blastp_kegg |
lcl|tcc:TCM_037118
|
13 |
367 |
+ |
355 |
Gaps:15 |
21.78 |
1690 |
63.86 |
2e-138 |
Dicer-like protein isoform 2
|
blastp_kegg |
lcl|cic:CICLE_v10007241mg
|
15 |
365 |
+ |
351 |
Gaps:15 |
22.76 |
1564 |
62.92 |
7e-135 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102621372
|
15 |
365 |
+ |
351 |
Gaps:15 |
21.55 |
1652 |
62.64 |
4e-134 |
dicer-like protein 4-like
|
blastp_kegg |
lcl|vvi:100243116
|
13 |
365 |
+ |
353 |
Gaps:11 |
21.95 |
1622 |
63.48 |
6e-134 |
dicer-like protein 4
|
blastp_kegg |
lcl|pop:POPTR_0006s20310g
|
13 |
362 |
+ |
350 |
Gaps:14 |
21.73 |
1638 |
62.36 |
1e-133 |
POPTRDRAFT_802171 hypothetical protein
|
blastp_kegg |
lcl|mdm:103400333
|
2 |
367 |
+ |
366 |
Gaps:25 |
31.31 |
1185 |
59.84 |
4e-130 |
dicer-like protein 4
|
blastp_kegg |
lcl|rcu:RCOM_0701500
|
13 |
362 |
+ |
350 |
Gaps:17 |
21.62 |
1633 |
61.47 |
3e-127 |
Ribonuclease III putative (EC:3.1.26.3)
|
blastp_kegg |
lcl|pxb:103949123
|
2 |
367 |
+ |
366 |
Gaps:25 |
22.84 |
1624 |
60.11 |
2e-126 |
dicer-like protein 4
|
blastp_kegg |
lcl|pmum:103341363
|
2 |
367 |
+ |
366 |
Gaps:20 |
22.66 |
1659 |
59.84 |
9e-125 |
dicer-like protein 4
|
blastp_kegg |
lcl|pper:PRUPE_ppa000144mg
|
2 |
367 |
+ |
366 |
Gaps:20 |
22.94 |
1639 |
59.57 |
2e-124 |
hypothetical protein
|
blastp_pdb |
2kou_A
|
2 |
83 |
+ |
82 |
none |
80.39 |
102 |
45.12 |
3e-14 |
mol:protein length:102 Dicer-like protein 4
|
blastp_uniprot_sprot |
sp|P84634|DCL4_ARATH
|
2 |
369 |
+ |
368 |
Gaps:17 |
22.50 |
1702 |
47.26 |
7e-101 |
Dicer-like protein 4 OS Arabidopsis thaliana GN DCL4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|A7LFZ6|DCL4_ORYSJ
|
1 |
362 |
+ |
362 |
Gaps:9 |
22.15 |
1657 |
43.87 |
3e-86 |
Endoribonuclease Dicer homolog 4 OS Oryza sativa subsp. japonica GN DCL4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5N870|DCL3A_ORYSJ
|
15 |
364 |
+ |
350 |
Gaps:34 |
22.53 |
1651 |
26.88 |
4e-23 |
Endoribonuclease Dicer homolog 3a OS Oryza sativa subsp. japonica GN DCL3A PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7XD96|DCL3B_ORYSJ
|
10 |
357 |
+ |
348 |
Gaps:41 |
23.15 |
1637 |
24.01 |
9e-18 |
Endoribonuclease Dicer homolog 3b OS Oryza sativa subsp. japonica GN DCL3B PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9LXW7|DCL3_ARATH
|
105 |
354 |
+ |
250 |
Gaps:42 |
18.10 |
1580 |
24.13 |
1e-11 |
Endoribonuclease Dicer homolog 3 OS Arabidopsis thaliana GN DCL3 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q10HL3|DCL2A_ORYSJ
|
11 |
366 |
+ |
356 |
Gaps:55 |
24.47 |
1410 |
26.96 |
2e-10 |
Endoribonuclease Dicer homolog 2a OS Oryza sativa subsp. japonica GN DCL2A PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q3EBC8|DCL2_ARATH
|
13 |
372 |
+ |
360 |
Gaps:44 |
25.36 |
1388 |
26.14 |
7e-10 |
Endoribonuclease Dicer homolog 2 OS Arabidopsis thaliana GN At3g03300 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q69LX2|DCL2B_ORYSJ
|
21 |
366 |
+ |
346 |
Gaps:52 |
24.55 |
1377 |
26.63 |
1e-09 |
Endoribonuclease Dicer homolog 2b OS Oryza sativa subsp. japonica GN DCL2B PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q8LMR2|DCL1_ORYSJ
|
2 |
267 |
+ |
266 |
Gaps:32 |
14.45 |
1883 |
23.16 |
9e-07 |
Endoribonuclease Dicer homolog 1 OS Oryza sativa subsp. japonica GN DCL1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9SP32|DCL1_ARATH
|
27 |
267 |
+ |
241 |
Gaps:36 |
12.94 |
1909 |
25.10 |
2e-06 |
Endoribonuclease Dicer homolog 1 OS Arabidopsis thaliana GN DCL1 PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|190615
|
2 |
78 |
+ |
77 |
Gaps:2 |
82.42 |
91 |
37.33 |
2e-10 |
pfam03368 dsRNA_bind Double stranded RNA binding domain. This domain is a divergent double stranded RNA-binding domain. It is found in members of the Dicer protein family which function in RNA interference an evolutionarily conserved mechanism for gene silencing using double-stranded RNA (dsRNA) molecules.
|
rpsblast_cdd |
gnl|CDD|30329
|
274 |
360 |
+ |
87 |
Gaps:15 |
72.59 |
135 |
32.65 |
4e-10 |
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_kog |
gnl|CDD|35920
|
1 |
336 |
+ |
336 |
Gaps:10 |
20.30 |
1606 |
11.96 |
1e-14 |
KOG0701 KOG0701 KOG0701 dsRNA-specific nuclease Dicer and related ribonucleases [RNA processing and modification].
|