ライフサイエンスコーパス: RNA-binding motif

1 ins containing copies of the double-stranded RNA binding motif.

2 ough a region related to the double-stranded RNA binding motif.

3 hus appears to interfere with the N-terminal RNA binding motif.

4 esent a common, but previously unrecognized, RNA binding motif.

5 G boxes have been postulated to represent an RNA binding motif.

6 and in vivo despite its lack of a canonical RNA binding motif.

7 s) contains the unusual CCCH zinc finger, an RNA binding motif.

8 ucture but contains only one double-stranded RNA binding motif.

9 nce homology to any previously characterized RNA binding motif.

10 nd threonyl-tRNA synthetase, reveals a novel RNA-binding motif.

11 ike RNA-binding domains, and an RGG-box type RNA-binding motif.

12 ginine-rich C-terminus reminiscent of an RGG RNA-binding motif.

13 contain two copies of the RRM-type consensus RNA-binding motif.

14 licing regulation, we sought to identify its RNA-binding motif.

15 a remarkably versatile and highly conserved RNA-binding motif.

16 uggests that this protein fold is an ancient RNA-binding motif.

17 ondrial membrane, includes a K homology (KH) RNA-binding motif.

18 tually every clone contained a known DNA- or RNA-binding motif.

19 the mRNA through RNA recognition motif-type RNA binding motifs.

20 localization signal and two double-stranded-RNA binding motifs.

21 is novel and lacks all of the characterized RNA binding motifs.

22 ons, but does not include other recognizable RNA binding motifs.

23 contain three characteristic RNP2/RNP1-type RNA binding motifs.

24 AMV coat protein lacks previously identified RNA binding motifs.

25 P-granule component in lacking recognizable RNA binding motifs.

26 ine-polycytidylic acid via its double-strand RNA binding motifs.

27 s appear to form a novel gene family sharing RNA-binding motifs.

28 transcriptase domain but retaining the known RNA-binding motifs.

29 ic modifiers that bind RNA without canonical RNA-binding motifs.

30 It interacts with NF90's double-stranded RNA-binding motifs.

31 y mutations in the RBM10 gene, which encodes RNA binding motif 10.

32 RSF1, we showed that several residues in the RNA-binding motif 2 interact with the N-terminal region

33 Disruption of the implicated intramolecular RNA-binding motif 2-RS domain interaction impairs both t

34 The splicing factor RNA-binding motif 20 (RBM20) regulates the contour lengt

35 he RNA recognition motif (RRM) of one of the RNA binding motif-20 alleles was floxed and that express

36 Inhibition of the RNA binding motif-20-based titin splicing system upregul

37 ly through inhibition of the splicing factor RNA binding motif-20.

38 g sequences identified a novel fusion of the RNA binding motif 6 (RBM6) gene to CSF1R gene generated

39 tely 120 amino acids forming another type of RNA binding motif, a RGG box.

40 d by the LIN-28 protein's unusual pairing of RNA-binding motifs: a cold shock domain (CSD) and a pair

41 1 to 200, but not R312A substitution in the RNA binding motif, abolished the ability of the VP35 pro

42 In addition, yeast Nep1 binds to a 6-nt RNA-binding motif also found in 18S rRNA and facilitates

43 Mutations in the eIF3c RNA-binding motif also reduce 40S ribosomal subunit bind

44 dsRNA binding motifs, or the isolated first RNA binding motif (amino acids 1-123).

45 The conservation of the RNA binding motifs among Y-box protein family members ra

46 contain two copies of a double-stranded (ds) RNA binding motif and bind strongly to dsRNA.

47 RBMS3 contains two pairs of RNA binding motifs and is very closely related to the st

48 though a HEXIM1 dimer contains two potential RNA binding motifs and ultimately recruits two P-TEFb mo

49 th an autosomal hnRNPG gene that contains an RNA-binding motif and one of the four SRGY repeats found

50 e large proteins characterized by N-terminal RNA-binding motifs and a highly conserved C-terminal SPO

51 ive-helix bundle that is distinct from known RNA-binding motifs and instead is similar to the carboxy

52 DSEF-1 protein contains three RNA-binding motifs and is a member of the hnRNP H family

53 t differ in the number of tandem zinc-finger RNA-binding motifs and subcellular localization, is expr

54 at does not contain any previously described RNA-binding motifs and that contains only 2 of the 11 pr

55 which consists of two tandem double-stranded RNA binding motifs, and a C-terminal kinase domain.

