ライフサイエンスコーパス: RNA recognition motif

1 nd that it does not have the postulated RRM (RNA recognition motif).

2 ulator of DNA demethylation that contains an RNA recognition motif.

3 and RNPC1b, both of which contain an intact RNA recognition motif.

4 ed protein harboring both a PPR tract and an RNA recognition motif.

5 also phosphorylates RD at sites next to its RNA recognition motif.

6 larger neutral proteins that also include an RNA recognition motif.

7 iple arginine-serine (RS) repeats but had no RNA recognition motif.

8 ng an activation domain, an RS domain and an RNA recognition motif.

9 arginine/serine-rich domains separated by an RNA recognition motif.

10 the SR family of splicing factors, lacks an RNA recognition motif.

11 FLS2 and EFR transcripts in vivo through its RNA recognition motif.

12 itional domains present as insertions in the RNA-recognition motif.

13 des a nuclear-localized protein featuring an RNA-recognition motif.

14 that differs from those observed with other RNA recognition motifs.

15 two protein subdomains, each containing two RNA recognition motifs.

16 ated splicing factors that possess identical RNA recognition motifs.

17 al abnormal visual protein and contain three RNA recognition motifs.

18 and GRY-RBP) in that it does not contain any RNA recognition motifs.

19 epitope located in the first of HuR's three RNA recognition motifs.

20 kDa protein that contains three nonidentical RNA recognition motifs.

21 -269 TDP-43 fragment, which comprise the two RNA recognition motifs.

22 We found that RNA recognition motif 1 (RRM1) in SRSF1 binds PP1 and re

23 ructural changes suggest that the N-terminal RNA recognition motif 1 (RRM1) is more promiscuous for c

24 then deleted of other motifs indicated that RNA recognition motif 1 (RRM1) is required for nuclear e

25 d single-chain (scFv) antibodies against the RNA recognition motif 1 (RRM1) of TDP-43, which is invol

26 We mapped the leRNA binding function to RNA recognition motif 1 of La and showed that while wild

27 protein (PAB1) in which removal of the RRM1 (RNA recognition motif 1) domain of PAB1 blocked both the

28 and a nuclear retention element (NRE) in the RNA recognition motif 2 (RRM2) domain.

29 Set1 lacking RNA recognition motif 2 (RRM2) showed reduced in vivo cr

30 overlaps with the RNA-binding site involving RNA recognition motif 2 (RRM2).

31 erexpression of HuR deletion mutants lacking RNA recognition motif 3 (RRM 3) does not exert a stabili

32 r the conserved C-terminal domain of U2AF59 (RNA recognition motif 3), which has been implicated in p

33 nventional motif, (296)EEAMAIAS(304), in the RNA recognition motif 3.

34 Ser-513 phosphorylation within the RNA recognition motif 4 enhanced heterogeneous ribonucle

35 PRPAAAAAA500, separating the four N-terminal RNA recognition motifs (80%) from the C-terminal homodim

36 Mutation of an arginine in the RNA recognition motif abrogated in vivo binding and the

37 In addition to a conserved RNA recognition motif and a C-terminal RNA binding domai

38 C-terminal domain that contains an atypical RNA recognition motif and a short basic motif (SBM) adja

39 factors characterized by the presence of an RNA recognition motif and an arginine/serine domain, are

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

41 nding protein 3 and D11Bwg0517e) contains an RNA recognition motif and is classified as a member of t

42 series of chimeric proteins by swapping the RNA recognition motif and RS domains between SRrp86 and

43 beta-karyopherin fold of Tnpo3 embraces the RNA recognition motif and RS domains of the cargo.

