blastp_kegg |
lcl|mdm:103420980
|
6 |
367 |
+ |
362 |
Gaps:55 |
25.08 |
1655 |
55.42 |
1e-132 |
endoribonuclease Dicer homolog 3a-like
|
blastp_kegg |
lcl|pxb:103949659
|
6 |
367 |
+ |
362 |
Gaps:55 |
25.08 |
1655 |
55.42 |
9e-132 |
endoribonuclease Dicer homolog 3a-like
|
blastp_kegg |
lcl|mdm:103455760
|
6 |
367 |
+ |
362 |
Gaps:52 |
25.03 |
1654 |
55.56 |
1e-131 |
endoribonuclease Dicer homolog 3a
|
blastp_kegg |
lcl|cit:102624402
|
6 |
367 |
+ |
362 |
Gaps:56 |
24.92 |
1653 |
56.80 |
2e-126 |
endoribonuclease Dicer homolog 3-like
|
blastp_kegg |
lcl|cic:CICLE_v10007239mg
|
6 |
367 |
+ |
362 |
Gaps:56 |
24.94 |
1652 |
56.07 |
1e-124 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103953044
|
7 |
367 |
+ |
361 |
Gaps:53 |
24.92 |
1653 |
54.37 |
1e-124 |
endoribonuclease Dicer homolog 3a-like
|
blastp_kegg |
lcl|tcc:TCM_037410
|
5 |
367 |
+ |
363 |
Gaps:53 |
25.26 |
1639 |
54.11 |
2e-124 |
Endoribonuclease Dicera putative isoform 2
|
blastp_kegg |
lcl|vvi:100254311
|
6 |
367 |
+ |
362 |
Gaps:59 |
25.06 |
1648 |
56.42 |
2e-124 |
endoribonuclease Dicer homolog 3a-like
|
blastp_kegg |
lcl|csv:101229593
|
6 |
367 |
+ |
362 |
Gaps:58 |
25.38 |
1639 |
54.33 |
8e-119 |
endoribonuclease Dicer homolog 3a-like
|
blastp_kegg |
lcl|cmo:103488578
|
6 |
367 |
+ |
362 |
Gaps:64 |
25.41 |
1645 |
55.50 |
2e-118 |
endoribonuclease Dicer homolog 3
|
blastp_uniprot_sprot |
sp|Q9LXW7|DCL3_ARATH
|
6 |
367 |
+ |
362 |
Gaps:56 |
26.08 |
1580 |
48.54 |
3e-107 |
Endoribonuclease Dicer homolog 3 OS Arabidopsis thaliana GN DCL3 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q5N870|DCL3A_ORYSJ
|
7 |
367 |
+ |
361 |
Gaps:67 |
24.23 |
1651 |
46.25 |
2e-88 |
Endoribonuclease Dicer homolog 3a OS Oryza sativa subsp. japonica GN DCL3A PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7XD96|DCL3B_ORYSJ
|
7 |
367 |
+ |
361 |
Gaps:59 |
24.56 |
1637 |
43.03 |
5e-80 |
Endoribonuclease Dicer homolog 3b OS Oryza sativa subsp. japonica GN DCL3B PE 3 SV 2
|
blastp_uniprot_sprot |
sp|P84634|DCL4_ARATH
|
7 |
368 |
+ |
362 |
Gaps:61 |
22.27 |
1702 |
28.23 |
1e-27 |
Dicer-like protein 4 OS Arabidopsis thaliana GN DCL4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q8LMR2|DCL1_ORYSJ
|
99 |
368 |
+ |
270 |
Gaps:36 |
14.23 |
1883 |
32.46 |
2e-27 |
Endoribonuclease Dicer homolog 1 OS Oryza sativa subsp. japonica GN DCL1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9SP32|DCL1_ARATH
|
180 |
368 |
+ |
189 |
Gaps:12 |
9.38 |
1909 |
37.99 |
3e-26 |
Endoribonuclease Dicer homolog 1 OS Arabidopsis thaliana GN DCL1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|A7LFZ6|DCL4_ORYSJ
|
7 |
368 |
+ |
362 |
Gaps:39 |
22.75 |
1657 |
31.03 |
5e-22 |
Endoribonuclease Dicer homolog 4 OS Oryza sativa subsp. japonica GN DCL4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q69LX2|DCL2B_ORYSJ
|
182 |
366 |
+ |
185 |
Gaps:12 |
13.00 |
1377 |
36.87 |
5e-19 |
Endoribonuclease Dicer homolog 2b OS Oryza sativa subsp. japonica GN DCL2B PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q3EBC8|DCL2_ARATH
|
25 |
409 |
+ |
385 |
Gaps:105 |
28.53 |
1388 |
28.79 |
6e-19 |
