blastp_kegg |
lcl|gmx:100788190
|
7 |
267 |
+ |
261 |
Gaps:7 |
30.88 |
842 |
82.31 |
4e-136 |
potassium transporter 7-like
|
blastp_kegg |
lcl|gmx:100788008
|
7 |
267 |
+ |
261 |
Gaps:6 |
30.80 |
841 |
81.08 |
1e-135 |
potassium transporter 7-like
|
blastp_kegg |
lcl|mdm:103444868
|
1 |
267 |
+ |
267 |
Gaps:8 |
31.45 |
849 |
83.52 |
5e-132 |
potassium transporter 7-like
|
blastp_kegg |
lcl|gmx:100778388
|
4 |
267 |
+ |
264 |
Gaps:9 |
30.58 |
847 |
77.61 |
9e-129 |
potassium transporter 7-like
|
blastp_kegg |
lcl|mtr:MTR_2g008820
|
1 |
267 |
+ |
267 |
Gaps:4 |
29.69 |
906 |
76.21 |
9e-128 |
Potassium transporter
|
blastp_kegg |
lcl|gmx:100803841
|
4 |
267 |
+ |
264 |
Gaps:8 |
30.50 |
846 |
78.68 |
2e-127 |
potassium transporter 7-like
|
blastp_kegg |
lcl|pop:POPTR_0003s01820g
|
12 |
267 |
+ |
256 |
Gaps:4 |
30.41 |
855 |
81.15 |
5e-127 |
POPTRDRAFT_712230 potassium transporter family protein
|
blastp_kegg |
lcl|pxb:103940983
|
1 |
267 |
+ |
267 |
Gaps:5 |
31.85 |
854 |
81.62 |
6e-127 |
potassium transporter 7-like
|
blastp_kegg |
lcl|pxb:103930295
|
1 |
267 |
+ |
267 |
Gaps:4 |
31.77 |
853 |
81.55 |
3e-126 |
potassium transporter 7-like
|
blastp_kegg |
lcl|cam:101496674
|
1 |
267 |
+ |
267 |
Gaps:9 |
29.51 |
881 |
80.77 |
4e-125 |
potassium transporter 7-like
|
blastp_uniprot_sprot |
sp|Q8LPL8|POT13_ARATH
|
4 |
267 |
+ |
264 |
Gaps:4 |
30.41 |
855 |
70.77 |
1e-107 |
Potassium transporter 13 OS Arabidopsis thaliana GN POT13 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FY75|POT7_ARATH
|
3 |
261 |
+ |
259 |
Gaps:11 |
29.84 |
858 |
76.56 |
6e-107 |
Potassium transporter 7 OS Arabidopsis thaliana GN POT7 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q69RI8|HAK14_ORYSJ
|
12 |
268 |
+ |
257 |
Gaps:8 |
30.38 |
859 |
65.52 |
2e-95 |
Probable potassium transporter 14 OS Oryza sativa subsp. japonica GN HAK14 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7XPL3|HAK15_ORYSJ
|
62 |
268 |
+ |
207 |
Gaps:1 |
23.99 |
867 |
69.71 |
1e-76 |
Probable potassium transporter 15 OS Oryza sativa subsp. japonica GN HAK15 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q6H4R6|HAK23_ORYSJ
|
12 |
259 |
+ |
248 |
Gaps:14 |
29.87 |
877 |
51.15 |
2e-72 |
Potassium transporter 23 OS Oryza sativa subsp. japonica GN HAK23 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O80739|POT12_ARATH
|
17 |
259 |
+ |
243 |
Gaps:13 |
27.81 |
827 |
58.26 |
6e-71 |
Putative potassium transporter 12 OS Arabidopsis thaliana GN POT12 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9M7K4|POT5_ARATH
|
41 |
259 |
+ |
219 |
Gaps:18 |
27.64 |
785 |
48.39 |
3e-59 |
Potassium transporter 5 OS Arabidopsis thaliana GN POT5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q5JK32|HAK5_ORYSJ
|
71 |
265 |
+ |
195 |
Gaps:2 |
24.71 |
781 |
48.70 |
1e-55 |
Potassium transporter 5 OS Oryza sativa subsp. japonica GN HAK5 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q6H4M2|HAK19_ORYSJ
|
94 |
259 |
+ |
166 |
Gaps:1 |
22.24 |
742 |
55.15 |
4e-54 |
Potassium transporter 19 OS Oryza sativa subsp. japonica GN HAK19 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6VVA6|HAK1_ORYSJ
|
71 |
259 |
+ |
189 |
Gaps:1 |
23.47 |
801 |
48.94 |
2e-53 |
Potassium transporter 1 OS Oryza sativa subsp. japonica GN HAK1 PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|177754
|
2 |
268 |
+ |
267 |
Gaps:3 |
30.99 |
852 |
72.35 |
1e-135 |
PLN00151 PLN00151 potassium transporter Provisional.
|
rpsblast_cdd |
gnl|CDD|165718
|
101 |
265 |
+ |
165 |
Gaps:4 |
20.67 |
779 |
52.17 |
6e-58 |
PLN00150 PLN00150 potassium ion transporter family protein Provisional.
|
rpsblast_cdd |
gnl|CDD|177752
|
94 |
268 |
+ |
175 |
Gaps:3 |
22.42 |
785 |
49.43 |
7e-49 |
PLN00148 PLN00148 potassium transporter Provisional.
|
rpsblast_cdd |
gnl|CDD|129876
|
101 |
269 |
+ |
169 |
Gaps:2 |
24.27 |
688 |
46.71 |
1e-48 |
TIGR00794 kup potassium uptake protein. Proteins of the KUP family include the KUP (TrkD) protein of E. coli a partially sequenced ORF from Lactococcus lactis high affinity K+ uptake systems (Hak1) of the yeast Debaryomyces occidentalis as well as the fungus Neurospora crassa and several homologues in plants. While the E. coli KUP protein is assumed to be a secondary transporter and uptake is blocked by protonophores such as CCCP (but not arsenate) the energy coupling mechanism has not been defined. However the N. crassa protein has been shown to be a K+:H+ symporter establishing that the KUP family consists of secondary carriers. The plant high affinity (20mM) K+ transporter can complement K+ uptake defects in E. coli.
|
rpsblast_cdd |
gnl|CDD|202355
|
102 |
266 |
+ |
165 |
Gaps:39 |
24.34 |
534 |
53.08 |
2e-45 |
pfam02705 K_trans K+ potassium transporter. This is a family of K+ potassium transporters that are conserved across phyla having both bacterial (KUP) yeast (HAK) and plant (AtKT) sequences as members.
|
rpsblast_cdd |
gnl|CDD|177753
|
99 |
263 |
+ |
165 |
Gaps:9 |
21.82 |
779 |
50.00 |
5e-45 |
PLN00149 PLN00149 potassium transporter Provisional.
|
rpsblast_cdd |
gnl|CDD|32972
|
100 |
260 |
+ |
161 |
Gaps:42 |
19.62 |
627 |
44.72 |
4e-27 |
COG3158 Kup K+ transporter [Inorganic ion transport and metabolism].
|
rpsblast_cdd |
gnl|CDD|182693
|
99 |
260 |
+ |
162 |
Gaps:43 |
19.77 |
622 |
44.72 |
6e-20 |
PRK10745 trkD potassium transport protein Kup Provisional.
|