blastp_kegg |
lcl|pop:POPTR_0017s09580g
|
7 |
488 |
+ |
482 |
Gaps:30 |
98.97 |
487 |
70.95 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_017279
|
7 |
488 |
+ |
482 |
Gaps:23 |
100.00 |
497 |
69.42 |
0.0 |
DsRNA-binding protein 3 isoform 1
|
blastp_kegg |
lcl|vvi:100254871
|
4 |
488 |
+ |
485 |
Gaps:23 |
100.00 |
484 |
69.83 |
0.0 |
double-stranded RNA-binding protein 5-like
|
blastp_kegg |
lcl|pmum:103330294
|
7 |
488 |
+ |
482 |
Gaps:79 |
98.13 |
482 |
70.61 |
0.0 |
double-stranded RNA-binding protein 3
|
blastp_kegg |
lcl|cit:102607899
|
7 |
488 |
+ |
482 |
Gaps:41 |
100.00 |
473 |
65.96 |
3e-180 |
double-stranded RNA-binding protein 3-like
|
blastp_kegg |
lcl|mdm:103421440
|
7 |
488 |
+ |
482 |
Gaps:46 |
97.72 |
483 |
65.68 |
9e-179 |
double-stranded RNA-binding protein 5-like
|
blastp_kegg |
lcl|mdm:103442108
|
7 |
488 |
+ |
482 |
Gaps:46 |
97.72 |
483 |
65.68 |
9e-179 |
double-stranded RNA-binding protein 5-like
|
blastp_kegg |
lcl|pxb:103938515
|
7 |
488 |
+ |
482 |
Gaps:59 |
97.80 |
500 |
63.80 |
1e-178 |
double-stranded RNA-binding protein 3-like
|
blastp_kegg |
lcl|rcu:RCOM_1446760
|
4 |
488 |
+ |
485 |
Gaps:46 |
100.00 |
477 |
65.62 |
7e-166 |
double-stranded RNA binding protein putative
|
blastp_kegg |
lcl|fve:101308997
|
7 |
446 |
+ |
440 |
Gaps:71 |
96.12 |
490 |
60.72 |
1e-163 |
double-stranded RNA-binding protein 5-like
|
blastp_pdb |
2l2m_A
|
88 |
160 |
+ |
73 |
Gaps:1 |
96.10 |
77 |
41.89 |
1e-09 |
mol:protein length:77 Hyponastic leave 1
|
blastp_pdb |
3adj_A
|
92 |
160 |
+ |
69 |
Gaps:1 |
92.11 |
76 |
41.43 |
5e-08 |
mol:protein length:76 F21M12.9 protein
|
blastp_uniprot_sprot |
sp|Q8GY79|DRB5_ARATH
|
7 |
275 |
+ |
269 |
Gaps:29 |
64.63 |
393 |
68.50 |
1e-103 |
Double-stranded RNA-binding protein 5 OS Arabidopsis thaliana GN DRB5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LJF5|DRB3_ARATH
|
7 |
208 |
+ |
202 |
Gaps:10 |
53.48 |
359 |
77.08 |
1e-101 |
Double-stranded RNA-binding protein 3 OS Arabidopsis thaliana GN DRB3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q0DKP4|DRB2_ORYSJ
|
7 |
211 |
+ |
205 |
Gaps:3 |
35.08 |
593 |
68.27 |
1e-93 |
Double-stranded RNA-binding protein 2 OS Oryza sativa subsp. japonica GN DRB2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SKN2|DRB2_ARATH
|
7 |
197 |
+ |
191 |
none |
44.01 |
434 |
69.11 |
4e-88 |
Double-stranded RNA-binding protein 2 OS Arabidopsis thaliana GN DRB2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|B7E321|DRB5_ORYSJ
|
7 |
161 |
+ |
155 |
none |
38.37 |
404 |
81.94 |
6e-86 |
Double-stranded RNA-binding protein 5 OS Oryza sativa subsp. japonica GN DRB5 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9AV50|DRB6_ORYSJ
|
7 |
200 |
+ |
194 |
none |
37.74 |
514 |
68.04 |
9e-77 |
Double-stranded RNA-binding protein 6 OS Oryza sativa subsp. japonica GN DRB6 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8H1D4|DRB4_ARATH
|
4 |
160 |
+ |
157 |
Gaps:8 |
41.97 |
355 |
50.34 |
2e-34 |
