ライフサイエンスコーパス: binding protein

1 transcriptional coactivator CBP and TATA-box binding protein.

2 ing the two major conformational states of a binding protein.

3 EBNA1, a viral encoded sequence-specific DNA binding protein.

4 ear factor Y subunit C10 (NF-YC10) as a GAPC-binding protein.

5 ic approach identified PfHsp70-1 as a PI(3)P-binding protein.

6 m a polypeptide to a ubiquitous nucleic acid-binding protein.

7 homologue-1 (FXR1) is a muscle-enriched RNA-binding protein.

8 discovered that cohesin SA1 and SA2 are DNA binding proteins.

9 in belonging to the group of EF-hand calcium-binding proteins.

10 s (RNPs), complexes containing mRNAs and RNA binding proteins.

11 es are developed to insert operators for DNA-binding proteins.

12 assette exons enriched in genes encoding RNA binding proteins.

13 l architecture not seen among other retinoid-binding proteins.

14 ractions between regulatory elements and DNA-binding proteins.

15 cellular proteins, particularly nucleic-acid-binding proteins.

16 PEP activity, composed of genes encoding RNA-binding proteins.

17 and the interaction between actin and actin-binding proteins.

18 eins and multiple previously uncharacterized binding proteins.

19 mine the binding selectivities of several HS-binding proteins.

20 the opposing functions of BRCA1 and the p53-binding protein 1 (53BP1)-associated complex in DNA rese

21 for the scaffolding protein Grb2-associated binding protein 1 (Gab1).

22 in stress marker insulin-like growth factor-binding protein 1 (IGFBP-1), were observed with 12-D(3)N

23 Jun activation domain-binding protein 1 (JAB1) is overexpressed in many cancer

24 Poly rC binding protein 1 (PCBP1) is a multifunctional protein t

25 We identify RAS-responsive element binding protein 1 (RREB1), a RAS transcriptional effecto

26 rozygous missense mutations in single-strand binding protein 1 (SSBP1) in 5 unrelated families, leadi

27 nuclear-encoded mitochondrial single-strand binding protein 1 (SSBP1) in patients with apparently do

28 ires the ATR activator, topoisomerase IIbeta-binding protein 1 (TopBP1).

29 vir in this disease.IMPORTANCE Spliced X-box binding protein 1 (XBP-1s), part of the unfolded protein

30 e show that liver-specific ablation of X-box binding protein 1 (XBP1) disrupts the hepatic 12-hour cl

31 ing enzyme 1 (IRE1), which splices the X-box binding protein 1 (Xbp1) mRNA, thereby enabling expressi

32 a manner dependent on Spliced Form of X-box Binding Protein 1 (XBP1s).

33 The multifunctional protein Y-box binding protein 1 (YBX1), is a critical regulator of tra

34 Z-DNA-binding protein 1 (ZBP1; also known as DAI or DLM-1) is

35 target of Myb protein 1 (Stm1; SERPINE1 mRNA-binding protein 1 [SERBP1] in mammals), and recently, la

36 ease, which initiates mRNA splicing of X-box binding protein-1 (XBP1).

37 damaging missense variants in the WW domain binding protein 11 (WBP11) gene in seven unrelated famil

38 (RyR1) interaction with calmodulin and FK506 binding protein 12.6.

39 Insulin-like growth factor (IGF) binding protein 2 (IGFBP2) was discovered and identified

40 Mutations in X-linked methyl-CpG-binding protein 2 (MECP2) cause Rett syndrome (RTT).

41 MECP2 and its product, Methyl-CpG binding protein 2 (MeCP2), are mostly known for their as

42 or peptidoglycan crosslinking by penicillin-binding protein 2 (PBP2) are unable to initiate polarize

43 ith an atypical chemokine receptor chemokine-binding protein 2 variant V41A (ACKR2-V41A; rs2228467).

44 to collagens, such as Ltbp2 (latent TGF-beta-binding protein 2) and Sulf1 (sulfatase 1), which are tr

45 that the XPE gene product DDB2 (damaged DNA binding protein 2), a nucleotide excision repair protein

46 single amino acid replacements in penicillin-binding protein 2X (PBP2X), a major target of beta-lacta

47 ly been challenged by studies of nuclear cap-binding protein 3 (NCBP3).

