcription factor binding motifs enriched in each cluster, and generated a

130 e the interplay between transcription factor binding motif evolution and GRN topology.

131 owed that D145:H148 followed a general metal binding motif favored by Cd(II).

132 rts binding to the phosphorylated FHA domain binding motifs (FBMs) in XRCC1 and XRCC4.

133 gen residues gamma390-396 comprise the major binding motif for FXIII-A2B2 Compared with gammaA/gammaA

134 he T to C transition in rs429358 generates a binding motif for nuclear respiratory factor NRF1.

135 l cases are predicted to disrupt a canonical binding motif for the hematopoietic transcription factor

136 ripts contain a disproportionate amount of a binding motif for the quaking RNA binding protein, a seq

137 e identify and experimentally define a novel binding motif for the SOS transcriptional repressor LexA

138 ces for HLA-C*06:02 that defines the peptide-binding motif for this HLA allomorph.

139 and identified DxxxxE as a potential Mg(2+)-binding motif for type II DTSs of bacterial origin.

140 ividual (3-14) and the lack of clear peptide binding motifs for class II molecules.

141 dvance, the utilization of the corresponding binding motifs for fast and robust quantitative chemosen

142 gions are enriched for clusters of consensus binding motifs for HOX, PBX, and MEIS, and many display

143 hromatin regions, which demonstrate enriched binding motifs for inducible factors and correlate with

144 associated peaks were enriched for consensus binding motifs for NKX2-1, LHX, and SOX transcription fa

145 n, characterized by enrichment for consensus binding motifs for Nr4a and NFAT transcription factors.

146 , our computational analysis discovered that binding motifs for RUNX and CREB1 are found preferential

147 These mRNAs' 3'UTRs have enriched binding motifs for several RNA-binding proteins, which i

148 Pmp22 enhancers contain binding motifs for TEA domain (Tead) transcription facto

149 s characterized by a precise organization of binding motifs for the Sertoli cell reprogramming factor

150 reast and endometrial cancer and enriched in binding motifs for the transcription factor FOXA1, which

151 Demethylation occurred first at binding motifs for the transcription factors NF-kappaB a

152 anscription factors (TFs), and enrichment of binding motifs for these TFs in alphaTC1/betaTC6 cis-reg

153 lysis of SAMHD1 identifies a putative cyclin-binding motif found in many cyclin-CDK complex substrate

154 The Patescibacteria LexA-binding motif has unusual direct-repeat structure, and c

155 core of MbIV resembles the tetrapeptide HCF-binding motif (HBM) found in many HCF-interaction partne

156 vitro evolution identify consensus hnRNP A1 binding motifs; however, such data do not reveal how sur

157 egulon is enriched for highly conserved CcpA binding motifs (i.e. cre sites).

158 ivities were more likely to enrich for miRNA binding motifs; (iii) expression levels of these genes a

159 We identified a conserved SHR-binding motif in 13 BIRD/IDD transcription factors.

160 kidney, via PDLIM5's PDZ domain and the PDZ binding motif in AE1C.

161 e variants or deletion of the C-terminal PDZ-binding motif in CaV1.3L induced aberrant dendritic spin

162 e M18BP1 motif resembles a CENP-A nucleosome binding motif in CENP-C, and we show that CENP-C compete

163 on of the glycosyltransferase-like metal ion binding motif in H3 greatly diminished its binding to UD

164 loop-helix domain and a novel 15-residue MYC-binding motif in MKK3 (MBM).

165 mmary, we have identified a unique substrate-binding motif in NleE and OspZ that is required for the

166 The Ctf19-Mcm21 binding motif in Okp1 configures a branch of mitotic inn

167 NHERF1 interacts with the PDZ-binding motif in PMCA2 in both normal and malignant brea

168 DE genes with a NKD binding motif in the 5' promoter region were considered

169 We mutagenized a conserved CCTSE metal-binding motif in the domain and assessed the impact of t

170 We identify a Lys-Gly-Glu (KGE) integrin-binding motif in the FVIIa protease domain that is requi

171 , the absence of a conserved ephrin receptor-binding motif in the MojV attachment glycoprotein (MojV-

172 and D/NxSxxG) and a newly described c-di-GMP-binding motif in the MrkH N domain.

