blastp_kegg |
lcl|csv:101226932
|
3 |
231 |
+ |
229 |
Gaps:39 |
45.91 |
501 |
75.22 |
2e-104 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_kegg |
lcl|cmo:103484088
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.17 |
738 |
75.65 |
8e-103 |
cleavage and polyadenylation specificity factor subunit 2
|
blastp_kegg |
lcl|csv:101215673
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.17 |
738 |
75.65 |
8e-103 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_kegg |
lcl|cam:101489524
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.08 |
740 |
74.78 |
2e-100 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_kegg |
lcl|gmx:100777002
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.12 |
739 |
74.78 |
4e-100 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_kegg |
lcl|pvu:PHAVU_004G114000g
|
1 |
231 |
+ |
231 |
Gaps:39 |
31.39 |
739 |
73.71 |
8e-100 |
hypothetical protein
|
blastp_kegg |
lcl|gmx:100796817
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.17 |
738 |
73.91 |
5e-99 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_kegg |
lcl|pmum:103333205
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.08 |
740 |
73.48 |
2e-98 |
cleavage and polyadenylation specificity factor subunit 2
|
blastp_kegg |
lcl|pper:PRUPE_ppa001928mg
|
3 |
231 |
+ |
229 |
Gaps:39 |
31.08 |
740 |
73.48 |
2e-98 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100267865
|
1 |
231 |
+ |
231 |
Gaps:39 |
31.35 |
740 |
73.71 |
6e-96 |
cleavage and polyadenylation specificity factor subunit 2-like
|
blastp_pdb |
2i7x_A
|
1 |
170 |
+ |
170 |
Gaps:42 |
27.06 |
717 |
27.84 |
9e-13 |
mol:protein length:717 Protein CFT2
|
blastp_pdb |
2i7v_A
|
7 |
217 |
+ |
211 |
Gaps:45 |
45.32 |
459 |
26.92 |
1e-11 |
mol:protein length:459 Cleavage and polyadenylation specificity fact
|
blastp_pdb |
2i7t_A
|
7 |
217 |
+ |
211 |
Gaps:45 |
45.32 |
459 |
26.92 |
1e-11 |
mol:protein length:459 Cleavage and polyadenylation specificity fact
|
blastp_uniprot_sprot |
sp|Q9LKF9|CPSF2_ARATH
|
3 |
228 |
+ |
226 |
Gaps:38 |
30.85 |
739 |
65.79 |
6e-86 |
Cleavage and polyadenylation specificity factor subunit 2 OS Arabidopsis thaliana GN CPSF100 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q652P4|CPSF2_ORYSJ
|
4 |
231 |
+ |
228 |
Gaps:39 |
31.03 |
738 |
65.07 |
2e-81 |
Cleavage and polyadenylation specificity factor subunit 2 OS Oryza sativa subsp. japonica GN Os09g0569400 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9V3D6|CPSF2_DROME
|
4 |
219 |
+ |
216 |
Gaps:40 |
29.10 |
756 |
42.27 |
4e-43 |
Probable cleavage and polyadenylation specificity factor subunit 2 OS Drosophila melanogaster GN Cpsf100 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O35218|CPSF2_MOUSE
|
3 |
219 |
+ |
217 |
Gaps:41 |
28.13 |
782 |
40.91 |
5e-41 |
Cleavage and polyadenylation specificity factor subunit 2 OS Mus musculus GN Cpsf2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q10568|CPSF2_BOVIN
|
3 |
219 |
+ |
217 |
Gaps:41 |
28.13 |
782 |
40.91 |
6e-41 |
Cleavage and polyadenylation specificity factor subunit 2 OS Bos taurus GN CPSF2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9P2I0|CPSF2_HUMAN
|
3 |
219 |
+ |
217 |
Gaps:41 |
28.13 |
782 |
40.91 |
6e-41 |
Cleavage and polyadenylation specificity factor subunit 2 OS Homo sapiens GN CPSF2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9W799|CPSF2_XENLA
|
3 |
219 |
+ |
217 |
Gaps:41 |
28.10 |
783 |
40.91 |
2e-40 |
Cleavage and polyadenylation specificity factor subunit 2 OS Xenopus laevis GN cpsf2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q55BS1|CPSF2_DICDI
|
3 |
219 |
+ |
217 |
Gaps:41 |
28.32 |
784 |
37.84 |
2e-35 |
Cleavage and polyadenylation specificity factor subunit 2 OS Dictyostelium discoideum GN cpsf2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O74740|CFT2_SCHPO
|
1 |
221 |
+ |
221 |
Gaps:49 |
28.86 |
797 |
37.83 |
5e-35 |
Cleavage factor two protein 2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN cft2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O17403|CPSF2_CAEEL
|
15 |
219 |
+ |
205 |
Gaps:42 |
24.79 |
843 |
35.89 |
3e-27 |
Probable cleavage and polyadenylation specificity factor subunit 2 OS Caenorhabditis elegans GN cpsf-2 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|31429
|
6 |
221 |
+ |
216 |
Gaps:45 |
48.01 |
427 |
27.80 |
1e-16 |
COG1236 YSH1 Predicted exonuclease of the beta-lactamase fold involved in RNA processing [Translation ribosomal structure and biogenesis].
|
rpsblast_cdd |
gnl|CDD|198095
|
105 |
219 |
+ |
115 |
Gaps:17 |
77.78 |
126 |
35.71 |
7e-14 |
smart01027 Beta-Casp Beta-Casp domain. The beta-CASP domain is found C terminal to the beta-lactamase domain in pre-mRNA 3'-end-processing endonuclease. The active site of this enzyme is located at the interface of these two domains.
|
rpsblast_cdd |
gnl|CDD|204576
|
105 |
219 |
+ |
115 |
Gaps:23 |
77.42 |
124 |
35.42 |
1e-10 |
pfam10996 Beta-Casp Beta-Casp domain. The beta-CASP domain is found C terminal to the beta-lactamase domain in pre-mRNA 3'-end-processing endonuclease. The active site of this enzyme is located at the interface of these two domains.
|
rpsblast_kog |
gnl|CDD|36350
|
1 |
220 |
+ |
220 |
Gaps:41 |
29.19 |
764 |
48.88 |
2e-64 |
KOG1135 KOG1135 KOG1135 mRNA cleavage and polyadenylation factor II complex subunit CFT2 (CPSF subunit) [RNA processing and modification].
|
rpsblast_kog |
gnl|CDD|36351
|
6 |
215 |
+ |
210 |
Gaps:48 |
40.72 |
501 |
27.94 |
8e-14 |
KOG1136 KOG1136 KOG1136 Predicted cleavage and polyadenylation specificity factor (CPSF subunit) [RNA processing and modification].
|
rpsblast_kog |
gnl|CDD|36352
|
5 |
219 |
+ |
215 |
Gaps:47 |
31.74 |
668 |
28.77 |
3e-13 |
KOG1137 KOG1137 KOG1137 mRNA cleavage and polyadenylation factor II complex BRR5 (CPSF subunit) [RNA processing and modification].
|