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 is inserted near the beginning of the second RNA recognition motif.

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

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

14 -269 TDP-43 fragment, which comprise the two RNA recognition motifs.

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

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

17 ated splicing factors that possess identical RNA recognition motifs.

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

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

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

21 kDa protein that contains three nonidentical RNA recognition motifs.

22 ich are characterized by the presence of two RNA recognition motifs.

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

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

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

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

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

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

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

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

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

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

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

36 genes encode proteins that contain a single RNA recognition motif and a (different) internally repea

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

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

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

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

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

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

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

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

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

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

50 arboxyl-terminal half of Nopp52 contains two RNA recognition motifs and an extreme carboxyl-terminal

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 olins, including an N-terminal acidic motif, RNA recognition motifs, and a C-terminal Gly- and Arg-ri

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

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

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

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

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

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

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

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

65 are abrogated by mutation of the N-terminal RNA recognition motif but are not affected by mutation o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Like most SR proteins, B52 contains two RNA recognition motifs in the N terminus and a C-termina

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

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

104 A novel RNA recognition motif is characterized in an arginine-ri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Finally, we demonstrated that both RNA recognition motifs of B52 are required for RNA bindi

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

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

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

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

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

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

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

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

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

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

137 -6, a CCCH zinc-finger protein, or SPN-4, an RNA recognition motif protein, causes PAL-1 to be expres

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

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

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

141 ain, the ribonucleoprotein motifs within the RNA recognition motif RNA binding domain, and the SR dom

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

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

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

145 15p is an essential protein that contains an RNA recognition motif (RRM) and localizes to the nucleop

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

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

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

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

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

151 odes an essential RNA-binding protein of the RNA recognition motif (RRM) class that is required durin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 cesses have a common RNA binding domain, the RNA recognition motif (RRM).

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

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

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

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

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

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

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

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

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

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

217 NONA polypeptide contains two copies of the RNA-recognition motif (RRM), a hallmark of proteins invo

218 TIA-1 that is immunochemically related to an RNA-recognition motif (RRM)-type RNA-binding protein des

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Nop4p is unusual in that it contains four RNA recognition motifs (RRMs) including one noncanonical

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

272 CELF1 contains three RNA recognition motifs (RRMs).

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

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

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

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

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

278 nding protein that contains two nonidentical RNA recognition motifs (RRMs).

279 oly(A)-binding protein (Pab1p) contains four RNA recognition motifs (RRMs).

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

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

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

283 odular structure that consists of one or two RNA-recognition motifs (RRMs) and a COOH-terminal argini

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

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

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

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

288 f RNA-binding proteins that have one or more RNA-recognition motifs (RRMs).

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

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

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

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

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

294 g factors, which have in common a N-terminal RNA recognition motif-type RNA binding domain, a Gly-ric

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

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

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

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

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

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