173 II (CaMKII) strongly interacts with a novel binding motif in the N-terminal domain of CaV1 LTCC alph

174 d affinity of the holo-DnrF for its specific binding motif in the napD promoter.

175 lex' (2:2:4), using a previously undescribed binding motif in the Unc5D TSP1 domain.

176 Mutating the Pals1-binding motif in VE-cadherin abrogates the ability of VE

177 ositions nucleosomes on top of adjacent Ume6 binding motifs in a highly predictable and reproducible

178 Finally, by integrating transcription factor binding motifs in a machine learning framework, we ident

179 guidelines for the detection of cholesterol-binding motifs in any membrane protein.

180 ese echinoderms and that the targets and the binding motifs in associated cis-regulatory sequences ar

181 Here we show that two Cdc20-binding motifs in BubR1 of the recently identified ABBA

182 We identified critical NFAT binding motifs in the AQP5 promoter that are involved in

183 sence of numerous putative non-canonical p53 binding motifs in the CerS6 promoter.

184 arch reveals occurrences of protein and drug binding motifs in the HERV RNA ensemble that do not occu

185 nd Taz (transcriptional coactivator with PDZ binding motif) in tissue development, homeostasis, and r

186 evolved under selection pressure to encode a binding motif innately capable of recognizing and neutra

187 rotein, demonstrating that ataxin3's p97/VCP-binding motif interacts with the inter-lobe cleft in the

188 esidues 483 and 484, located within the Alix-binding motif involved in virus budding, as major contri

189 This intramolecular binding motif is connected to the p53 binding domain of

190 A cationic PS-binding motif is identified in this domain, replacement

191 This c-di-GMP-binding motif is present in diverse bacterial proteins e

192 The number of low-affinity binding motifs is significantly depressed in sea urchins

193 TAZ (transcriptional coactivator with PDZ binding motif) is a transcriptional coactivator and end

194 hereas M2, although containing a cholesterol binding motif, is not raft associated.

195 oding an L53F protein variant within the ATP-binding motif, is prioritized as the candidate at the lo

196 partially in agreement with the extended PP1-binding motif K(V/I)FF-X5-8Phi1Phi2-X8-9-R.

197 The Ku-binding motif (KBM) is a short peptide module first iden

198 ) and sodium channels possess homologous CaM-binding motifs, known as IQ motifs in their C termini, w

199 Screening around the minimal ethyl urea binding motif led to the identification of isoquinoline

200 , Oxygen and Voltage sensing 2 (LOV2) flavin-binding motif located within the N-terminus of the photo

201 n a collection of known transcription factor binding motifs, many bioinformatics methods have been pr

202 ed a high-resolution structure of WHAMM's MT-binding motif (MBM) assembling around MTs using cryo-ele

203 diimide (PDI) unit and two triazolium anion-binding motifs, mechanically bonded with two smaller iso

204 e observed that SAMHD1 mutants of the cyclin-binding motif mislocalized to a nuclear compartment and

205 ing conservation of the transcription factor-binding motif (motif-based) are shown to substantially o

206 Furthermore, the RNA-binding motif mutants are defective for their export thr

207 In particular, Vpr zinc-binding motif mutation or TPEN treatment efficiently inh

208 ates specific Sdt isoforms containing a Neur binding motif (NBM).

209 n binding to LRP1 based on the proposed LRP1 binding motif of 2 lysine residues separated by about 21

210 The highly conserved PDZ-binding motif of ABCC4 is required for ABCC4 and MPP1 to

211 red via the BIR3 domain of cIAP1 and the IAP-binding motif of C9b, but did not require proteolytic cl

212 by selectively interacting with a secondary binding motif of CFTR (pS753).

213 A2, which can become associated with the PDZ-binding motif of EphB2 through PDZ domain-containing pro

214 Furthermore, while the first dsRNA-binding motif of Loqs-PD is dispensable for enhancing cl

215 We have characterized the peptide-binding motif of Mamu-A2*05:01, and elucidated the bindi

216 s PDZ domain interacts directly with the PDZ-binding motif of nectin-1.

