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1 terminus of E3L, which contains a conserved double-stranded RNA binding domain.
2 ated in the NTR was identified as a putative double-stranded RNA-binding domain.
3 exacerbated by K51A substitution in the Tat double-stranded RNA-binding domain.
4 se H fold, whereas HicA (COG1724) contains a double-stranded RNA-binding domain.
5 ster of basic residues followed by the third double-stranded RNA-binding domain.
6 Prbp contains two copies of a double-stranded-RNA-binding domain.
7 UF283) found in Dicer proteins is related to double-stranded RNA-binding domains.
8 that disrupt the Dicer ribonuclease III and double-stranded RNA-binding domains.
9 not when overexpressing mutant ADAR1 lacking double-stranded RNA-binding domains.
10 n, visinin-like protein (VILIP) contains one double-stranded RNA-binding domain, a protein motif cons
11 econd entails nonspecific RNA binding by the double-stranded RNA binding domain, an interaction that
12 propose that bivalent interactions with the double stranded RNA binding domain and the basic region
13 NAs also activate PKR constructs lacking the double-stranded RNA binding domain and bind to a basic r
14 ovel transcriptional repressor harboring two double-stranded RNA-binding domains and a region homolog
15 ne residues in the distal alpha-helix of the double-stranded RNA-binding domains are necessary to eng
16 is flanked by two alpha-beta-beta-beta-alpha double-stranded RNA-binding domains at the N terminus an
17 profile comparisons, we detected a divergent double-stranded RNA-binding domain coinciding with the D
18 mbles the alphabetabetabetaalpha topology of double-stranded RNA-binding domains, despite limited seq
20 o induce translation: the first includes the double-stranded RNA binding domains (DRBMs) of ADAR1 whi
21 ap in a RanGTP-dependent manner and that its double-stranded RNA binding domain (dsRBD) is the limiti
22 res of known RNA binding domains such as the double-stranded RNA binding domain (dsRBD), the hnRNP K
23 binding activities, both of which required a double-stranded RNA-binding domain (dsRBD) and a functio
25 fold, via shape-specific interactions by its double-stranded RNA-binding domain (dsRBD) helix alpha1
26 t structural relatives are proteins with the double-stranded RNA-binding domain (dsRBD) motif althoug
27 N-terminal nuclease domain and a C-terminal double-stranded RNA-binding domain (dsRBD), and are acti
32 the nonsequence-specific protein TRBP, whose double-stranded RNA-binding domains (dsRBDs) interact wi
37 e RNA-binding protein), which contains three double-stranded, RNA-binding domains, is an integral com
38 served lentivirus Vif motif was found in the double-stranded RNA binding domain of Xenopus laevis, Xl
39 ng at the Q/R site of GRIA2 Furthermore, the double-stranded RNA binding domains of ADAR3 are require
40 ith pre-60S ribosomal particles requires the double-stranded RNA binding domains of NF90, while deple
42 effect is critically dependent on the third double-stranded RNA-binding domain of Staufen1 and shutt
43 These data support the hypothesis that the double-stranded RNA-binding domains of this family of pr
45 , III, II and PH and D families as well as a double-stranded RNA binding domain present in RNase III.
46 nd mass spectrometry, we have identified the double-stranded RNA-binding domain protein Blanks to be
47 ists of the nuclear RNase III Drosha and the double-stranded RNA-binding domain protein DGCR8 (DiGeor
48 oach that uses a peptide transduction domain-double-stranded RNA-binding domain (PTD-DRBD) fusion pro
49 identify a region of CBTF122 containing the double-stranded RNA-binding domains that is capable of b
52 esis or the introduction of mutations in the double-stranded RNA-binding domains within ADAR2 results
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