Endoribonuclease Dicer homolog 2 OS Arabidopsis thaliana GN At3g03300 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q10HL3|DCL2A_ORYSJ
|
182 |
366 |
+ |
185 |
Gaps:12 |
12.70 |
1410 |
36.87 |
9e-19 |
Endoribonuclease Dicer homolog 2a OS Oryza sativa subsp. japonica GN DCL2A PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|30329
|
126 |
255 |
+ |
130 |
Gaps:25 |
98.52 |
135 |
34.59 |
3e-19 |
cd02844 PAZ_CAF_like PAZ domain CAF_like subfamily. CAF (for carpel factory) is a plant homolog of Dicer. CAF has been implicated in flower morphogenesis and in early Arabidopsis development and might function through posttranscriptional regulation of specific mRNA molecules. PAZ domains are named after the proteins Piwi Argonaut and Zwille. PAZ is found in two families of proteins that are essential components of RNA-mediated gene-silencing pathways including RNA interference the Piwi and Dicer families. PAZ functions as a nucleic-acid binding domain with a strong preference for single-stranded nucleic acids (RNA or DNA) or RNA duplexes with single-stranded 3' overhangs. It has been suggested that the PAZ domain provides a unique mode for the recognition of the two 3'-terminal nucleotides in single-stranded nucleic acids and buries the 3' OH group and that it might recognize characteristic 3' overhangs in siRNAs within RISC (RNA-induced silencing) and other complexes..
|
rpsblast_cdd |
gnl|CDD|29697
|
296 |
367 |
+ |
72 |
Gaps:3 |
56.39 |
133 |
40.00 |
5e-14 |
cd00593 RIBOc RIBOc. Ribonuclease III C terminal domain. This group consists of eukaryotic bacterial and archeal ribonuclease III (RNAse III) proteins. RNAse III is a double stranded RNA-specific endonuclease. Prokaryotic RNAse III is important in post-transcriptional control of mRNA stability and translational efficiency. It is involved in the processing of ribosomal RNA precursors. Prokaryotic RNAse III also plays a role in the maturation of tRNA precursors and in the processing of phage and plasmid transcripts. Eukaryotic RNase III's participate (through direct cleavage) in rRNA processing in processing of small nucleolar RNAs (snoRNAs) and snRNA's (components of the spliceosome). In eukaryotes RNase III or RNaseIII like enzymes such as Dicer are involved in RNAi (RNA interference) and miRNA (micro-RNA) gene silencing..
|
rpsblast_cdd |
gnl|CDD|197778
|
296 |
367 |
+ |
72 |
Gaps:1 |
56.59 |
129 |
38.36 |
3e-13 |
smart00535 RIBOc Ribonuclease III family.
|
rpsblast_cdd |
gnl|CDD|178863
|
296 |
366 |
+ |
71 |
Gaps:10 |
32.75 |
229 |
32.00 |
2e-11 |
PRK00102 rnc ribonuclease III Reviewed.
|
rpsblast_cdd |
gnl|CDD|201363
|
314 |
367 |
+ |
54 |
none |
59.34 |
91 |
40.74 |
1e-08 |
pfam00636 Ribonuclease_3 Ribonuclease III domain.
|
rpsblast_cdd |
gnl|CDD|211723
|
314 |
366 |
+ |
53 |
none |
26.11 |
203 |
37.74 |
4e-08 |
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_cdd |
gnl|CDD|30916
|
314 |
366 |
+ |
53 |
none |
22.55 |
235 |
37.74 |
6e-08 |
COG0571 Rnc dsRNA-specific ribonuclease [Transcription].
|
rpsblast_kog |
gnl|CDD|35920
|
5 |
367 |
+ |
363 |
Gaps:88 |
27.96 |
1606 |
18.71 |
1e-22 |
KOG0701 KOG0701 KOG0701 dsRNA-specific nuclease Dicer and related ribonucleases [RNA processing and modification].
|