blastp_kegg |
lcl|fve:101292189
|
33 |
474 |
+ |
442 |
Gaps:47 |
86.13 |
512 |
30.84 |
5e-39 |
putative F-box/FBD/LRR-repeat protein At1g78760-like
|
blastp_kegg |
lcl|tcc:TCM_031423
|
36 |
475 |
+ |
440 |
Gaps:54 |
94.43 |
449 |
34.43 |
1e-38 |
F-box/RNI/FBD-like domains-containing protein putative
|
blastp_kegg |
lcl|pxb:103926900
|
24 |
474 |
+ |
451 |
Gaps:62 |
99.78 |
456 |
31.43 |
5e-37 |
F-box/LRR-repeat protein At4g14103-like
|
blastp_kegg |
lcl|pxb:103960072
|
36 |
474 |
+ |
439 |
Gaps:51 |
96.58 |
439 |
33.25 |
1e-35 |
FBD-associated F-box protein At4g10400-like
|
blastp_kegg |
lcl|mdm:103432206
|
36 |
474 |
+ |
439 |
Gaps:55 |
96.58 |
439 |
33.49 |
2e-35 |
FBD-associated F-box protein At4g10400-like
|
blastp_kegg |
lcl|fve:101307404
|
35 |
473 |
+ |
439 |
Gaps:47 |
97.09 |
447 |
31.80 |
3e-35 |
putative F-box/FBD/LRR-repeat protein At1g78760-like
|
blastp_kegg |
lcl|pxb:103934882
|
36 |
449 |
+ |
414 |
Gaps:55 |
96.90 |
451 |
30.21 |
2e-34 |
FBD-associated F-box protein At5g60610-like
|
blastp_kegg |
lcl|mdm:103426418
|
35 |
474 |
+ |
440 |
Gaps:75 |
97.89 |
475 |
30.11 |
1e-33 |
F-box/FBD/LRR-repeat protein At4g00160-like
|
blastp_kegg |
lcl|brp:103856930
|
36 |
474 |
+ |
439 |
Gaps:48 |
99.51 |
411 |
34.23 |
2e-33 |
FBD-associated F-box protein At5g56370
|
blastp_kegg |
lcl|pxb:103931550
|
35 |
474 |
+ |
440 |
Gaps:83 |
97.89 |
475 |
30.11 |
4e-33 |
F-box/LRR-repeat protein At3g58900-like
|
blastp_pdb |
4a01_B
|
531 |
622 |
+ |
92 |
Gaps:34 |
18.15 |
766 |
51.80 |
1e-09 |
mol:protein length:766 PROTON PYROPHOSPHATASE
|
blastp_pdb |
4a01_A
|
531 |
622 |
+ |
92 |
Gaps:34 |
18.15 |
766 |
51.80 |
1e-09 |
mol:protein length:766 PROTON PYROPHOSPHATASE
|
blastp_uniprot_sprot |
sp|Q9FM94|FBD21_ARATH
|
36 |
474 |
+ |
439 |
Gaps:60 |
99.52 |
421 |
32.94 |
2e-30 |
FBD-associated F-box protein At5g56370 OS Arabidopsis thaliana GN At5g56370 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SCQ5|FBD10_ARATH
|
36 |
475 |
+ |
440 |
Gaps:46 |
99.77 |
427 |
33.33 |
1e-29 |
Putative FBD-associated F-box protein At3g50710 OS Arabidopsis thaliana GN At3g50710 PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q8L7H1|FBL75_ARATH
|
24 |
379 |
+ |
356 |
Gaps:39 |
92.65 |
381 |
30.31 |
5e-26 |
F-box/LRR-repeat protein At4g14103 OS Arabidopsis thaliana GN At4g14103 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q94B46|FBL74_ARATH
|
24 |
379 |
+ |
356 |
Gaps:56 |
73.93 |
468 |
32.08 |
2e-25 |
F-box/LRR-repeat protein At4g14096 OS Arabidopsis thaliana GN At4g14096 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FF58|FBD30_ARATH
|
36 |
442 |
+ |
407 |
Gaps:62 |
99.23 |
388 |
33.51 |
2e-25 |
FBD-associated F-box protein At5g60610 OS Arabidopsis thaliana GN At5g60610 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LXJ7|FBD11_ARATH
|
28 |
475 |
+ |
448 |
Gaps:69 |
99.28 |
416 |
32.20 |
9e-25 |
FBD-associated F-box protein At3g52670 OS Arabidopsis thaliana GN At3g52670 PE 4 SV 2
|
blastp_uniprot_sprot |
sp|Q9FJU2|FBD37_ARATH
|
38 |
443 |
+ |
406 |
Gaps:60 |
96.98 |
398 |
30.57 |
2e-24 |
Putative FBD-associated F-box protein At5g56700 OS Arabidopsis thaliana GN At5g56700 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q8H1R7|FDL27_ARATH
|
36 |
475 |
+ |
440 |
Gaps:40 |
99.76 |
419 |
29.43 |
4e-24 |
F-box/FBD/LRR-repeat protein At4g26340 OS Arabidopsis thaliana GN At4g26340 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FJT1|FBD29_ARATH
|
35 |
472 |
+ |
438 |
Gaps:72 |
94.25 |
435 |
30.98 |
5e-24 |
Putative FBD-associated F-box protein At5g56820 OS Arabidopsis thaliana GN At5g56820 PE 4 SV 2
|
blastp_uniprot_sprot |
sp|Q9C7M1|FBD2_ARATH
|
35 |
474 |
+ |
440 |
Gaps:44 |
98.10 |
422 |
28.50 |
8e-24 |
Putative FBD-associated F-box protein At1g55030 OS Arabidopsis thaliana GN At1g55030 PE 4 SV 1
|
rpsblast_cdd |
gnl|CDD|177897
|
531 |
622 |
+ |
92 |
Gaps:34 |
18.17 |
765 |
52.52 |
2e-14 |
PLN02255 PLN02255 H(+) -translocating inorganic pyrophosphatase.
|
rpsblast_cdd |
gnl|CDD|130174
|
555 |
622 |
+ |
68 |
Gaps:7 |
8.75 |
697 |
50.82 |
8e-11 |
TIGR01104 V_PPase vacuolar-type H(+)-translocating pyrophosphatase. This model describes proton pyrophosphatases from eukaryotes (predominantly plants) archaea and bacteria. It is an integral membrane protein and is suggested to have about 15 membrane spanning domains. Proton translocating inorganic pyrophosphatase like H(+)-ATPase acidifies the vacuoles and is pivotal to the vacuolar secondary active transport systems in plants.
|
rpsblast_cdd |
gnl|CDD|202513
|
585 |
622 |
+ |
38 |
Gaps:3 |
6.13 |
669 |
51.22 |
3e-09 |
pfam03030 H_PPase Inorganic H+ pyrophosphatase. The H+ pyrophosphatase is an transmembrane proton pump involved in establishing the H+ electrochemical potential difference between the vacuole lumen and the cell cytosol. Vacuolar-type H(+)-translocating inorganic pyrophosphatases have long been considered to be restricted to plants and to a few species of photo-trophic bacteria. However in recent investigations these pyrophosphatases have been found in organisms as disparate as thermophilic Archaea and parasitic protists.
|
rpsblast_cdd |
gnl|CDD|179102
|
585 |
622 |
+ |
38 |
Gaps:3 |
6.16 |
666 |
48.78 |
2e-08 |
PRK00733 hppA membrane-bound proton-translocating pyrophosphatase Validated.
|