48 ent peptidoglycan crosslinking by penicillin-binding protein 3 (PBP3/FtsI) initiate polarized divisio

49 eramide-induced RIP of cAMP response element-binding protein 3-like 1 (CREB3L1) also involves RAT.

50 ON-switch system in which the human retinol binding protein 4 (hRBP4) of the lipocalin family intera

51 a(2) -Microglobulin (beta(2) -m) and retinol-binding protein 4 (RBP4) are normally reabsorbed with 'v

52 rotein (GFP), siderocalin (Scn), and retinol-binding protein 4 (RBP4) as model proteins and screened

53 preferentially colocalizes with GATA4 (GATA binding protein 4), a lineage-determining cardiac transc

54 ns of pathogenic deposits containing TAR DNA-binding protein 43 (TDP-43) are evident in the brain and

55 Another protein, TAR DNA binding protein 43 (TDP-43) has been identified in up to

56 TAR DNA-binding protein 43 (TDP-43) has emerged as a key player

57 TDP-43 (TAR DNA-binding protein 43) and FUS (fused in sarcoma) are aggre

58 horylation of intrinsically disordered eIF4E binding proteins (4E-BPs) regulates cap-dependent transl

59 oproteinase-2 and insulin-like growth factor-binding protein 7 was measured at H0, H6, H12, and H24.

60 lloproteinase-2 x insulin-like growth factor-binding protein 7 was poor with respectively an area und

61 ollagen], IGFBP7 [insulin-like growth factor-binding protein-7], and GAL-3 [galectin-3]) were assesse

62 ges in the mitochondrial single-stranded DNA-binding protein, a crucial protein involved in mtDNA rep

63 Ethylene-responsive element binding protein, a member of the APETALA2/ethylene respo

64 The S100 calcium-binding proteins A8 (S100A8) and A9 (S100A9) emerged amo

65 oyltransferase 1a, sterol regulatory element-binding protein, acetyl coenzyme A carboxylase, and fatt

66 Furthermore, we show that a related actin-binding protein, advillin which shares 75% homology with

67 vity for the Drosophila Argonaute family RNA-binding protein AGO1, a component of the miRNA-dependent

68 We observed that C/EBP-alpha (CCAAT/enhancer-binding protein-alpha) can act as a transcription factor

69 d NS for extracellular newly identified RAGE binding protein and between CS and NS for MPO.

70 iple pools is delivered to Sac1 by oxysterol-binding protein and related proteins in exchange for oth

71 g partners non-POU domain containing octamer-binding protein and splicing factor proline/glutamine-ri

72 (MLOs), which majorly consist of RNA and RNA-binding proteins and are formed via liquid-liquid phase

73 ition for binding sites among protective RNA-binding proteins and decay factors, PTBP1 promotes displ

74 Consequently, RNA-binding proteins and mRNA-encoded sequence elements serv

75 ntal stages of other markers such as calcium binding proteins and neuropeptides, helped the identific

76 linkers in regulating multidomain chromatin binding proteins and point to divergent evolution of the

77 ells are reduced but the expression of lipid-binding proteins and transporters is increased(8).

78 n differential recruitment of diacylglycerol binding proteins and, thus, differing downstream phospho

79 t the promoter, recruits the C/EBPbeta (CREB-binding protein) and CBP transcription factors and activ

80 excitement around ProQ as a novel global RNA-binding protein, and its potential to serve as a matchma

81 tent with adipogenesis, and the phospholipid-binding protein annexin A3 (AnxA3), a negative regulator

82 rands and crosslink them: class A penicillin-binding proteins (aPBPs) and complexes of SEDS proteins

83 role of the bifunctional class A penicillin-binding proteins (aPBPs) as well as the L,D-transpeptida

84 nally stabilized by interacting with the RNA-binding protein ApELAV.