44 a protein containing a single amino-terminal RNA recognition motif and two carboxy-terminal domains r

45 of the SR protein superfamily containing one RNA recognition motif and two serine-arginine (SR)-rich

46 perfamily of splicing factors containing one RNA recognition motif and two serine-arginine (SR)-rich

47 An RNA recognition motif and Walker motif in the metazoan-s

48 of proteins defined by three amino-terminal RNA recognition motifs and a carboxyl-terminal SPOC (Spe

49 ncodes nuclear 600 kDa proteins that contain RNA recognition motifs and a conserved C-terminal sequen

50 es, including a RNA-binding protein with two RNA recognition motifs and a zinc knuckle (ZD7), and a D

51 scriptional activation/repression domain and RNA recognition motifs and has a significant role in the

52 Proteins containing RNA recognition motifs and involved in splicing, messeng

53 an RNA splicing modulator that contains two RNA recognition motifs and multiple hexapeptide repeats.

54 tructure unexpectedly composed of a modified RNA-recognition motif and two additional domains present

55 SR proteins consist of one or two RNA-recognition motifs and a characteristic arginine/ser

56 in encoded by PpTEL1 contains two N-terminus RNA-recognition motifs, and a third C-terminus non-canon

57 Although the RNA recognition motif appears to reside solely in alpha-

58 P1 and PCBP2) are RNA-binding proteins whose RNA recognition motifs are composed of three K homology

59 eletion mutants, sequences C-terminal to the RNA recognition motifs are shown to contribute to the fo

60 MAN1, through the RNA recognition motif, associates with R-Smads but not S

61 set1, which encodes a protein containing an RNA recognition motif at its amino terminus and a SET do

62 its high affinity bZLM and mutations in the RNA recognition motif at suggested RNA binding sites pri

63 ponse element is composed of two consecutive RNA recognition motifs at the amino terminus of vertebra

64 Both proteins use their RNA-recognition motifs but not the Zinc-finger region fo

65 forms lack the arginine/serine-rich (RS) and RNA recognition motifs characteristic of PGC-1alpha1.

66 NP) mRNA as bait, we identified the cellular RNA-recognition motif containing RNA-binding protein G-r

67 complex containing RNA Binding Region (RNP1, RNA recognition motif) Containing 3 (RNPC3) that is foun

68 teracting protein (RIP) family and Organelle RNA Recognition Motif-containing (ORRM) family are essen

69 s studies have concentrated on the canonical RNA recognition motif-containing poly(A) binding protein

70 rent mechanism than previously characterized RNA recognition motif-containing poly(A) binding protein

71 ng protein (RIP) family and ORRM1 (Organelle RNA Recognition Motif-containing protein 1) have been re

72 (ASI1), a bromo-adjacent homology domain and RNA recognition motif-containing protein, from a forward

73 PSF and p54(nrb) are RNA recognition motif-containing proteins with well-esta

74 et structure, which appears similar to other RNA recognition motif-containing proteins.

75 f hnRNPA1 is sufficient to mediate LLPS, the RNA recognition motifs contribute to LLPS in the presenc

76 PD2 is a modular protein composed of RNA recognition motif, DEAD-boxes, an aspartic/serine (D

77 biological substrate when a carboxy-terminal RNA recognition motif domain binds tightly and specifica

78 The RNA recognition motif domain of MINT (which binds the OC

79 o the spectrin domain of eIF3a occurs in its RNA recognition motif domain where eIF3j also binds in a

80 The tandem RNA recognition motif domains (RRM1,2) of U2AF65 adopt c

81 Two RNA recognition motif domains and a C-terminal binuclear

82 leolin is required for binding, and the four RNA recognition motif domains are included in the isofor

83 allel coiled-coil that positions two of four RNA recognition motif domains in an unprecedented arrang

84 -amino-acid-long protein that contains three RNA recognition motif domains in tandem and a distinct C

85 proteins, we propose a model where the four RNA recognition motif domains in the heteromeric PSF.p54

86 U2AF homology motifs (UHMs) are atypical RNA recognition motif domains that mediate critical prot

87 , share extensive homology, including tandem RNA recognition motif domains.

88 etween the second and third of the three HuR RNA recognition motif domains.

