blastp_kegg |
lcl|vvi:100263418
|
1 |
336 |
+ |
336 |
none |
100.00 |
336 |
82.44 |
0.0 |
uncharacterized LOC100263418
|
blastp_kegg |
lcl|vvi:100259526
|
1 |
336 |
+ |
336 |
Gaps:1 |
98.83 |
341 |
79.82 |
0.0 |
uncharacterized LOC100259526
|
blastp_kegg |
lcl|rcu:RCOM_0798510
|
2 |
336 |
+ |
335 |
Gaps:1 |
98.25 |
342 |
77.68 |
0.0 |
3'-5' exonuclease putative
|
blastp_kegg |
lcl|pper:PRUPE_ppa008192mg
|
2 |
336 |
+ |
335 |
none |
97.95 |
342 |
76.72 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103320522
|
2 |
336 |
+ |
335 |
Gaps:1 |
97.96 |
343 |
76.79 |
0.0 |
exosome component 10
|
blastp_kegg |
lcl|cic:CICLE_v10008867mg
|
1 |
336 |
+ |
336 |
Gaps:5 |
98.81 |
335 |
76.44 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102615602
|
1 |
336 |
+ |
336 |
Gaps:5 |
98.81 |
335 |
76.44 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|csv:101223734
|
1 |
336 |
+ |
336 |
Gaps:1 |
99.12 |
340 |
75.07 |
0.0 |
uncharacterized LOC101223734
|
blastp_kegg |
lcl|csv:101214970
|
1 |
336 |
+ |
336 |
Gaps:1 |
99.12 |
340 |
75.07 |
0.0 |
uncharacterized LOC101214970
|
blastp_kegg |
lcl|pxb:103929643
|
6 |
336 |
+ |
331 |
none |
96.50 |
343 |
76.13 |
0.0 |
uncharacterized LOC103929643
|
blastp_pdb |
3sah_B
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
33.33 |
6e-08 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sah_A
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
33.33 |
6e-08 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sag_B
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
32.59 |
4e-07 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sag_A
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
32.59 |
4e-07 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3saf_B
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
32.59 |
4e-07 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3saf_A
|
70 |
224 |
+ |
155 |
Gaps:20 |
31.54 |
428 |
32.59 |
4e-07 |
mol:protein length:428 Exosome component 10
|
blastp_uniprot_sprot |
sp|Q8CDF7|EXD1_MOUSE
|
52 |
201 |
+ |
150 |
Gaps:10 |
26.67 |
570 |
34.21 |
2e-16 |
Exonuclease 3'-5' domain-containing protein 1 OS Mus musculus GN Exd1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8NHP7|EXD1_HUMAN
|
52 |
201 |
+ |
150 |
Gaps:10 |
29.57 |
514 |
34.87 |
4e-16 |
Exonuclease 3'-5' domain-containing protein 1 OS Homo sapiens GN EXD1 PE 2 SV 4
|
blastp_uniprot_sprot |
sp|Q6NRD5|EXD1_XENLA
|
52 |
221 |
+ |
170 |
Gaps:14 |
38.74 |
444 |
30.23 |
8e-13 |
Exonuclease 3'-5' domain-containing protein 1 OS Xenopus laevis GN exd1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P56960|EXOSX_MOUSE
|
70 |
228 |
+ |
159 |
Gaps:20 |
15.67 |
887 |
31.65 |
4e-07 |
Exosome component 10 OS Mus musculus GN Exosc10 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q01780|EXOSX_HUMAN
|
70 |
224 |
+ |
155 |
Gaps:20 |
15.25 |
885 |
32.59 |
3e-06 |
Exosome component 10 OS Homo sapiens GN EXOSC10 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q0P3U3|EXD1_DANRE
|
72 |
163 |
+ |
92 |
Gaps:1 |
24.60 |
378 |
33.33 |
8e-06 |
Exonuclease 3'-5' domain-containing protein 1 OS Danio rerio GN exd1 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|99851
|
46 |
241 |
+ |
196 |
Gaps:4 |
99.49 |
197 |
43.88 |
2e-62 |
cd06148 Egl_like_exo DEDDy 3'-5' exonuclease domain of Drosophila Egalitarian (Egl) and similar proteins. The Egalitarian (Egl) protein subfamily is composed of Drosophila Egl and similar proteins. Egl is a component of an mRNA-binding complex which is required for oocyte specification. Egl contains a DEDDy-type DnaQ-like 3'-5' exonuclease domain possessing three conserved sequence motifs termed ExoI ExoII and ExoIII with a specific YX(3)D pattern at ExoIII. The motifs are clustered around the active site and contain four conserved acidic residues that serve as ligands for the two metal ions required for catalysis. The conservation of this subfamily throughout eukaryotes suggests that its members may be part of ancient RNA processing complexes that are likely to participate in the regulated processing of specific mRNAs. Some members of this subfamily do not have a completely conserved YX(3)D pattern at the ExoIII motif.