85 n's interactions with myosin and other actin-binding proteins are essential for cellular viability in

86 Chlamydomonas reinhardtii, the LHCSR pigment-binding proteins are essential for NPQ.

87 degraded by the proteasome, we uncovered RNA-binding proteins as high-confidence substrates that are

88 ur approach should be adaptable to other DNA-binding proteins as well as small proteins fused to DNA-

89 could validate RBMS1, a barely described RNA-binding protein, as a new target gene for oncogenic miR-

90 s demonstrate that YaaA is a new type of DNA-binding protein associated with the oxidative stress res

91 ruited in phase-separated forms of human RNA-binding proteins associated with SG formation.

92 ogin (SCGN) is a recently discovered calcium-binding protein belonging to the group of EF-hand calciu

93 the G allele interacted with CCAAT/enhancer-binding protein beta transcription factor (TF), while th

94 ures global structural features, such as RNA-binding-protein binding sites and reactivity differences

95 he epigenetic modifier cAMP-response element-binding protein-binding protein/p300 and thereby up-regu

96 he endoplasmic reticulum (ER) immunoglobulin binding proteins (BiPs) are molecular chaperones involve

97 on of mitochondrial single-stranded (ss) DNA-binding protein both influences the ways Twinkle loads o

98 Filaments are regulated by actin-binding proteins, but the nucleotide state of actin is a

99 t decapentaplegic (SMAD)7 and CCAAT/enhancer-binding protein (C/EBP)delta, the transcriptional inhibi

100 cterized one of the newly-discovered heparin-binding proteins, C-type lectin 14a (CLEC14A), a member

101 irm that the nine stripes ascribed to myosin binding protein-C are not related to the titin sequence

102 -terminal domains C0 to C7 of cardiac myosin binding protein-C) fragment and an insoluble C'-terminal

103 -terminal domains C0 to C7 of cardiac myosin binding protein-C)-sc returned pCa(50) and k(tr) to cont

104 ned to the filament domain containing myosin binding protein-C, the "C-zone." Myosin motors in domain

105 ase factor homolog C12orf65 (mtRF-R) and RNA binding protein C6orf203 (MTRES1) eject the nascent chai

106 This sequence-specific DNA-binding protein can disrupt EBV latency by driving the t

107 s, although both DNA-binding and microtubule-binding proteins can diffuse on the negatively charged b

108 ablish that non-amyloid self-assembly of RNA-binding proteins can drive a form of epigenetics beyond

109 at RsmA associates with and that the two RNA-binding proteins can exert regulatory effects on common

110 On the protein side, only DNA-binding proteins can perform rotation-coupled diffusion

111 of the protein acetyltransferases p300/CREB-binding protein (CBP).

112 PK to selectively induce EP300, but not CREB-binding protein (CBP).

113 Cap-binding protein (CBP)20 and its binding partner CBP80 ha

114 classical NLSs within the cold-inducible RNA-binding protein (CIRBP).

115 (Golgi-localized, gamma-ear-containing, ARF-binding protein), clathrin adaptors, and clathrin.

116 etic perturbation that cellular nucleic acid-binding protein (CNBP) and La-related protein 1 (LARP1),

117 s of FliY, where the l- enantiomer-substrate-binding protein complex interacted more efficiently with

118 growing body of evidence indicates that RNA binding proteins control an array of processes in beta-c

119 lysaccharide monooxygenase (LPMO) and copper binding protein CopC share a similar mononuclear copper

120 ded on activation of cAMP-responsive element-binding protein (CREB) for induction of Ralpha2 expressi

121 e transcription factor cAMP response element-binding protein (CREB) to enhance the expression of prot

122 found that loss of the cAMP response element-binding protein (CREB) transcription factor significantl

123 N, a plant homologue of mammalian C-TERMINAL BINDING PROTEIN (CtBP), antagonistically regulates plant

124 our results showed increased binding of RNA-binding protein CUGBP1 with occludin and E-cadherin gene

125 Aggregates of a prion-like RNA-binding protein, cytoplasmic polyadenylation element-bin

126 xidative stress regulator (bosR) and decorin binding protein (dbpBA) by utilizing bioluminescent B. b

127 Single-strand DNA binding protein did not affect PcrA translocation veloci

128 The RNA polymerase-binding protein DksA, together with the alarmone nucleot

129 erminants promoting glycan binding to glycan-binding proteins due to the ambiguity in microarray fluo

130 d by recruitment of the microtubule plus end-binding protein EB1/EBP-2 around the wound and actin rin

131 Here, we found that the noncanonical 5' cap-binding protein eIF3d was activated in response to metab

132 function, is controlled by mTORC1 and EIF-4E Binding Proteins (EIF4EBPs).