89 RRM, or RNA-recognition motif, domains are the largest class of

90 ions or posttranslational acetylation in its RNA recognition motifs) drove TDP-43 demixing into intra

91 es, RNA-binding motif protein-15 (RBM15), an RNA recognition motif-encoding gene with homology to Dro

92 splicing effector protein composed of a core RNA recognition motif flanked by two arginine-serine-ric

93 s resembling the family of ribonucleoprotein/RNA-recognition motif fold proteins establishes a struct

94 The minimal RNA recognition motif for TGT has been found to involve

95 e cDNA, designated Pa-RRM-GRP1 (Prunus avium RNA recognition motif glycine-rich protein 1), contains

96 The RBP nucleolin, with four RNA-recognition motifs, has been implicated in cell prol

97 the open conformation of U2AF2 with an inter-RNA recognition motif hydrogen bond, in agreement with a

98 Notably, however, a tryptophan in the pseudo-RNA recognition motif implicated in a key contact with t

99 Finally, we showed that the RNA recognition motif in Rbm24 is required for binding t

100 Two N-terminal RNA recognition motifs in ASF/SF2 control access to the

101 The predicted FPA protein contains three RNA recognition motifs in the N-terminal region.

102 re are at least 213 human proteins harboring RNA recognition motifs, including FUS and TDP-43, raisin

103 yeIF4B contributes to these activities, the RNA recognition motif is dispensable.

104 ation and repression domains (and not the RS/RNA recognition motif) is what determines the gene progr

105 Located in the RNA recognition motif, K315/K316 acetylation reduced RNA

106 karyotic PAPs, and lacks a recognizable RRM (RNA recognition motif)-like domain.

107 UTRs mRNAs through a previously unidentified RNA recognition motif-like motif.

108 nd was not observed with PTB mutants lacking RNA recognition motifs located in the C-terminal third o

109 ting that stable RNA binding mediated by the RNA-recognition motifs may be required for shuttling.

110 d1-polymerase II binding defect, and an Nab3-RNA recognition motif mutation.

111 binds both mRNA and rRNA fragments due to an RNA recognition motif near its C terminus.

112 eIF3-p44 contains an RNA recognition motif near its C terminus.

113 domain of CstF-64 showed how the N-terminal RNA recognition motif of CstF-64 recognizes GU-rich RNAs

114 nding sites were mapped to the non-canonical RNA recognition motif of eIF3b and a central 11-amino ac

115 Unexpectedly, deleting the third RNA recognition motif of HuD, the domain that binds the

116 titor, or abrogated by deletion of the third RNA recognition motif of HuR.

117 e phenotype resulting from a mutation in the RNA recognition motif of Nab3.

118 We show that the C-terminal RNA recognition motif of p65, a U12 snRNA binding protei

119 in the serine- and arginine-rich domain and RNA recognition motif of PGC-1 interfere with the abilit

120 s a ribosomopathy caused by a mutation in an RNA recognition motif of RBM28, a nucleolar protein cons

121 ent of the Setd1A complex interacts with the RNA recognition motif of Setd1A and additionally binds t

122 nerated a mouse with a point mutation in the RNA recognition motif of the Nup35 gene, which encodes a

123 ins were upregulated through deletion of the RNA Recognition Motif of the splicing factor RBM20 (Rbm2

124 apping regions containing the NH(2)-terminal RNA recognition motifs of ACF.

125 All three RNA recognition motifs of Hu proteins are required for t

126 The RNA recognition motifs of TIA-1 are linked to a glutamin

127 on-sequential 2-1-3 arrangement of the three RNA recognition motifs on UGU sites in a 5' to 3' orient

128 The RNA recognition motif (or RRM) is a ubiquitous RNA-bindi

129 ntrast, the C-terminal domain containing the RNA recognition motif plays a critical role in the silen

130 RNPS1 is conserved in metazoans and has an RNA-recognition motif preceded by an extensive serine-ri

131 odel and indicate that C protein's canonical RNA recognition motifs probably function in tetramer-tet

132 Binding of RNA to the RNA recognition motifs protects against dephosphorylatio

133 overgrowth dependent on reduced abundance of RNA recognition motif protein Hfp/FIR, which transcripti

134 ires the CCCH zinc-finger protein MEX-5, the RNA Recognition Motif protein SPN-4, and the kinase PAR-

135 -6, a CCCH zinc-finger protein, or SPN-4, an RNA recognition motif protein, causes PAL-1 to be expres

