blastp_kegg |
lcl|pper:PRUPE_ppa001105mg
|
23 |
405 |
+ |
383 |
Gaps:52 |
44.82 |
908 |
64.62 |
1e-170 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103342295
|
35 |
405 |
+ |
371 |
Gaps:52 |
42.98 |
919 |
65.06 |
5e-166 |
uncharacterized LOC103342295
|
blastp_kegg |
lcl|mdm:103430914
|
35 |
399 |
+ |
365 |
Gaps:56 |
45.28 |
868 |
64.38 |
1e-159 |
exosome component 10-like
|
blastp_kegg |
lcl|pxb:103944375
|
35 |
399 |
+ |
365 |
Gaps:56 |
43.00 |
914 |
63.61 |
5e-158 |
exosome component 10
|
blastp_kegg |
lcl|pda:103719935
|
23 |
368 |
+ |
346 |
Gaps:42 |
47.15 |
772 |
64.56 |
2e-157 |
exosome component 10-like
|
blastp_kegg |
lcl|csv:101223669
|
11 |
403 |
+ |
393 |
Gaps:64 |
42.89 |
935 |
64.34 |
2e-157 |
exosome component 10-like
|
blastp_kegg |
lcl|csv:101220390
|
11 |
403 |
+ |
393 |
Gaps:64 |
42.84 |
936 |
64.34 |
2e-157 |
exosome component 10-like
|
blastp_kegg |
lcl|cmo:103485997
|
11 |
403 |
+ |
393 |
Gaps:65 |
42.86 |
938 |
63.93 |
7e-157 |
exosome component 10
|
blastp_kegg |
lcl|mdm:103449428
|
35 |
399 |
+ |
365 |
Gaps:55 |
43.15 |
913 |
63.71 |
5e-153 |
exosome component 10-like
|
blastp_kegg |
lcl|gmx:100819332
|
20 |
368 |
+ |
349 |
Gaps:47 |
41.28 |
877 |
67.96 |
2e-152 |
exosome component 10-like
|
blastp_pdb |
3sah_B
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.50 |
9e-46 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sah_A
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.50 |
9e-46 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sag_B
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.00 |
5e-45 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3sag_A
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.00 |
5e-45 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3saf_B
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.00 |
5e-45 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
3saf_A
|
190 |
403 |
+ |
214 |
Gaps:16 |
46.73 |
428 |
47.00 |
5e-45 |
mol:protein length:428 Exosome component 10
|
blastp_pdb |
2hbm_A
|
240 |
368 |
+ |
129 |
Gaps:5 |
31.22 |
410 |
52.34 |
1e-34 |
mol:protein length:410 Exosome complex exonuclease RRP6
|
blastp_pdb |
2hbl_A
|
240 |
368 |
+ |
129 |
Gaps:5 |
31.22 |
410 |
52.34 |
1e-34 |
mol:protein length:410 Exosome complex exonuclease RRP6
|
blastp_pdb |
2hbk_A
|
240 |
368 |
+ |
129 |
Gaps:5 |
31.22 |
410 |
52.34 |
1e-34 |
mol:protein length:410 Exosome complex exonuclease RRP6
|
blastp_pdb |
2hbj_A
|
240 |
368 |
+ |
129 |
Gaps:5 |
31.22 |
410 |
52.34 |
1e-34 |
mol:protein length:410 Exosome complex exonuclease RRP6
|
blastp_uniprot_sprot |
sp|P56960|EXOSX_MOUSE
|
94 |
403 |
+ |
310 |
Gaps:74 |
37.88 |
887 |
37.20 |
1e-47 |
Exosome component 10 OS Mus musculus GN Exosc10 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q01780|EXOSX_HUMAN
|
94 |
403 |
+ |
310 |
Gaps:74 |
37.97 |
885 |
36.90 |
4e-47 |
Exosome component 10 OS Homo sapiens GN EXOSC10 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q12149|RRP6_YEAST
|
39 |
368 |
+ |
330 |
Gaps:30 |
43.66 |
733 |
32.19 |
2e-36 |
Exosome complex exonuclease RRP6 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN RRP6 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q10146|RRP6_SCHPO
|
140 |
367 |
+ |
228 |
Gaps:23 |
31.79 |
777 |
37.25 |
4e-32 |
Exosome complex exonuclease rrp6 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN rrp6 PE 3 SV 2
|
rpsblast_cdd |
gnl|CDD|99850
|
233 |
398 |
+ |
166 |
Gaps:15 |
78.65 |
192 |
56.95 |
2e-63 |
cd06147 Rrp6p_like_exo DEDDy 3'-5' exonuclease domain of yeast Rrp6p human polymyositis/scleroderma autoantigen 100kDa and similar proteins. Yeast Rrp6p and its human homolog the polymyositis/scleroderma autoantigen 100kDa (PM/Scl-100) are exosome-associated proteins involved in the degradation and processing of precursors to stable RNAs. Both proteins contain 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. PM/Scl-100 an autoantigen present in the nucleolar compartment of the cell reacts with autoantibodies produced by about 50% of patients with polymyositis-scleroderma overlap syndrome.
|
rpsblast_cdd |
gnl|CDD|201888
|
245 |
399 |
+ |
155 |
Gaps:18 |
83.14 |
172 |
34.97 |
3e-28 |
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|176654
|
245 |
392 |
+ |
148 |
Gaps:17 |
74.72 |
178 |
38.35 |
9e-24 |
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|197748
|
237 |
400 |
+ |
164 |
Gaps:20 |
88.37 |
172 |
34.21 |
2e-19 |
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|176650
|
258 |
368 |
+ |
111 |
Gaps:3 |
69.57 |
161 |
32.14 |
4e-18 |
cd06129 RNaseD_like DEDDy 3'-5' exonuclease domain of RNase D WRN and similar proteins. The RNase D-like group is composed of RNase D WRN and similar proteins. They contain a DEDDy-type DnaQ-like 3'-5' exonuclease domain that contains 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. RNase D is involved in the 3'-end processing of tRNA precursors. RNase D-like proteins in eukaryotes include yeast Rrp6p human PM/Scl-100 and Drosophila melanogaster egalitarian (Egl) protein. WRN is a unique DNA helicase possessing exonuclease activity. Mutation in the WRN gene is implicated in Werner syndrome a disease associated with premature aging and increased predisposition to cancer. Yeast Rrp6p and the human Polymyositis/scleroderma autoantigen 100kDa (PM/Scl-100) are exosome-associated proteins involved in the degradation and processing of precursors to stable RNAs. Egl is a component of an mRNA-binding complex which is required for oocyte specification. The Egl subfamily does not possess a completely conserved YX(3)D pattern at the ExoIII motif.
|
rpsblast_cdd |
gnl|CDD|30697
|
240 |
367 |
+ |
128 |
Gaps:2 |
35.46 |
361 |
30.47 |
1e-16 |
COG0349 Rnd Ribonuclease D [Translation ribosomal structure and biogenesis].
|