133 f a newly synthesized mRNA by a class of RNA binding proteins (ELAVs).

134 ontrast, the lower net charge on microtubule-binding proteins enables them to diffuse more quickly th

135 CRISPR knockout of LIN28B-an oncofetal RNA-binding protein exerting diverse effects via negative re

136 studies demonstrate that adipose fatty acid binding protein (FABP4) promotes obesity-associated brea

137 Fatty acid binding proteins (FABPs) serve as intracellular chaperon

138 arrangements, disorder within the chromatin-binding proteins facilitates promiscuous binding to a wi

139 eripheral membrane protein of the fatty acid-binding protein family that functions in the formation a

140 CID tools such as the FK506-binding protein-FKBP-rapamycin-binding- (FKBP-FRB)-rapam

141 ach immunophilin family, cyclophilins, FK506 binding proteins (FKBPs), and parvulins in bacteria.

142 This motif binds the RNA binding protein FMR1 and directs miRNA loading into exos

143 des a way to expand the repertoire of glycan-binding proteins for further study.

144 related protein 6 (Larp6) is a conserved RNA-binding protein found across eukaryotes that has been su

145 ed that Fabp5, an abundant cytoplasmic lipid-binding protein found in brain endothelial cells, makes

146 SERBP1 is the first example of an RNA-binding protein functioning as a central regulator of ca

147 Mutations in the RNA-binding protein FUS cause amyotrophic lateral sclerosis

148 Dysregulation of the DNA/RNA-binding protein FUS causes certain subtypes of ALS/FTD b

149 The RNA-binding protein fused in sarcoma (FUS) forms physiologic

150 show that the phosphorylation of the RNA-DNA binding protein fused in sarcoma (FUS) is higher in Itga

151 to the dynamic process of guanine nucleotide-binding protein (G-protein) activation.

152 LGALS2 encodes the glycan-binding protein Galectin 2 (Gal2), which is predominantl

153 , which upregulates genes encoding guanylate-binding proteins (GBPs) and inducible nitric oxide synth

154 l processes through interactions with glycan-binding proteins (GBPs).

155 We discover an expansion of odorant-binding-protein genes, some expressed specifically in br

156 and is dependent on expression of the AMPAR-binding protein GRIP1.

157 Galectin-1 (Gal1), an endogenous glycan-binding protein, has emerged as a regulator of immune ce

158 pathologically associated with tau (e.g. RNA binding protein HNRNPA1).

159 We additionally show that the related RNA-binding proteins hnRNPF and hnRNPH bind directly to tRF-

160 lls revealing upregulation of CCAAT/enhancer-binding protein homologous protein and immunoglobulin he

161 Here, we report that the RNA-binding protein HuR (ELAVL1) forms complexes with NAFLD-

162 g p53 protein synthesis by degrading the RNA-binding protein HuR in response to UV radiation.

163 ized livers through its interaction with RNA-binding protein HuR.

164 ere, we report the identification of the RNA-binding protein HuR/ELAVL1 as a central oncogenic driver

165 In this study, we used TRIBE (targets of RNA-binding proteins identified by editing) as an approach t

166 Together, our work revealed VEZF1 as a G4-binding protein, identified a novel regulatory mechanism

167 in-like growth factor (IGF)-1 as well as IGF-binding protein (IGFBP)-3.

168 ort and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)" route in allergic asthma and

169 and were the major cellular source of IL-22 binding protein (IL-22BP) at steady state.