136 URIDYLATE BINDING PROTEIN 1 (UBP1), a triple RNA Recognition Motif protein, in dynamic and reversible

137 FOX-1, an RNA recognition motif protein, triggers hermaphrodite de

138 Loss-of-function mutations in ORGANELLE RNA RECOGNITION MOTIF PROTEIN6 (ORRM6) result in the nea

139 we report that mutant mice lacking TIAR, an RNA recognition motif/ribonucleoprotein-type RNA-binding

140 f RNA-binding proteins harboring a canonical RNA recognition motif (RRM) and a putative prion domain.

141 des a protein that contains two copies of an RNA recognition motif (RRM) and affects alternative RNA

142 The fatty acid binds to the N-terminal RNA Recognition Motif (RRM) and induces a conformational

143 15p is an essential protein that contains an RNA recognition motif (RRM) and localizes to the nucleop

144 wever, AlkB homolog 8 (ABH8), which contains RNA recognition motif (RRM) and methyltransferase domain

145 ich protein 1), contains a single N-terminal RNA recognition motif (RRM) and single C-terminal glycin

146 amily member, the encoded protein carries an RNA recognition motif (RRM) at its C terminus and has th

147 RNA-binding domain of CstF-64 containing an RNA recognition motif (RRM) augmented by N- and C-termin

148 The RNA recognition motif (RRM) binds to single-stranded RNA

149 RNA recognition by CFIA is mediated by an RNA recognition motif (RRM) contained in the Rna15 subun

150 modular organization featuring at least one RNA recognition motif (RRM) domain and a carboxyl-termin

151 uitment, whereas the glycine-rich domain and RNA recognition motif (RRM) domain have a minor contribu

152 es, W105, R107, and L108, interface with the RNA recognition motif (RRM) domain of Aly/REF.

153 association of beta-strands from the single RNA recognition motif (RRM) domain of each subunit.

154 ous kinetic investigations of the N-terminal RNA Recognition Motif (RRM) domain of spliceosomal A pro

155 ous kinetic investigations of the N-terminal RNA recognition motif (RRM) domain of spliceosomal prote

156 The S1 domain protein SRRP1 and two RNA Recognition Motif (RRM) domain proteins, CP33C and C

157 the RS1 and RS2 domains of SR45, and not the RNA recognition motif (RRM) domain, associate independen

158 ort here the solution structure of the eIF4B RNA recognition motif (RRM) domain.

159 forms a complex with SLIRP that harbours an RNA recognition motif (RRM) domain.

160 he SRA1p protein was suggested to contain an RNA recognition motif (RRM) domain.

161 opically expressed miR-574-3p binds multiple RNA recognition motif (RRM) domains of hnRNP L, synergiz

162 ucture of the 34 -kDa ternary complex of the RNA recognition motif (RRM) domains of Hrp1 and Rna15 bo

163 We have investigated how the four RNA recognition motif (RRM) domains of Polypyrimidine tr

164 disordered linker region connecting the two RNA recognition motif (RRM) domains of U2AF2 mediates au

165 mors has an N-terminal deletion (lacking two RNA recognition motif (RRM) domains) and is therefore mi

166 ssential splicing factor Prp24 contains four RNA Recognition Motif (RRM) domains, and functions to an

167 They contain two RNA recognition motif (RRM) domains, which recognize a d

168 roteins associated with AtMSI4 have distinct RNA recognition motif (RRM) domains, which we determined

169 ely related protein TIA-1 are members of the RNA recognition motif (RRM) family of RNA binding protei

170 n identified CUS2, an atypical member of the RNA recognition motif (RRM) family of RNA binding protei

171 ture of nuclear PABPs (PABPNs) with a single RNA recognition motif (RRM) flanked by an acidic N-termi

172 is showing that the IDN2 XS domain adopts an RNA recognition motif (RRM) fold.

