blastp_kegg |
lcl|pper:PRUPE_ppa000879mg
|
123 |
374 |
+ |
252 |
Gaps:26 |
27.57 |
972 |
63.43 |
5e-97 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103332192
|
123 |
374 |
+ |
252 |
Gaps:26 |
27.57 |
972 |
63.43 |
7e-97 |
exportin-2
|
blastp_kegg |
lcl|pop:POPTR_0014s09550g
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.56 |
969 |
67.65 |
3e-96 |
POPTRDRAFT_664131 Importin-alpha re-exporter family protein
|
blastp_kegg |
lcl|rcu:RCOM_0716980
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.56 |
969 |
66.39 |
6e-96 |
importin-alpha re-exporter putative
|
blastp_kegg |
lcl|brp:103866460
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.51 |
971 |
65.97 |
7e-96 |
exportin-2
|
blastp_kegg |
lcl|eus:EUTSA_v10001293mg
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.49 |
972 |
65.13 |
8e-96 |
hypothetical protein
|
blastp_kegg |
lcl|cic:CICLE_v10018709mg
|
121 |
374 |
+ |
254 |
Gaps:26 |
27.69 |
975 |
63.33 |
2e-95 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103417637
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.51 |
971 |
66.81 |
4e-95 |
exportin-2-like
|
blastp_kegg |
lcl|pop:POPTR_0002s17340g
|
158 |
374 |
+ |
217 |
Gaps:21 |
24.56 |
969 |
68.07 |
5e-95 |
POPTRDRAFT_644596 Importin-alpha re-exporter family protein
|
blastp_kegg |
lcl|cit:102626753
|
121 |
374 |
+ |
254 |
Gaps:26 |
27.69 |
975 |
62.96 |
9e-95 |
exportin-2-like
|
blastp_pdb |
1wa5_C
|
158 |
373 |
+ |
216 |
Gaps:30 |
25.62 |
960 |
30.08 |
3e-25 |
mol:protein length:960 IMPORTIN ALPHA RE-EXPORTER
|
blastp_pdb |
1z3h_B
|
158 |
373 |
+ |
216 |
Gaps:30 |
25.41 |
968 |
30.08 |
3e-25 |
mol:protein length:968 Importin alpha re-exporter
|
blastp_pdb |
1z3h_A
|
158 |
373 |
+ |
216 |
Gaps:30 |
25.41 |
968 |
30.08 |
3e-25 |
mol:protein length:968 Importin alpha re-exporter
|
blastp_uniprot_sprot |
sp|Q9ZPY7|XPO2_ARATH
|
125 |
374 |
+ |
250 |
Gaps:27 |
27.47 |
972 |
60.67 |
5e-93 |
Exportin-2 OS Arabidopsis thaliana GN CAS PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9ERK4|XPO2_MOUSE
|
162 |
373 |
+ |
212 |
Gaps:24 |
24.30 |
971 |
37.29 |
7e-40 |
Exportin-2 OS Mus musculus GN Cse1l PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5R9J2|XPO2_PONAB
|
162 |
373 |
+ |
212 |
Gaps:24 |
24.30 |
971 |
37.29 |
2e-39 |
Exportin-2 OS Pongo abelii GN CSE1L PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A5D785|XPO2_BOVIN
|
162 |
373 |
+ |
212 |
Gaps:24 |
24.30 |
971 |
37.29 |
2e-39 |
Exportin-2 OS Bos taurus GN CSE1L PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P55060|XPO2_HUMAN
|
162 |
373 |
+ |
212 |
Gaps:24 |
24.30 |
971 |
37.29 |
3e-39 |
Exportin-2 OS Homo sapiens GN CSE1L PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q8AY73|XPO2_ORENI
|
163 |
373 |
+ |
211 |
Gaps:24 |
24.20 |
971 |
37.02 |
3e-39 |
Exportin-2 OS Oreochromis niloticus GN cse1l PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9XZU1|XPO2_DROME
|
163 |
400 |
+ |
238 |
Gaps:35 |
28.00 |
975 |
34.43 |
3e-38 |
Exportin-2 OS Drosophila melanogaster GN Cas PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9PTU3|XPO2_PAGMA
|
163 |
373 |
+ |
211 |
Gaps:24 |
24.20 |
971 |
35.74 |
8e-38 |
Exportin-2 OS Pagrus major GN cse1l PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6GMY9|XPO2_XENLA
|
162 |
367 |
+ |
206 |
Gaps:24 |
23.69 |
971 |
36.52 |
6e-37 |
Exportin-2 OS Xenopus laevis GN cse1l PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7SZC2|XPO2_DANRE
|
162 |
367 |
+ |
206 |
Gaps:24 |
23.69 |
971 |
36.52 |
1e-35 |
Exportin-2 OS Danio rerio GN cse1l PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|117083
|
161 |
315 |
+ |
155 |
Gaps:23 |
48.11 |
370 |
44.38 |
3e-50 |
pfam08506 Cse1 Cse1. This domain is present in Cse1 nuclear export receptor proteins. Cse1 mediates the nuclear export of importin alpha. This domain contains HEAT repeats.