170 arcoma (FUS) is a ubiquitously expressed RNA-binding protein implicated in familial ALS and frontotem

171 volution of chlorosis, describe a biliverdin-binding protein in vertebrates, and introduce a function

172 on of free PI(4)P via expression of a PI(4)P-binding protein in yeast strongly inhibited TBSV replica

173 e roles of the plant complement of small GTP-binding proteins in these cellular processes are describ

174 g, a function for afadin and adducin-1 actin binding proteins in thrombin-induced endothelial barrier

175 iciently and selectively captured known CS-E-binding proteins in vitro and in cells.

176 , and that they bound a diverse array of RNA binding proteins, including p300 but not CBP.

177 Many DNA-binding proteins induce changes in the structure of the

178 ptor channel, ryanodine receptor, and Ca(2+)-binding proteins inside of the ER lumen.

179 or receptor A (PDGFRA), as well as novel RNA-binding protein interactors ZC3H14 (zinc finger CCCH-typ

180 Septins are GTP-binding proteins involved in diverse cellular processes

181 on protein A (RPA), a major eukaryotic ssDNA-binding protein, is essential for all metabolic processe

182 rk of actin filaments and associated F-actin-binding proteins, is fundamentally important in eukaryot

183 organic matter, such as hydrophobic surface binding proteins, laccases (AA1_1), xylanases (GH10, GH1

184 ta support a role for the predicted c-di-GMP-binding protein LapD in inhibiting LapG-dependent disper

185 , Procalcitonin (PCT) and Lipopolysaccharide-binding protein (LBP).

186 with a peripheral membrane-associated Ca(2+)-binding protein, likely ANXA1.

187 Targeting the actin-binding proteins LIMK1 and LIMK2 significantly diminishe

188 a, and of HBL-1 for lin-29b, whereas the RNA-binding protein LIN-28 coordinates LIN-29 isoform activi

189 teomic analyses, we demonstrate that the RNA-binding protein LIN28B, which is developmentally express

190 (HSPCs) caused by high expression of the RNA-binding protein Lin28b.

191 vel its details, we identified all phosphate-binding protein lineages in the Evolutionary Classificat

192 macrophages, within the CSF express the iron-binding protein lipocalin-2 (LCN2) and its receptor SCL2

193 n proteins, we uncover a role for the dynein-binding protein LIS1 in promoting the formation of activ

194 sfer (smFRET) measurements of the amino acid binding protein LIV-BPSS at sub-millisecond resolution.

195 In retinal-binding proteins, mainly two mechanisms exist to store t

196 s requiring the involvement of several actin-binding proteins, many of which are still unidentified.

197 ave shown that 5-HT(3A)-ICD fused to maltose-binding protein (MBP) directly interacts with RIC-3, wit

198 c degenerate' DNA motif and fused to Maltose Binding Protein (MBP).

199 at three maternally deposited Drosophila RNA-binding proteins (ME31B, Trailer Hitch [TRAL], and Cup)

200 From this screen, we identified an RNA binding protein, Musashi (msi), as one of the possible g

201 Evolutionarily conserved RNA-binding protein Musashi1 (Msi1) can regulate development

202 A novel cap-binding protein, NCBP3, was recently proposed to form an

203 Insoluble, hyperubiquitylated TAR DNA-binding protein of 43 kDa (TDP-43) in the central nervou

204 sociated with loss of eIF4E, the mRNA 5' cap-binding protein of the initiation complex and binding pa

205 sociated with loss of eIF4E, the mRNA 5'-cap binding protein of the initiation complex and binding pa

206 nables them to diffuse more quickly than DNA-binding proteins on both biopolymers.

207 ent formation and may antagonize other ssDNA-binding proteins on RPA-coated ssDNA.

208 Blocking PKR using PKR-K296R, the TAR RNA binding protein or PKR-KO cells, reduces RAN protein lev

209 Galectins are carbohydrate-binding proteins overexpressed in bladder cancer (BCa) c

210 density of structures expressing the calcium-binding proteins parvalbumin, calbindin, and calretinin.