173 which has a topology similar to that of the RNA recognition motif (RRM) found in many RNA-binding pr

174 terminal domain (NTD) also interact with the RNA recognition motif (RRM) in b/Prt1, and mutations in

175 east protein of unknown function that has an RNA recognition motif (RRM) in its carboxyl half and a p

176 the canonical RNA-binding surface of the Y14 RNA recognition motif (RRM) is involved in extensive pro

177 The RNA recognition motif (RRM) is one of the most common eu

178 The RNA recognition motif (RRM) is the most abundant RNA-bin

179 atic residues upon binding their targets.The RNA Recognition Motif (RRM) is the most ubiquitous RNA b

180 The protein contains one amino-terminal RNA recognition motif (RRM) known to bind uridine (U)-ri

181 Here, we report a mutation in the RNA recognition motif (RRM) of CSTF2 that changes an asp

182 me product, including homology to a putative RNA recognition motif (RRM) of Ebs1.

183 The RNA recognition motif (RRM) of eIF3 subunit PRT1 interac

184 Mice in which the RNA recognition motif (RRM) of one of the RNA binding mo

185 ved among vertebrates, with glutamine in the RNA recognition motif (RRM) of recombinant hnRNP C1, sug

186 n recognition strategy, in which an atypical RNA recognition motif (RRM) of U2AF35 and the U2AF65 pol

187 ort that SUP-12, a member of a new family of RNA recognition motif (RRM) proteins, including SEB-4, r

188 The RNA Recognition Motif (RRM) type RNA binding protein Bru

189 AdRSZ21 exhibits a RNA recognition motif (RRM), a CCHC type zinc finger dom

190 he predicted SPN-4 protein contains a single RNA recognition motif (RRM), and belongs to a small subf

191 ning the serine-rich (S) domain, the central RNA recognition motif (RRM), and the C-terminal arginine

192 The RNA recognition motif (RRM), one of the most common RNA

193 volves the N-terminal La domain and adjacent RNA recognition motif (RRM), the mechanisms by which La

194 or studying interactions between RNA and the RNA recognition motif (RRM), which is one of the most co

195 rs, the putative RNA helicase MOV10, and the RNA recognition motif (RRM)-containing protein TNRC6B/KI

196 In this study, a RNA recognition motif (RRM)-containing protein, BmLARK,

197 sex determination in the soma and encodes an RNA recognition motif (RRM)-containing protein.

198 ORRM1 belongs to a distinct clade of RNA Recognition Motif (RRM)-containing proteins, most of

199 ) and indicated that it does not resemble an RNA recognition motif (RRM)-like domain.

200 AF) have revealed two unexpected examples of RNA recognition motif (RRM)-like domains with specialize

201 The orb gene encodes an RNA recognition motif (RRM)-type RNA-binding protein tha

202 loop 5 hydrophobic pocket of the human eIF3b RNA recognition motif (RRM).

203 NA-binding domain: a divergent PUM-HD and an RNA recognition motif (RRM).

204 highly sequence-specific manner, through its RNA recognition motif (RRM).

205 NA processing proteins containing the common RNA recognition motif (RRM).

206 que in having two SR domains separated by an RNA recognition motif (RRM).

207 growth and each contains a single canonical RNA recognition motif (RRM).

208 -interacting domain and two highly conserved RNA recognition motifs (RRM) commonly found in ribonucle

209 We report here the solution structure of the RNA recognition motifs (RRM) domain of free human SRSF2

210 Two consecutive RNA recognition motifs (RRM) of U2AF(65) recognize a pol

211 Three highly conserved aromatic residues in RNA recognition motifs (RRM) participate in stacking int

212 inhibits the binding of proteins containing RNA recognition motifs (RRM) to the conserved terminal l

213 Tandem RNA recognition motifs (RRM)s of U2AF65 recognize polypy

214 The N-terminal RNA-recognition motif (RRM) domain of Cyp33 has been fou

215 PHD3 has been shown to interact with the RNA-recognition motif (RRM) domain of human nuclear Cycl

216 The RNA-recognition motif (RRM) is a common and evolutionari

217 Remarkably, the RNA-recognition motif (RRM) of Set1 is required for H3K4

218 n amino acids 18-184, which also include an "RNA recognition motif" (RRM) (residues 77-184).