217 SNX27 binds directly to the C-terminal PDZ-binding motif of PTHR, wiring it to retromer for endosom

218 es an amino acid substitution in the calcium-binding motif of the extracellular cadherin (EC) domains

219 f human POT1 (POT1C) complexed with the POT1-binding motif of TPP1.

220 lity mass spectrometry, clearly indicating a binding motif of two partially overlapping diarylviologe

221 Residues in a conserved zinc-binding motif of Vpx were essential for the recruitment

222 epigenetic network selectively enriched for binding motifs of a transcription factor cohort expresse

223 Variations modifying the consensus binding motifs of IRF4 and CTCF in the XL9 regulatory co

224 Mutations in ATP/GTP binding motifs of SQU and KEW lead to failure of phospho

225 s, and their promoters were enriched for the binding motifs of TFAP2 (which was identified in promote

226 tion that enlists both of the N-terminal RNA-binding motifs of the protein with separate surfaces of

227 pressed growth plate genes, and enriched for binding motifs of transcription factors with roles in ch

228 rther NOE analysis provided a unique pyrrole binding motif, offering accurate substrate positioning w

229 o-box domain (PBD) of PLK1 interacted with a binding motif on MLL5 (Thr887-Ser888-Thr889), and this i

230 incident interaction with a newly identified binding motif on nucleosome-bound CENP-C.

231 scovery of oncogenic activation of RBMY (RNA-binding motif on Y chromosome), which is absent in norma

232 g strategy that incorporates a serum protein binding motif onto a covalent side-chain staple and appl

233 Furthermore, either the single binding motif or an increase in cytoplasmic bulk through

234 created a mutant of Hsp93 affecting its ClpP-binding motif (PBM) (Hsp93[P-]), which is essential for

235 RAP is mediated by its phosphoinositide (PI)-binding motif (PBM).

236 (-(592)SAV-) and Class II (-(595)CLDM-) PDZ-binding motifs (PBMs).

237 ion Weight Matrix) stacking, for full-length binding motif prediction.

238 cular surface and a conserved "lock and key" binding motifs previously observed to mediate nectin/nec

239 ning octamer-binding protein (NONO), and RNA binding motif protein 14 (RBM14), all reported to be com

240 ell as in cellular mRNAs, is mediated by RNA-binding motif protein 15 (RBM15) and its paralogue RBM15

241 RNA-binding motif protein 20 (RBM20) is essential for normal

242 us missense mutations were identified in RNA-binding motif protein 20 (RBM20), a spliceosome protein

243 several cardiac splice factors, such as RNA-binding motif protein 20 and SF3B1, not only provided im

244 RNA binding motif protein 25 (RBM25) is a putative splicing

245 associates with the core splicing factor RNA binding motif protein 39 (RBM39) and localizes to nuclea

246 sulam promotes the recruitment of RBM39 (RNA binding motif protein 39) to the CUL4-DCAF15 E3 ubiquiti

247 nd instead define it as an extended Class II binding motif PXXPXRpXR, where additional positive charg

248 ted in multiple key residues in the receptor-binding motif (RBM) of RBD and demonstrated their strong

249 protein that regulates FtsZ, and its cognate binding motifs (RBMs) in defining the specific region of

250 lations and measurements, the intramolecular binding motif reduces the apparent affinity of p53 for M

251 nderstanding of binding partners and PAN RNA binding motifs remains incomplete.

252 MshEN domain contains the longest nucleotide-binding motif reported to date.

253 Mutational analysis of the trailer HSPA8 binding motif revealed that this interaction is essentia

254 Several variants of a nucleic acid binding motif (RRM1) of putative transcription factor hn

255 hannel of the 14-3-3 dimer, with both 14-3-3 binding motifs simultaneously participating in protein a

256 atures (e.g. gene sets, transcription factor binding motif sites, etc.).