211 aluated pbp expression, levels of penicillin-binding protein (PBP) 5 (PBP5) and beta-lactam binding a

212 to bind to the allosteric site of penicillin-binding protein (PBP)2a, resulting in opening of the act

213 adsorption system featuring immobilized P(i)-binding proteins (PBP) has recently attracted attention

214 single amino acid substitution in penicillin-binding protein PBP2X that conferred a 2-fold increased

215 actam pyrazolidinone that targets penicillin-binding proteins (PBPs) and incorporates a siderophore m

216 Penicillin binding proteins (PBPs) catalyzing transpeptidation reac

217 n antibody specific to G4-DNA and the G4-DNA-binding protein PC4 bind to the Atg7 PQFS.

218 ure of the DNA-binding domain of a model ASO-binding protein PC4, in complex with a full PS 2'-OMe DN

219 for calcium management (calmodulin, calcium-binding proteins), pH regulation (V-type proton ATPase),

220 Consequently, RNA-binding proteins play a critical role in the regulation

221 to C1q suggest an overlooked role as a lipid-binding protein, possibly generalizable to other C1q/TNF

222 To identify RNA binding proteins potentially driving these patterns, we

223 tin monomers directly, formins use the actin-binding protein profilin to dynamically load actin monom

224 s to functional neurons by depleting the RNA-binding protein PTB (also known as PTBP1).

225 s through experimental examples with the RNA-binding protein Puf4.

226 A Ran binding protein (RanBP) homolog, CpRbp1, from Cryphonect

227 DNA binding proteins rapidly locate their specific DNA targe

228 om our lab implicate autoimmunity to the RNA binding protein (RBP) heterogeneous nuclear ribonucleopr

229 strained, and enriched for cis-eQTLs and RNA-binding protein (RBP) interactions.

230 ed that La-related protein 4 (LARP4), an RNA-binding protein (RBP) known to enhance mRNA stability, w

231 hly specific recognition of ribose by ribose-binding protein (RBP) to develop a single-protein ribose

232 ritin, soluble transferrin receptor, retinol-binding protein (RBP), 25-hydroxy vitamin D, folate, and

233 (dCas9)-based CARRY (CRISPR-assisted RNA-RNA-binding protein [RBP] yeast) two-hybrid assay to assess

234 ighly interconnected network enriched in RNA-binding proteins (RBPs) and EV cargoes.

235 RNA binding proteins (RBPs) are a large protein family that

236 RNA-binding proteins (RBPs) comprise a large class of over 2

237 RNA binding proteins (RBPs) frequently regulate the expressi

238 The cell-context dependency for RNA binding proteins (RBPs) mediated control of stem cell fa

239 ated mRNA decay and associate with major RNA-binding proteins (RBPs) such as Hfq and ProQ.

240 ndividual guide RNAs (gRNA), we identify RNA-binding proteins (RBPs) that influence the formation of

241 mental stress are frequently mediated by RNA-binding proteins (RBPs).

242 nts demonstrated that cAMP response elements binding protein regulates the expression of PGC1alpha in

243 MEIOB, a meiosis-specific ssDNA-binding protein, regulates early meiotic recombination.

244 Finally, we observed a DNV burden in RNA-binding-protein regulatory sites (OR = 1.13, 95% CI 1.1-

245 OSBPL1 encodes the full-length oxysterol-binding protein-related protein ORP1L, which transports

246 lical protein; and LUX ARRYTHMO (LUX), a DNA-binding protein required to recruit the evening complex

247 c condensate that consists of ubiquitous RNA-binding proteins, revealing an unanticipated mechanism f

248 f TRAMP components with multiple nuclear RNA binding proteins, revealing preferential colocalization

249 s and are enriched with binding sites of RNA-binding proteins, RNA structure-changing variants and tr

250 -binding activity of the single-stranded DNA-binding protein RPA, efficient DNA replication through e

251 the protective capacity of the single-strand-binding protein RPA.

252 ransport of cargo by motor proteins, many MT-binding proteins seem to adopt diffusional motility as a

253 We identify the RNA-binding protein SERBP1 as a novel regulator of glioblast

254 in other proteins, suggesting that sulfatide-binding proteins share common binding mechanisms.