|
rpsblast_cdd |
gnl|CDD|176654
|
56 |
230 |
+ |
175 |
Gaps:21 |
87.64 |
178 |
32.69 |
4e-23 |
cd06142 RNaseD_exo DEDDy 3'-5' exonuclease domain of Ribonuclease D and similar proteins. Ribonuclease (RNase) D is a bacterial enzyme involved in the maturation of small stable RNAs and the 3' maturation of tRNA. It contains a DEDDy-type DnaQ-like 3'-5' exonuclease domain possessing three conserved sequence motifs termed ExoI ExoII and ExoIII with a specific YX(3)D pattern at ExoIII. These motifs are clustered around the active site and contain four conserved acidic residues that serve as ligands for the two metal ions required for catalysis. In vivo RNase D only becomes essential upon removal of other ribonucleases. Eukaryotic RNase D homologs include yeast Rrp6p human PM/Scl-100 and the Drosophila melanogaster egalitarian protein.
|
rpsblast_cdd |
gnl|CDD|28891
|
56 |
221 |
+ |
166 |
Gaps:14 |
99.35 |
155 |
30.52 |
1e-20 |
cd00007 35EXOc 3'-5' exonuclease. The 35EXOc domain is responsible for the 3'-5' exonuclease proofreading activity of prokaryotic DNA polymerase I (pol I) and other enzymes it catalyses the hydrolysis of unpaired or mismatched nucleotides. This domain consists of the amino-terminal half of the Klenow fragment in E. coli pol I. 35EXOc is also found in the Werner syndrome helicase (WRN) focus forming activity 1 protein (FFA-1) and ribonuclease D (RNase D)..
|
rpsblast_cdd |
gnl|CDD|201888
|
33 |
221 |
+ |
189 |
Gaps:24 |
99.42 |
172 |
35.67 |
1e-19 |
pfam01612 DNA_pol_A_exo1 3'-5' exonuclease. This domain is responsible for the 3'-5' exonuclease proofreading activity of E. coli DNA polymerase I (polI) and other enzymes it catalyzes the hydrolysis of unpaired or mismatched nucleotides. This domain consists of the amino-terminal half of the Klenow fragment in E. coli polI it is also found in the Werner syndrome helicase (WRN) focus forming activity 1 protein (FFA-1) and ribonuclease D (RNase D). Werner syndrome is a human genetic disorder causing premature aging the WRN protein has helicase activity in the 3'-5' direction. The FFA-1 protein is required for formation of a replication foci and also has helicase activity it is a homologue of the WRN protein. RNase D is a 3'-5' exonuclease involved in tRNA processing. Also found in this family is the autoantigen PM/Scl thought to be involved in polymyositis-scleroderma overlap syndrome.
|
rpsblast_cdd |
gnl|CDD|197748
|
33 |
221 |
+ |
189 |
Gaps:22 |
99.42 |
172 |
29.82 |
7e-18 |
smart00474 35EXOc 3'-5' exonuclease. 3\' -5' exonuclease proofreading domain present in DNA polymerase I Werner syndrome helicase RNase D and other enzymes.
|
rpsblast_cdd |
gnl|CDD|30697
|
57 |
230 |
+ |
174 |
Gaps:20 |
43.21 |
361 |
28.21 |
4e-14 |
COG0349 Rnd Ribonuclease D [Translation ribosomal structure and biogenesis].
|
rpsblast_cdd |
gnl|CDD|176653
|
52 |
223 |
+ |
172 |
Gaps:41 |
91.18 |
170 |
29.03 |
7e-08 |
cd06141 WRN_exo DEDDy 3'-5' exonuclease domain of WRN and similar proteins. WRN is a unique RecQ DNA helicase exhibiting an exonuclease activity. It contains a DEDDy-type DnaQ-like 3'-5' exonuclease domain possessing three conserved sequence motifs termed ExoI ExoII and ExoIII with a specific YX(3)D pattern at ExoIII. These motifs are clustered around the active site and contain four conserved acidic residues that serve as ligands for the two metal ions required for catalysis. Mutations in the WRN gene cause Werner syndrome an autosomal recessive disorder associated with premature aging and increased susceptibility to cancer and type II diabetes. WRN interacts with key proteins involved in DNA replication recombination and repair. It is believed to maintain genomic stability and life span by participating in DNA processes. WRN is stimulated by Ku70/80 an important regulator of genomic stability.
|
rpsblast_cdd |
gnl|CDD|180237
|
52 |
144 |
+ |
93 |
Gaps:4 |
10.80 |
880 |
27.37 |
6e-07 |
PRK05755 PRK05755 DNA polymerase I Provisional.
|