|
rpsblast_cdd |
gnl|CDD|190619
|
316 |
371 |
+ |
56 |
none |
12.87 |
435 |
51.79 |
4e-18 |
pfam03378 CAS_CSE1 CAS/CSE protein C-terminus. Mammalian cellular apoptosis susceptibility (CAS) proteins are homologous to the yeast chromosome-segregation protein CSE1. This family aligns the C-terminal halves (approximately). CAS is involved in both cellular apoptosis and proliferation. Apoptosis is inhibited in CAS-depleted cells while the expression of CAS correlates to the degree of cellular proliferation. Like CSE1 it is essential for the mitotic checkpoint in the cell cycle (CAS depletion blocks the cell in the G2 phase) and has been shown to be associated with the microtubule network and the mitotic spindle as is the protein MEK which is thought to regulate the intracellular localisation (predominantly nuclear vs. predominantly cytosolic) of CAS. In the nucleus CAS acts as a nuclear transport factor in the importin pathway. The importin pathway mediates the nuclear transport of several proteins that are necessary for mitosis and further progression. CAS is therefore thought to affect the cell cycle through its effect on the nuclear transport of these proteins. Since apoptosis also requires the nuclear import of several proteins (such as P53 and transcription factors) it has been suggested that CAS also enables apoptosis by facilitating the nuclear import of at least a subset of these essential proteins.
|
rpsblast_cdd |
gnl|CDD|35216
|
163 |
378 |
+ |
216 |
Gaps:30 |
24.08 |
947 |
18.42 |
2e-07 |
COG5657 CSE1 CAS/CSE protein involved in chromosome segregation [Cell division and chromosome partitioning].
|
rpsblast_kog |
gnl|CDD|37203
|
161 |
378 |
+ |
218 |
Gaps:30 |
25.21 |
960 |
41.74 |
3e-61 |
KOG1992 KOG1992 KOG1992 Nuclear export receptor CSE1/CAS (importin beta superfamily) [Nuclear structure Intracellular trafficking secretion and vesicular transport].
|
rpsblast_kog |
gnl|CDD|39424
|
347 |
508 |
+ |
162 |
Gaps:21 |
43.38 |
325 |
34.75 |
9e-28 |
KOG4223 KOG4223 KOG4223 Reticulocalbin calumenin DNA supercoiling factor and related Ca2+-binding proteins of the CREC family (EF-Hand protein superfamily) [Signal transduction mechanisms Intracellular trafficking secretion and vesicular transport].
|
rpsblast_kog |
gnl|CDD|35267
|
341 |
482 |
+ |
142 |
Gaps:38 |
64.25 |
193 |
33.06 |
2e-09 |
KOG0044 KOG0044 KOG0044 Ca2+ sensor (EF-Hand superfamily) [Signal transduction mechanisms].
|