56 ly related proteins that contain a predicted RNA-binding motif, and both loci are expressed exclusive

57 terminus to include a single double-stranded RNA-binding motif, and that T20H4.4 occupies the second

58 inal region, consisting of a double-stranded RNA-binding motif, and the N-terminal region (vZ(E3L)),

59 Y chromosome that encode proteins containing RNA-binding motifs, and both have been described as cand

60 no acid sequence contains four arginine-rich RNA-binding motifs, and one segment shows strong homolog

61 inal domain, containing a number of putative RNA-binding motifs, and the catalytic function of the ca

62 However, the RNA binding motifs are not sufficient for trans-activati

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

64 apsid protein (CP) contains an arginine-rich RNA binding motif (ARM) that is also found in the CPs of

65 RNA-binding peptides using the arginine-rich RNA-binding motif as a framework.

66 ossess functionally distinct double-stranded RNA-binding motifs as measured with synthetic double-str

67 g ATP hydrolysis in the presence of specific RNA binding motifs (AUUUA) of cyclin D1 mRNA.

68 are similar in fold to previously identified RNA binding motifs, despite limited sequence homology.

69 complex and contains a double-stranded (ds)-RNA-binding motif (DRM).

70 cid residues within the double-stranded (ds) RNA binding motif (dsRBM) of the vaccinia virus E3 prote

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

72 tandem copies of a conserved double-stranded RNA binding motif, dsRBM1 and dsRBM2.

73 g protein, NF90 contains two double stranded RNA-binding motifs (dsRBMs) and interacts with highly st

74 ADAR2 contains two tandem double-stranded RNA-binding motifs (dsRBMs) that are not only important

75 ot the other, of ADAR2's two double-stranded RNA-binding motifs (dsRBMs), and the correct placement o

76 efined by the presence of a highly conserved RNA binding motif first described in the mei2 gene of th

77 ed residues reminiscent of the arginine-rich RNA-binding motif found in a wide variety of proteins.

78 mino acids of RH II/Gu can be replaced by an RNA binding motif from nucleolar protein p120 without a

79 The RBM (RNA-binding motif) gene family on the human Y chromosome

80 and the larger ones remove some of the RBM (RNA Binding Motif) genes, but none of the deletion males

81 gosaccharide-binding (OB) fold is a ssDNA or RNA binding motif in prokaryotes and eukaryotes.

82 in agreement with the presence of a putative RNA binding motif in the deduced amino acid sequence.

83 of protein-RNA interactions, defined by four RNA binding motifs in RNase III and three protein-intera

84 Part of it is highly homologous to the TAR RNA-binding motif in the human immunodeficiency virus ty

85 xperiments, we identify two highly conserved RNA-binding motifs in eIF3 that direct translation initi

86 ese findings suggest that individual KH-like RNA-binding motifs in ICP27 may be involved in binding d

87 RNA profiling and bioinformatics to identify RNA-binding motifs in mRNAs that either enter or exit th

88 dered domains adjacent to well characterized RNA-binding motifs in other promiscuous RNA-binding prot

89 possible biological significance of putative RNA-binding motifs in the N and palm domains of RB69 gp4

90 ractions with basic residues and Cys-His box RNA-binding motifs in the nucleocapsid.

91 apart, matching the distance between the two RNA-binding motifs in the Rev dimer.

92 rich (RS) domain but does not have any known RNA-binding motifs, indicating that it is not a member o

93 editing catalytic polypeptide 3 family) have RNA-binding motifs, invade assembling human immunodefici

94 A PTBP2 consensus RNA binding motif is enriched in the TDP-43 RIP-seq libr

95 The arginine-rich RNA binding motif is found in a wide variety of proteins

96 rther reveals that the suggested nucleoporin RNA binding motif is unlikely to bind to RNA.

97 which contains two putative double-stranded RNA binding motifs, is essential for the in vivo functio

98 tact cold-shock domain (CSD), containing two RNA-binding motifs, is required to localize MSY2 to the

99 predicted alpha and beta structures of this RNA binding motif lack who function.

100 All three RNA-binding motifs (LAM, RRM1, and RRM2) of La/SSB are r

101 a CLIP-seq experiment, we find that EWS-FLI1 RNA-binding motifs most frequently occur adjacent to int

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

103 tein with a loss-of-function mutation in the RNA-binding motif no longer binds to the mRNA cap struct

104 This analysis has identified a unique RNA binding motif of alternating basic and aromatic resi

105 The helix-loop groove RNA binding motif of T4 RegA protein is fully conserved

106 differs from the (A-R-N) tripartite poly(A) RNA-binding motif of Escherichia coli Hfq whereby the Sa

107 HDV RNA, indicating that both the NLS and an RNA-binding motif of HDAg are required for the RNA-trans

108 Mutations in the RNA-binding motif of subunit eIF3a weaken eIF3 binding t

109 However, the RNA-binding motif of Uap56p is critical for nuclear expo

110 e functional importance of each of the three RNA-binding motifs of ADAR1 varied with the specific tar

111 of the nuclear localization signal (NLS) or RNA-binding motifs of HDAg resulted in the failure of nu

112 eraction that enlists both of the N-terminal RNA-binding motifs of the protein with separate surfaces

113 The structure reveals a bipartite RNA-binding motif on the distal face that is composed of

114 e discovery of oncogenic activation of RBMY (RNA-binding motif on Y chromosome), which is absent in n