219 OH) trailer: although the La motif and first RNA recognition motif (RRM1) are sufficient for high-aff

220 eoproteins uses a phylogenetically conserved RNA recognition motif (RRM1) to bind RNA stemloops in U1

221 f Hu proteins and consists of two N-terminal RNA recognition motifs (RRM1 and -2), a hinge region, an

222 Hu proteins, which consist of two N-terminal RNA recognition motifs (RRM1 and RRM2), a hinge region,

223 The protein has three RNA recognition motifs (RRM1, 2 and 3) with a hinge regi

224 divergent N-terminus, three highly conserved RNA recognition motifs (RRM1, RRM2 and RRM3) and a hinge

225 ABP), a protein that contains four conserved RNA recognition motifs (RRM1-4) and a C-terminal domain,

226 AU-rich elements in diverse RNAs through two RNA-recognition motifs, RRM1 and RRM2, and post-transcri

227 Fragments of TDP-43, composed of the second RNA recognition motif (RRM2) and the disordered C termin

228 Regions of TDP-43 flanking the second RNA recognition motif (RRM2) are efficiently cleaved by

229 ing domain of Pab1p was mapped to its second RNA recognition motif (RRM2) in an in vitro binding assa

230 Fragmentation within the second RNA recognition motif (RRM2) of TDP-43 has been observed

231 bove activities of Pab1p requires its second RNA recognition motif (RRM2).

232 C-terminal fragments containing a truncated RNA-recognition motif (RRM2) and a glycine-rich region.

233 We have investigated the behavior of second RNA-recognition motif (RRM2) of neuropathological protei

234 by the novel geometry of its two C-terminal RNA recognition motifs (RRM3 and RRM4), which interact w

235 ive splicing factor) contains two N-terminal RNA recognition motifs (RRMs) (RRM1 and RRM2) and a 50-r

236 strated that a minimum of the N terminus and RNA recognition motifs (RRMs) 1 and 2 are necessary for

237 to stimulate translation: the interaction of RNA recognition motifs (RRMs) 1 and 2 with eukaryotic in

238 We show that the RNA recognition motifs (RRMs) 3 and 4 of PTB can bind tw

239 R are modular proteins with three N-terminal RNA recognition motifs (RRMs) and a C-terminal glutamine

240 TIA1 contains three RNA recognition motifs (RRMs) and a C-terminal low-compl

241 TIA-1 is composed of three RNA recognition motifs (RRMs) and a glutamine-rich domai

242 ologs are characterized by a distinct set of RNA recognition motifs (RRMs) and a SPOC domain, a highl

243 it ends (Spen), a nuclear protein containing RNA recognition motifs (RRMs) and a SPOC domain, is requ

244 ger RNA splicing protein 24 (Prp24) has four RNA recognition motifs (RRMs) and facilitates U6 RNA bas

245 and its homologues contain two NH2-terminal RNA recognition motifs (RRMs) and four COOH-terminal hnR

246 lysis reveals that MINT has three N-terminal RNA recognition motifs (RRMs) and four nuclear localizat

247 proteins are highly conserved containing two RNA recognition motifs (RRMs) and other domains associat

248 RNA recognition motifs (RRMs) are characterized by highl

249 eins that, like CoAA, contain two N-terminal RNA recognition motifs (RRMs) followed by a C-terminal a

250 e provide the solution structures of its two RNA recognition motifs (RRMs) in complex with short RNA.

251 It contains three highly conserved RNA recognition motifs (RRMs) in the absence of other cl

252 domain organization of two tandemly arrayed RNA recognition motifs (RRMs) near the N terminus, follo

253 Fused with the RNA recognition motifs (RRMs) of Crp79 and green fluores

254 The RNA recognition motifs (RRMs) of hnRNP LL were expressed

255 The N-terminal RNA recognition motifs (RRMs) of PABPC1 are necessary fo

256 that TRAP150 binds a region encompassing the RNA recognition motifs (RRMs) of PSF using a previously

257 The RNA recognition motifs (RRMs) of SF2/ASF are active only

258 termined the crystal structure of the tandem RNA recognition motifs (RRMs) of SXL.