Double-stranded RNA-binding protein 4 OS Arabidopsis thaliana GN DBR4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q5N8Z0|DRB1_ORYSJ
|
7 |
159 |
+ |
153 |
Gaps:7 |
52.61 |
441 |
45.26 |
1e-30 |
Double-stranded RNA-binding protein 1 OS Oryza sativa subsp. japonica GN DRB1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q0IQN6|DRB8_ORYSJ
|
7 |
160 |
+ |
154 |
Gaps:2 |
35.85 |
424 |
40.79 |
2e-24 |
Double-stranded RNA-binding protein 8 OS Oryza sativa subsp. japonica GN DRB8 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q0IV63|DRB7_ORYSJ
|
7 |
160 |
+ |
154 |
Gaps:2 |
32.14 |
473 |
40.79 |
4e-24 |
Double-stranded RNA-binding protein 7 OS Oryza sativa subsp. japonica GN DRB7 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|200945
|
8 |
159 |
+ |
152 |
Gaps:1 |
100.00 |
66 |
43.94 |
3e-13 |
pfam00035 dsrm Double-stranded RNA binding motif. Sequences gathered for seed by HMM_iterative_training Putative motif shared by proteins that bind to dsRNA. At least some DSRM proteins seem to bind to specific RNA targets. Exemplified by Staufen which is involved in localisation of at least five different mRNAs in the early Drosophila embryo. Also by interferon-induced protein kinase in humans which is part of the cellular response to dsRNA.
|
rpsblast_cdd |
gnl|CDD|28930
|
8 |
159 |
+ |
152 |
Gaps:3 |
98.53 |
68 |
53.73 |
2e-12 |
cd00048 DSRM Double-stranded RNA binding motif. Binding is not sequence specific but is highly specific for double stranded RNA. Found in a variety of proteins including dsRNA dependent protein kinase PKR RNA helicases Drosophila staufen protein E. coli RNase III RNases H1 and dsRNA dependent adenosine deaminases..
|
rpsblast_cdd |
gnl|CDD|178863
|
8 |
162 |
+ |
155 |
Gaps:13 |
41.48 |
229 |
43.16 |
3e-12 |
PRK00102 rnc ribonuclease III Reviewed.
|
rpsblast_cdd |
gnl|CDD|197679
|
8 |
160 |
+ |
153 |
Gaps:7 |
100.00 |
67 |
55.22 |
1e-10 |
smart00358 DSRM Double-stranded RNA binding motif.
|
rpsblast_cdd |
gnl|CDD|30916
|
8 |
165 |
+ |
158 |
Gaps:3 |
31.06 |
235 |
43.84 |
6e-08 |
COG0571 Rnc dsRNA-specific ribonuclease [Transcription].
|
rpsblast_cdd |
gnl|CDD|211723
|
8 |
52 |
+ |
45 |
Gaps:1 |
22.66 |
203 |
43.48 |
3e-07 |
TIGR02191 RNaseIII ribonuclease III bacterial. This family consists of bacterial examples of ribonuclease III. This enzyme cleaves double-stranded rRNA. It is involved in processing ribosomal RNA precursors. It is found even in minimal genones such as Mycoplasma genitalium and Buchnera aphidicola and in some cases has been shown to be an essential gene. These bacterial proteins contain a double-stranded RNA binding motif (pfam00035) and a ribonuclease III domain (pfam00636). Eukaryotic homologs tend to be much longer proteins with additional domains localized to the nucleus and not included in this family.
|
rpsblast_kog |
gnl|CDD|38936
|
58 |
163 |
+ |
106 |
Gaps:7 |
30.97 |
339 |
42.86 |
5e-07 |
KOG3732 KOG3732 KOG3732 Staufen and related double-stranded-RNA-binding proteins [Intracellular trafficking secretion and vesicular transport Transcription].
|