115 Dom34p contains an RNA binding motif present in several ribosomal proteins

116 l analysis of the three double-stranded (ds) RNA binding motifs present in ADAR1 revealed a different

117 ntaining octamer-binding protein (NONO), and RNA binding motif protein 14 (RBM14), all reported to be

118 ss-of-function mutation in the gene encoding RNA binding motif protein 20 (Rbm20) as the underlying c

119 RNA binding motif protein 25 (RBM25) is a putative splic

120 hat associates with the core splicing factor RNA binding motif protein 39 (RBM39) and localizes to nu

121 d bestrophin 1 (BEST1), transcription factor RNA binding motif protein 39 (RBM39), inflammatory media

122 indisulam promotes the recruitment of RBM39 (RNA binding motif protein 39) to the CUL4-DCAF15 E3 ubiq

123 r genome resequencing studies, we identified RNA binding motif protein 47 (RBM47) as a suppressor of

124 exon 9 of RBM20, encoding ribonucleic acid (RNA) binding motif protein 20.

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

126 RNA-binding motif protein 15 (RBM15) is involved in the

127 RNA-binding motif protein 20 (RBM20) is essential for no

128 zygous missense mutations were identified in RNA-binding motif protein 20 (RBM20), a spliceosome prot

129 n of several cardiac splice factors, such as RNA-binding motif protein 20 and SF3B1, not only provide

130 inate lyase, neuronal nitric-oxide synthase, RNA-binding motif protein 3, peroxiredoxin I, proteasome

131 RNA-binding motif protein 38 (Rbm38), also called RNPC1

132 to result in the fusion of two novel genes, RNA-binding motif protein-15 (RBM15), an RNA recognition

133 finity despite the absence of a recognizable RNA binding motif (RBM).

134 An RNA-binding motif (RBM) gene family has been identified

135 RNA-binding motif (RBM) genes are found on all mammalian

136 ars to be a new member of a highly conserved RNA-binding motif (RBM) protein family that is highly co

137 ular biology through binding single-stranded RNA binding motifs (RBMs).

138 The fusilli gene encodes a protein with RNA binding motifs related to those in mammalian hnRNP F

139 ur understanding of binding partners and PAN RNA binding motifs remains incomplete.

140 Two RNA-binding motifs, RI and RII, were present in exons 4

141 WhGRP-1 contains two conserved domains, the RNA-binding motif (RNP motif) combined with a series of

142 Within this domain are two highly conserved RNA-binding motifs, RNP-1 and RNP-2.

143 tranded beta-barrel structure containing two RNA-binding motifs, RNP1 and RNP2.

144 ine and histidine residues that resemble the RNA binding motifs seen in some other proteins.

145 ion of the HIF1A inhibitor YC1 (now known as RNA-binding motif, single-stranded-interacting protein 1

146 in components of P granules contain putative RNA-binding motifs, suggesting that RNA is involved in e

147 ead association between polyQ expansions and RNA-binding motifs, suggesting that this is a broadly ex

148 h p33, contain an arginine- and proline-rich RNA-binding motif (termed RPR, which has the sequence RP

149 KH domains are RNA binding motifs that usually occur in tandem repeats

150 The K homology (KH) module is a widespread RNA-binding motif that has been detected by sequence sim

151 , we identified a highly conserved, putative RNA-binding motif that is critical for PRF transactivati

152 purred the evolution of diverse noncanonical RNA-binding motifs that perform organelle-specific funct

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

154 ose that this betaalphaalphabeta fold is the RNA binding motif, the minimum structural requirement fo

155 lthough both contain the consensus VIGxxGxxI RNA-binding motif, the protein folds are probably differ

156 FMRP is methylated on the high-affinity RNA-binding motif, the RGG box, at positions 533, 538, 5

157 The 62-kD protein contained two types of RNA-binding motifs, the consensus sequence RNA-binding d

158 TUTases have C-terminal folds reminiscent of RNA binding motifs, thus indicating the presence of nume

159 The similarity of these R2 RNA binding motifs to those of telomerase and group II i

160 n HEXIM1 C-terminal to its previously mapped RNA-binding motif was also required for interactions bet

161 , any one of the three previously identified RNA-binding motifs was sufficient to confer the RNA-tran

162 27 N-terminal peptide, including the RGG box RNA binding motif, was expressed and its binding specifi

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

164 nserved amino acids throughout the SBP2 L7Ae RNA binding motif were mutated to alanine in clusters of

165 orts viral RNA through an N-terminal RGG box RNA binding motif, which is necessary and sufficient for

166 es N-7 pol may be structurally related to an RNA-binding motif, which appears to be conserved among a

167 Six gene families, including RBMY (RNA binding motif, Y chromosome), DAZ (deleted in azoosp

168 The RBMY (RNA-binding motif, Y chromosome) gene family encodes a g