259 he U2AF(65) linker residues between the dual RNA recognition motifs (RRMs) recognize the central nucl

260 embers of the family possess two consecutive RNA recognition motifs (RRMs) separated from a third, ca

261 TNRC4 contains two consecutive N-terminal RNA recognition motifs (RRMs) separated from the C-termi

262 HuR carries three highly conserved RNA recognition motifs (RRMs) whereas RNPC1 carries one.

263 Chlamydomonas reinhardtii that contains two RNA recognition motifs (RRMs) which are commonly found i

264 ortion with no obvious functional motif, two RNA recognition motifs (RRMs), and a cysteine-histidine

265 A-binding domain shows two unusually compact RNA recognition motifs (RRMs), and identifies the RNA re

266 PTB), an RNA binding protein containing four RNA recognition motifs (RRMs), is involved in both pre-m

267 consensus sequence of the pre-mRNA using two RNA recognition motifs (RRMs), the most prevalent class

268 of the ELAV family of proteins contain three RNA recognition motifs (RRMs), which are highly conserve

269 interacts with RNA via its second and third RNA recognition motifs (RRMs), with specificity for U-ri

270 While HuD possesses three RNA recognition motifs (RRMs), ZBP1 contains two RRMs an

271 The TIA-1 polypeptide contains three RNA recognition motifs (RRMs).

272 regulation such as serine/arginine (SR) and RNA recognition motifs (RRMs).

273 CELF1 contains three RNA recognition motifs (RRMs).

274 of PABPC in a manner dependent on the PABPC RNA recognition motifs (RRMs).

275 and Cip2 are cytoplasmic proteins that have RNA recognition motifs (RRMs).

276 as lost following deletion of the C-terminal RNA recognition motifs (RRMs).

277 recruitment to genes in vivo depends on its RNA recognition motifs (RRMs).

278 n arginine-serine-rich (RS) domain and three RNA recognition motifs (RRMs).

279 nce analysis suggests that PTB contains four RNA recognition motifs (RRMs).

280 to a closed conformation of the tandem U2AF2 RNA recognition motifs (RRMs).

281 HuR contains three RNA recognition motifs (RRMs): a tandem RRM1 and 2, foll

282 two functional modules consisting of tandem RNA recognition motifs (RRMs; RRM1-RRM2) and a C-termina

283 are located in the second and third of three RNA-recognition motifs (RRMs) in Prp24 and are predicted

284 ent and distinctive PUF RNA binding domains, RNA-recognition motifs (RRMs), and prion regions.

285 inal domain of human hnRNP A1 containing two RNA-recognition motifs (RRMs), bound to a 12-nucleotide

286 racts were RNA-binding proteins that possess RNA-recognition motifs (RRMs).

287 ing regulators in Eukarya, have two types of RNA-recognition motifs (RRMs): a canonical RRM and a pse

288 es located within and adjacent to the second RNA-recognition motif that contribute to both intra- and

289 t encodes a conserved protein, with multiple RNA recognition motifs, that is related to the yeast pro

290 positively regulates binding of the central RNA recognition motif to an exonic splicing enhancer seq

291 MCDs can synergize with a speckle-associated RNA recognition motif to promote speckle specificity and

292 an abasic sugar residue (Type 2) within the RNA-recognition motif to reveal striking differences in

293 de putative RNA-binding proteins of the RRM (RNA recognition motif) type, and the high degree of cons

294 a15 and Hrp1, interact with the mRNA through RNA recognition motif-type RNA binding motifs.

295 y single or double derivatization with other RNA recognition motifs, which could help in the future d

296 The domain is a cryptic, atypical RNA recognition motif with a disordered C-terminal exten

297 as tRNA synthetases, ribosomal proteins, or RNA recognition motifs with their RNA targets.

298 Also, the presence of an RNA recognition motif within HUMORFU_1 suggests that eIF

299 = 4) with simultaneous binding of all three RNA recognition motifs within a single 15-nt binding ele

300 vitro binding experiments revealed that the RNA-recognition motifs within the SART3 sequence are res