257 ressed genes often lacking canonical Tcf DNA binding motifs, suggesting a novel mode of direct repres

258 ormation-based analysis of the two homologs' binding motifs suggests a role for dynamic coupling in P

259 Transcriptional co-activator with PDZ-binding motif (TAZ) and Yes-associated protein (YAP) are

260 tion of transcriptional coactivator with PDZ binding motif (TAZ) and Yes-associated protein (YAP) pro

261 AP) and transcriptional coactivator with PDZ-binding motif (TAZ) are related mechanosensory proteins

262 induces transcriptional coactivator with PDZ-binding motif (TAZ) expression, which is required for os

263 AP) and transcriptional coactivator with PDZ-binding motif (TAZ) in mediating mechanotransduction and

264 P) and transcriptional co-activator with PDZ-binding motif (TAZ), are required for the generation of

265 P1) and transcriptional coactivator with PDZ-binding motif (TAZ).

266 Mutation of the tankyrase-binding motif (TBM) on TRF1 (13R/18G to AA) disrupts its

267 the recently proposed tetracysteine-arsenic-binding-motif technology to detect and quantitatively ch

268 AMP with its main chain atoms, a nucleotide-binding motif that appears unique to eukaryotic ADPGKs.

269 REM-CA is an unconventional lipid-binding motif that confers nanodomain organization.

270 MdmX contains an intramolecular binding motif that mimics the binding of the p53 tumor s

271 ys enabled identification of a SigG promoter-binding motif that was supported in vivo by reporter stu

272 within the TE, we identified a module of TF-binding motifs that cooperatively enhanced gene expressi

273 r ALYREF binding sites and identified ALYREF-binding motifs that promote nuclear export of intronless

274 We functionalize these polymers with RNA-binding motifs that sequester polyadenine-containing nuc

275 These include the CP-binding motif, the relative placement of PS stem-loops,

276 d was developed to identify disease-specific binding motifs through integration of bacterial display

277 e RNAs (sgRNAs) integrated with up to 16 MS2 binding motifs to enable robust fluorescent signal ampli

278 ated S-arylation that exploits natural metal-binding motifs to ensure high site selectivity for a pro

279 ctionalities, as the possibility to identify binding motifs, to cluster aptamer families or to compar

280 ect the diversity of both binding motifs and binding motif transitions and the facilitation of their

281 e DNA segments are typified by consensus p63 binding motifs under purifying selection and are associa

282 ively, and are indicative of a change in the binding motif upon replacement of the ligand (GDP versus

283 We also identified WIG1-binding motifs using photoactivatable ribonucleoside-enh

284 A possible 14-3-3 binding motif was identified in one of the two AP2 domai

285 ma' variant lacking the gammaC alphaIIbbeta3-binding motif was more reactive with alphaIIbbeta3 than

286 , we found that the DAT carboxy-terminal PDZ-binding motif was required for DAT recycling and exit fr

287 In addition to known RNA-binding motifs, we detected several protein domains prev

288 isclosed TAFIa inhibitors having a urea zinc-binding motif were used as the starting point for the de

289 ely or independently, and AP1, ETS, and RUNX binding motifs were enriched in the accessible chromatin

290 tion determinants, including a predicted PDZ binding motif, which are critical for its normal membran

291 ural analysis allow us to propose a novel UQ-binding motif, which is completely different compared wi

292 l3 carries both iron-sulfur cluster and zinc-binding motifs, which mediate interactions with Pol31, a

293 ciated peaks are enriched for Zic1 consensus binding motifs, while Zic1-bound peaks are also enriched

294 integrates a database of more than 65 000 TF binding motifs with tools to easily and efficiently scan

295 A site-specific Cu(2+) binding motif within a DNA duplex for distance measureme

296 Here we identify an ATP-binding motif within the NADPH oxidase isoform, NOX4, an

297 We also mutated the major calcium-binding motifs within the T3R domain of full-length Thbs

298 protein/Transcriptional coactivator with PDZ-binding motif, YAP/TAZ) and late (alpha-smooth muscle ac

299 VDR-BVs are enriched in consensus RXR::VDR binding motifs, yet most fell outside of these motifs, i

300 we employed peptide arrays based on zDHHC AR-binding motif (zDABM) sequences of synaptosomal-associat