ライフサイエンスコーパス: -binding protein

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

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

3 pecifically recruited one of the two poly(A)-binding proteins, PABP2, and one of the six cap-binding

4 domain homology model and two acetylcholine-binding protein homologs.

5 at mite group 13 allergens of the fatty acid-binding protein (FABP) family are sensed by an evolution

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

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

8 ed to the human single-stranded nucleic acid-binding protein Pur-alpha, as a component of germ granul

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

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

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

12 sions involves flightless I (FliI), an actin-binding protein that contains a leucine-rich-repeat (LRR

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

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

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

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

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

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

19 (shootin1) and show that, unlike known actin-binding proteins, SHTN1's actin binding activity is intr

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

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

22 s gatekeepers for the binding of other actin-binding proteins.

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

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

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

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

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

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

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

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

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

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

33 in 1beta (nsp1beta) and host protein poly(C)-binding protein (PCBP) 1 or 2 with the viral genome.

34 ng of complement inhibitors factor H and C4b-binding protein.

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

36 Mutations in the calcium-binding protein calsequestrin cause the highly lethal fa

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

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

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

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

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

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

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

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

45 ing Complex (CBC), consisting of Nuclear Cap-Binding Protein 1 (NCBP1) and 2 (NCBP2), associates with

46 or subunit) and HIV-1 genes, and nuclear cap-binding protein 1 (NCBP1)/CBP80 is a component of HIV-1

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

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

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

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

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

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

53 Many chromatin-binding proteins and protein complexes that regulate tra

54 ed by the orchestrated function of chromatin-binding proteins that tightly control the expression of

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

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

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

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

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

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

61 ns that associate with the chromatin and DNA-binding protein Barrier-to-autointegration factor (BAF).

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

63 the protein CHD8 [chromodomain-helicase-DNA-binding protein 8]) are among the most common mutations

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

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

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

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

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

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

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

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

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

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

74 -synuclein in Parkinson disease, and TAR DNA-binding protein 43 in amyotrophic lateral sclerosis.

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

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

77 he nucleus, where it associates with the DNA-binding protein LAG-1/CSL to activate target gene transc

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

79 ractions between regulatory elements and DNA-binding proteins.

80 Transcription factors are DNA-binding proteins that have key roles in gene regulation(

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

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

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

84 experimentally assayed for thousands of DNA-binding proteins.

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

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

87 get DNA by adjacently bound programmable DNA-binding proteins.

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

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

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

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

92 SREBF1 encodes sterol regulatory element-binding protein 1 (SREBP1), which promotes the transcrip

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

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

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

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

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

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

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

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

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

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

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

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

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

106 lloproteinase-2 x insulin-like growth factor-binding protein 7 and of renal resistive index to predic

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

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

109 lloproteinase-2 x insulin-like growth factor-binding protein 7 was unable to differentiate transient

110 alysis identified insulin-like growth factor-binding protein-5 (IGFBP-5) as a downstream target of JP

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

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

113 coli periplasmic glycerol-3-phosphate (G3P)-binding protein UgpB can serve, in the absence of its su

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

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

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

117 Galectin-3 is a glycan-binding protein (GBP) that binds beta-galactoside glycan

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

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

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

121 an evolutionarily conserved family of glycan-binding proteins, have broad influence in tumor progress

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

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

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

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

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

127 Small GTP-binding proteins represent a highly conserved signaling

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

129 al antibodies (mAbs) raised against factor H-binding protein (fHbp) and Neisserial Heparin-Binding An

130 for HA-mediated motility, RHAMM, and the HA-binding protein TNF-stimulated gene 6 protein (TSG6).

131 NRAMP-1), transferrin, lactoferrin, and heme-binding proteins.

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

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

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

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

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

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

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

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

140 r findings demonstrate that GULP1 is a KEAP1-binding protein that regulates KEAP1-NRF2 signaling in U

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

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

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

144 D8, a Synaptotagmin-like Mitochondrial lipid-binding Proteins (SMP) domain-containing ER transmembran

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

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

147 t protein (MCP-1), autotaxin (ATX), and Mac2-binding protein (Mac2BP) were measured over 48 weeks.