255 ptor interacting protein 1 (GRIP1), an AMPAR-binding protein shown to regulate the trafficking and sy

256 eosomes can influence, or be altered by, DNA-binding proteins, single-molecule techniques are increas

257 s is maintained by sterol regulatory element-binding proteins (SREBPs), membrane-bound transcription

258 LMO2 and LDB1 as well as single-stranded DNA-binding protein (SSBP) cofactors and DNA-binding basic h

259 ribosome complexes are associated with mRNA-binding proteins, stress granule, and P-body proteins, w

260 al for using genetically encoded periplasmic binding proteins such as RBP to measure metabolites in d

261 RG/RGG and RSY regions in numerous other RNA-binding proteins suggests that the interaction of TNPO1

262 eriod, the general transcription factor TATA binding protein (TBP) is replaced by its paralogue, TBPL

263 cent subunit Spt8 interact with the TATA box-binding protein (TBP)(2,7,15-17).

264 yglutamine (polyQ) expansion in the TATA box-binding protein (TBP).

265 The RNA binding protein TDP-43 forms intranuclear or cytoplasmic

266 Mutations in TARDBP, encoding the RNA-binding protein TDP-43, are one cause of ALS, and TDP-43

267 pressing ALS-linked gene mutants for TAR DNA-binding protein (TDP-43) and superoxide dismutase 1 (SOD

268 rexcitability and mislocalization of the RNA-binding protein TDP43 are highly conserved features in a

269 HOAP is a telomere-binding protein that has a conserved role in Drosophila,

270 The FinO-domain-protein ProQ is an RNA-binding protein that has been known to play a role in os

271 Cofilin-2 is an actin-binding protein that is predominantly expressed in skele

272 Here, we demonstrated that GULP1 was a KEAP1-binding protein that maintained actin cytoskeleton archi

273 ngs demonstrate that FUS is an important RNA-binding protein that mediates translational repression t

274 hogen Pseudomonas aeruginosa, RsmA is an RNA-binding protein that plays critical roles in the control

275 Mental Retardation Protein (FMRP) is an RNA binding protein that regulates translation and is requir

276 Pumilio is an RNA-binding protein that represses a network of mRNAs to con

277 e FMR1 gene and loss of encoded FMRP, an RNA binding protein that represses translation of some of it

278 RADX is a mammalian single-stranded DNA-binding protein that stabilizes telomeres and stalled re

279 long 26 hr period phenotype, encodes an RNA-binding protein that stabilizes the ck-1a transcript, re

280 crystallographically characterized porphyrin-binding protein that was programmed to not only bind a s

281 actor binding but also to recruit methyl-CpG binding proteins that affect chromatin structure through

282 ensor and the transporter, utilize galactose-binding proteins that also bind glucose with the same af

283 (fused in sarcoma) are aggregation-prone RNA-binding proteins that in ALS can mislocalize to the cyto

284 Here we have developed monobodies, synthetic binding proteins, that bind the N-terminal four-helix bu

285 Among the partially disordered chromatin-binding proteins, the H1 linker histone influences a myr

286 between adjacent wall peptides by penicillin-binding proteins to confer robustness and flexibility.

287 ents in cells could help to direct accessory binding proteins to different actin cytoskeletal structu

288 they transiently secrete fibronectin and its binding proteins to form bridges of extracellular matrix

289 the protein-, nucleic acid- and small ligand-binding proteins (to study the cross-predictions).

290 teracts with the TRFH domain of the telomere binding protein TRF2.

291 interferon-gamma fragment and the chemokine-binding protein UL22A, respectively.

292 ogous protein and immunoglobulin heavy chain binding protein UPR-response genes.

293 es (VBSs) from different nonhomologous actin-binding proteins use conserved helical motifs to associa

294 evised a cell-based functional screen of RNA-binding proteins using a let-7 sensor luciferase reporte

295 Three IgE-binding proteins were identified: legumin (Pru du 6), al

296 ery of two previously unknown surface glycan binding proteins which facilitate glycosaminoglycan impo

297 tion that both KWL proteins are carbohydrate-binding proteins with distinct and likely tissue-related

298 ating evidence suggests participation of RNA-binding proteins with intrinsically disordered domains (

299 nd that PRC2 interacts with the nucleic acid-binding protein Ybx1.

300 RNA-binding protein ZFP36L1 functions as a tumor suppressor