blastp_kegg |
lcl|pper:PRUPE_ppa003548mg
|
2 |
567 |
+ |
566 |
Gaps:13 |
99.47 |
566 |
89.88 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103932678
|
2 |
567 |
+ |
566 |
Gaps:13 |
99.47 |
566 |
88.63 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|vvi:100260733
|
2 |
569 |
+ |
568 |
Gaps:5 |
100.00 |
567 |
88.36 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|pxb:103944200
|
2 |
569 |
+ |
568 |
Gaps:13 |
99.82 |
566 |
87.61 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|cit:102623381
|
5 |
569 |
+ |
565 |
Gaps:6 |
99.65 |
573 |
84.59 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|mdm:103446398
|
2 |
567 |
+ |
566 |
Gaps:13 |
100.00 |
563 |
87.74 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|cic:CICLE_v10017475mg
|
5 |
569 |
+ |
565 |
Gaps:6 |
99.65 |
573 |
84.59 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103434805
|
2 |
567 |
+ |
566 |
Gaps:13 |
99.47 |
566 |
88.63 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|csv:101225924
|
2 |
569 |
+ |
568 |
Gaps:14 |
100.00 |
566 |
87.10 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_kegg |
lcl|csv:101208923
|
2 |
569 |
+ |
568 |
Gaps:14 |
100.00 |
566 |
87.10 |
0.0 |
eukaryotic translation initiation factor 3 subunit D-like
|
blastp_uniprot_sprot |
sp|P56820|EIF3D_ARATH
|
8 |
565 |
+ |
558 |
Gaps:25 |
98.31 |
591 |
77.28 |
0.0 |
Eukaryotic translation initiation factor 3 subunit D OS Arabidopsis thaliana GN TIF3D1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6TH15|EIF3D_DANRE
|
16 |
526 |
+ |
511 |
Gaps:38 |
94.02 |
552 |
46.05 |
2e-147 |
Eukaryotic translation initiation factor 3 subunit D OS Danio rerio GN eif3d PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B4HHG8|EI3D2_DROSE
|
13 |
559 |
+ |
547 |
Gaps:53 |
97.82 |
550 |
46.10 |
4e-147 |
Eukaryotic translation initiation factor 3 subunit D-2 OS Drosophila sechellia GN eIF3-S7-2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6P8G0|EIF3D_XENTR
|
6 |
526 |
+ |
521 |
Gaps:44 |
95.83 |
552 |
45.75 |
2e-146 |
Eukaryotic translation initiation factor 3 subunit D OS Xenopus tropicalis GN eif3d PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B4K892|EI3D1_DROMO
|
8 |
526 |
+ |
519 |
Gaps:54 |
92.54 |
563 |
46.64 |
3e-146 |
Eukaryotic translation initiation factor 3 subunit D-1 OS Drosophila mojavensis GN eIF-3p66 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B4QT07|EI3D2_DROSI
|
13 |
526 |
+ |
514 |
Gaps:38 |
94.37 |
551 |
46.15 |
8e-146 |
Eukaryotic translation initiation factor 3 subunit D-2 OS Drosophila simulans GN eIF3-S7-2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O15371|EIF3D_HUMAN
|
16 |
526 |
+ |
511 |
Gaps:41 |
94.16 |
548 |
46.90 |
1e-145 |
Eukaryotic translation initiation factor 3 subunit D OS Homo sapiens GN EIF3D PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q3T122|EIF3D_BOVIN
|
16 |
526 |
+ |
511 |
Gaps:35 |
94.16 |
548 |
45.93 |
1e-145 |
Eukaryotic translation initiation factor 3 subunit D OS Bos taurus GN EIF3D PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6AYK8|EIF3D_RAT
|
16 |
526 |
+ |
511 |
Gaps:35 |
94.16 |
548 |
45.93 |
2e-145 |
Eukaryotic translation initiation factor 3 subunit D OS Rattus norvegicus GN Eif3d PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O70194|EIF3D_MOUSE
|
16 |
526 |
+ |
511 |
Gaps:35 |
94.16 |
548 |
45.93 |
2e-145 |
Eukaryotic translation initiation factor 3 subunit D OS Mus musculus GN Eif3d PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|203164
|
8 |
521 |
+ |
514 |
Gaps:33 |
99.61 |
517 |
53.01 |
0.0 |
pfam05091 eIF-3_zeta Eukaryotic translation initiation factor 3 subunit 7 (eIF-3). This family is made up of eukaryotic translation initiation factor 3 subunit 7 (eIF-3 zeta/eIF3 p66/eIF3d). Eukaryotic initiation factor 3 is a multi-subunit complex that is required for binding of mRNA to 40 S ribosomal subunits stabilisation of ternary complex binding to 40 S subunits and dissociation of 40 and 60 S subunits. These functions and the complex nature of eIF3 suggest multiple interactions with many components of the translational machinery. The gene coding for the protein has been implicated in cancer in mammals.
|
rpsblast_kog |
gnl|CDD|37690
|
8 |
550 |
+ |
543 |
Gaps:25 |
99.09 |
549 |
58.27 |
0.0 |
KOG2479 KOG2479 KOG2479 Translation initiation factor 3 subunit d (eIF-3d) [Translation ribosomal structure and biogenesis].
|