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

149 We found that DNA-binding and microtubule-binding proteins can diffuse on each other's substrates;

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

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

152 entified signal-transducing adaptor molecule-binding protein (STAMBP) and ubiquitin-specific protease

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

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

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

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

157 a3 integrin and Galpha13 (guanine nucleotide-binding protein subunit alpha 13), resulting in the cons

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

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

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

161 by Osh1, a member of the conserved oxysterol-binding protein (OSBP) family of lipid transfer proteins

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

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

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

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

166 s of a beta-lactamase, PC1, and a penicillin-binding protein poorly acylated by beta-lactam antibioti

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

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

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

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

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

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

173 s conferred by mosaic variants of penicillin-binding protein 2 (PBP2) that have diminished capacity t

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

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

176 tidase (TP) activity catalyzed by penicillin-binding proteins (PBPs) separate into a pair of concentr

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

178 arget sites such as the ribosome, penicillin-binding proteins, and topoisomerases in a pharmacologica

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

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

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

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

183 ludes conserved pyridoxal 5'-phosphate (PLP)-binding proteins that play a critical role in the homeos

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

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

186 ramatically enhances recognition of PS by PS-binding proteins such as GAS6, PROS, and TIM1.

187 igh-affinity, environmentally hardy receptor-binding proteins.

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

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

190 Retinol-binding protein-4 (RBP4) is elevated in serum and adipos

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

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

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

194 ch was catalysed by RhoA GTPase via the RhoA-binding protein, rhotekin.

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

196 We here show in Drosophila that RIM-binding protein (RIM-BP) connects release sites physical

197 RNA-binding protein ZFP36L1 functions as a tumor suppressor

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

199 mental retardation protein (FMRP) is an RNA-binding protein abundant in the nervous system.

200 cytes expressed Lin28b, which encodes an RNA-binding protein associated with fetal hematopoietic gene

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

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

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

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

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

206 TDP-43 is an RNA-binding protein which forms aggregates in neurons of ALS

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

208 , RNA editing, nuclear pore composition, RNA-binding protein motif enrichment, and RNA secondary stru

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

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

211 w that ZC3H5 is an essential cytoplasmic RNA-binding protein.

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

213 in Arabidopsis that employed a designer RNA-binding protein as a psbA RNA affinity tag.

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

215 suggesting a feedback between effective RNA-binding protein dosage and protein quality control in C9

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

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

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

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

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

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

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

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

224 FUS is a nuclear RNA-binding protein, and its cytoplasmic aggregation is a pa

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

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

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

228 ntify and characterize a conserved SMALL RNA-BINDING PROTEIN 1 (SRBP1) family that mediates non-cell-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

244 RNA-binding proteins (RBPs) are key mediators of RNA metabol

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

246 RNA-binding proteins (RNA-BPs) play critical roles in develo

247 The human genome encodes for over 1,500 RNA-binding proteins (RBPs), which coordinate regulatory eve

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

249 the crosstalk between cell signaling and RNA-binding proteins.

250 Interactions between RNA-binding proteins (RBPs) and RNAs are critical to cell bi

251 the human genome that are recognized by RNA-binding proteins (RBPs), generated as part of the Encycl

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

253 poral gene regulation is often driven by RNA-binding proteins that harbor long intrinsically disorder

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

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

256 taining complexes reproducibly contained RNA-binding proteins that were previously found associated w

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

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

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

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

261 thod's wide applicability in identifying RNA-binding proteins.

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

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

264 c finger (TZF) domains are found in many RNA-binding proteins (RBPs) that regulate the essential proc

265 Here, we uncover a network of RNA-binding proteins (RBPs) that enhances the translation ef

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

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

268 Our analysis of RNA-binding proteins reveals ILF3 as a potential regulator o

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

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

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

272 such as trypanosomes depends heavily on RNA-binding proteins that influence mRNA decay and translati

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

274 of similar mechanisms governed by other RNA-binding proteins.

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

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

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

278 ogenesis is tightly regulated by several RNA-binding proteins, including Lin28A/B, which represses le

279 The sequence-specific RNA-binding proteins PTBP1 (polypyrimidine tract-binding pro

280 agile X protein family consists of three RNA-binding proteins involved in translational regulation.

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

282 Opposing gradients of two RNA-binding proteins Imp and Syp comprise the intrinsic temp

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

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

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

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

287 show that fission yeast Mso1 is also a Sec1-binding protein and Mso1 and Sec1 localize to the divisi

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

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

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

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

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

293 e identification of membrane heparan sulfate-binding proteins is challenging because of their low abu

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

295 our co-crystal structures of lab-evolved TAR-binding proteins (TBPs) in complex with HIV-1 TAR.

296 n replacement of the TFIID complex with TATA-binding protein (TBP), and PRO-seq experiments revealed

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

298 binding proteins PTBP1 (polypyrimidine tract-binding protein 1) and HNRNP L (heterogeneous nuclear ri

299 t expression of the NKG2D ligand ULBP2 (UL16-binding protein 2) is associated with bacterial degradab

300 ) can form heterodimers with small vasohibin-binding protein (SVBP) and were recently shown to regula