blastp_kegg |
lcl|fve:101292189
|
33 |
453 |
+ |
421 |
Gaps:68 |
86.13 |
512 |
31.97 |
1e-37 |
putative F-box/FBD/LRR-repeat protein At1g78760-like
|
blastp_kegg |
lcl|tcc:TCM_031423
|
36 |
454 |
+ |
419 |
Gaps:49 |
94.43 |
449 |
32.78 |
3e-34 |
F-box/RNI/FBD-like domains-containing protein putative
|
blastp_kegg |
lcl|fve:101307404
|
35 |
452 |
+ |
418 |
Gaps:66 |
97.09 |
447 |
31.80 |
3e-32 |
putative F-box/FBD/LRR-repeat protein At1g78760-like
|
blastp_kegg |
lcl|pxb:103960072
|
36 |
453 |
+ |
418 |
Gaps:66 |
96.58 |
439 |
32.78 |
4e-32 |
FBD-associated F-box protein At4g10400-like
|
blastp_kegg |
lcl|mdm:103432206
|
36 |
453 |
+ |
418 |
Gaps:70 |
96.58 |
439 |
33.02 |
7e-32 |
FBD-associated F-box protein At4g10400-like
|
blastp_kegg |
lcl|pxb:103926900
|
24 |
453 |
+ |
430 |
Gaps:79 |
99.78 |
456 |
30.99 |
2e-31 |
F-box/LRR-repeat protein At4g14103-like
|
blastp_kegg |
lcl|brp:103856930
|
36 |
453 |
+ |
418 |
Gaps:67 |
99.51 |
411 |
33.74 |
8e-31 |
FBD-associated F-box protein At5g56370
|
blastp_kegg |
lcl|mdm:103448871
|
26 |
455 |
+ |
430 |
Gaps:51 |
99.56 |
455 |
29.80 |
2e-30 |
F-box/FBD/LRR-repeat protein At5g56420-like
|
blastp_kegg |
lcl|eus:EUTSA_v10027789mg
|
38 |
454 |
+ |
417 |
Gaps:57 |
98.99 |
398 |
34.77 |
1e-29 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103448794
|
36 |
449 |
+ |
414 |
Gaps:69 |
97.69 |
433 |
32.39 |
1e-29 |
F-box/LRR-repeat protein At4g14103-like
|
blastp_pdb |
4a01_B
|
510 |
582 |
+ |
73 |
Gaps:27 |
12.27 |
766 |
51.06 |
7e-17 |
mol:protein length:766 PROTON PYROPHOSPHATASE
|
blastp_pdb |
4a01_A
|
510 |
582 |
+ |
73 |
Gaps:27 |
12.27 |
766 |
51.06 |
7e-17 |
mol:protein length:766 PROTON PYROPHOSPHATASE
|
blastp_uniprot_sprot |
sp|Q9FM94|FBD21_ARATH
|
36 |
453 |
+ |
418 |
Gaps:65 |
99.52 |
421 |
32.46 |
3e-28 |
FBD-associated F-box protein At5g56370 OS Arabidopsis thaliana GN At5g56370 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SCQ5|FBD10_ARATH
|
36 |
454 |
+ |
419 |
Gaps:69 |
99.77 |
427 |
34.27 |
2e-27 |
Putative FBD-associated F-box protein At3g50710 OS Arabidopsis thaliana GN At3g50710 PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q9SV82|FBD40_ARATH
|
36 |
453 |
+ |
418 |
Gaps:87 |
99.51 |
409 |
31.20 |
3e-24 |
FBD-associated F-box protein At4g10400 OS Arabidopsis thaliana GN At4g10400 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9C7M1|FBD2_ARATH
|
35 |
453 |
+ |
419 |
Gaps:47 |
98.10 |
422 |
28.26 |
1e-23 |
Putative FBD-associated F-box protein At1g55030 OS Arabidopsis thaliana GN At1g55030 PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q9LXJ6|FDL21_ARATH
|
36 |
453 |
+ |
418 |
Gaps:56 |
92.98 |
456 |
31.84 |
1e-23 |
F-box/FBD/LRR-repeat protein At3g52680 OS Arabidopsis thaliana GN At3g52680 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9FJT1|FBD29_ARATH
|
35 |
451 |
+ |
417 |
Gaps:91 |
94.25 |
435 |
30.73 |
1e-23 |
Putative FBD-associated F-box protein At5g56820 OS Arabidopsis thaliana GN At5g56820 PE 4 SV 2
|
blastp_uniprot_sprot |
sp|Q9FF58|FBD30_ARATH
|
36 |
421 |
+ |
386 |
Gaps:71 |
99.23 |
388 |
33.51 |
1e-23 |
FBD-associated F-box protein At5g60610 OS Arabidopsis thaliana GN At5g60610 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FJU2|FBD37_ARATH
|
38 |
422 |
+ |
385 |
Gaps:59 |
96.98 |
398 |
30.31 |
8e-23 |
Putative FBD-associated F-box protein At5g56700 OS Arabidopsis thaliana GN At5g56700 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q3EAE5|FDL24_ARATH
|
36 |
453 |
+ |
418 |
Gaps:85 |
99.55 |
441 |
29.61 |
2e-22 |
Putative F-box/FBD/LRR-repeat protein At4g00315 OS Arabidopsis thaliana GN At4g00315 PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q9FM89|FDL38_ARATH
|
36 |
454 |
+ |
419 |
Gaps:54 |
98.82 |
422 |
30.46 |
3e-22 |
F-box/FBD/LRR-repeat protein At5g56420 OS Arabidopsis thaliana GN At5g56420 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|177897
|
510 |
625 |
+ |
116 |
Gaps:27 |
16.86 |
765 |
57.36 |
1e-22 |
PLN02255 PLN02255 H(+) -translocating inorganic pyrophosphatase.
|
rpsblast_cdd |
gnl|CDD|202513
|
493 |
625 |
+ |
133 |
Gaps:76 |
30.34 |
669 |
25.12 |
5e-16 |
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|130174
|
503 |
625 |
+ |
123 |
Gaps:58 |
23.24 |
697 |
49.38 |
1e-14 |
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|179102
|
499 |
625 |
+ |
127 |
Gaps:79 |
29.73 |
666 |
22.73 |
4e-11 |
PRK00733 hppA membrane-bound proton-translocating pyrophosphatase Validated.
|