|
blastp_kegg |
lcl|pper:PRUPE_ppa002030mg
|
5 |
452 |
+ |
448 |
Gaps:17 |
59.37 |
726 |
82.83 |
0.0 |
hypothetical protein
|
|
blastp_kegg |
lcl|pmum:103341187
|
7 |
452 |
+ |
446 |
Gaps:17 |
56.60 |
758 |
82.75 |
0.0 |
protein ENHANCED DISEASE RESISTANCE 2-like
|
|
blastp_kegg |
lcl|mdm:103400336
|
7 |
452 |
+ |
446 |
Gaps:3 |
85.91 |
518 |
78.20 |
0.0 |
protein ENHANCED DISEASE RESISTANCE 2-like
|
|
blastp_kegg |
lcl|gmx:100780025
|
7 |
452 |
+ |
446 |
Gaps:5 |
59.62 |
743 |
78.78 |
0.0 |
uncharacterized LOC100780025
|
|
blastp_kegg |
lcl|gmx:100801191
|
7 |
452 |
+ |
446 |
Gaps:5 |
59.30 |
747 |
79.23 |
0.0 |
uncharacterized LOC100801191
|
|
blastp_kegg |
lcl|mdm:103424788
|
7 |
452 |
+ |
446 |
Gaps:20 |
56.84 |
753 |
82.01 |
0.0 |
protein ENHANCED DISEASE RESISTANCE 2-like
|
|
blastp_kegg |
lcl|pxb:103930781
|
7 |
452 |
+ |
446 |
Gaps:20 |
56.84 |
753 |
81.78 |
0.0 |
protein ENHANCED DISEASE RESISTANCE 2-like
|
|
blastp_kegg |
lcl|pxb:103949124
|
7 |
452 |
+ |
446 |
Gaps:20 |
56.84 |
753 |
81.78 |
0.0 |
protein ENHANCED DISEASE RESISTANCE 2-like
|
|
blastp_kegg |
lcl|vvi:100260203
|
4 |
451 |
+ |
448 |
Gaps:1 |
59.39 |
756 |
75.50 |
0.0 |
uncharacterized LOC100260203
|
|
blastp_kegg |
lcl|cam:101503113
|
7 |
451 |
+ |
445 |
Gaps:4 |
59.54 |
744 |
77.43 |
0.0 |
uncharacterized LOC101503113
|
|
blastp_uniprot_sprot |
sp|O50055|COL1_ARATH
|
380 |
530 |
+ |
151 |
Gaps:22 |
40.85 |
355 |
44.83 |
1e-20 |
Zinc finger protein CONSTANS-LIKE 1 OS Arabidopsis thaliana GN COL1 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q9FHH8|COL5_ARATH
|
445 |
530 |
+ |
86 |
Gaps:9 |
26.76 |
355 |
52.63 |
5e-20 |
Zinc finger protein CONSTANS-LIKE 5 OS Arabidopsis thaliana GN COL5 PE 2 SV 2
|
|
blastp_uniprot_sprot |
sp|Q9FDX8|HD1_ORYSJ
|
442 |
530 |
+ |
89 |
Gaps:10 |
24.05 |
395 |
53.68 |
2e-19 |
Zinc finger protein HD1 OS Oryza sativa subsp. japonica GN HD1 PE 2 SV 1
|
|
blastp_uniprot_sprot |
sp|Q39057|CONS_ARATH
|
383 |
530 |
+ |
148 |
Gaps:27 |
38.87 |
373 |
44.83 |
4e-19 |
Zinc finger protein CONSTANS OS Arabidopsis thaliana GN CO PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q940T9|COL4_ARATH
|
460 |
530 |
+ |
71 |
Gaps:6 |
21.27 |
362 |
58.44 |
9e-19 |
Zinc finger protein CONSTANS-LIKE 4 OS Arabidopsis thaliana GN COL4 PE 2 SV 2
|
|
blastp_uniprot_sprot |
sp|Q9SK53|COL3_ARATH
|
461 |
513 |
+ |
53 |
none |
18.03 |
294 |
79.25 |
7e-18 |
Zinc finger protein CONSTANS-LIKE 3 OS Arabidopsis thaliana GN COL3 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q96502|COL2_ARATH
|
461 |
530 |
+ |
70 |
Gaps:8 |
22.48 |
347 |
60.26 |
7e-17 |
Zinc finger protein CONSTANS-LIKE 2 OS Arabidopsis thaliana GN COL2 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q9C9A9|COL7_ARATH
|
468 |
510 |
+ |
43 |
none |
10.97 |
392 |
69.77 |
2e-09 |
Zinc finger protein CONSTANS-LIKE 7 OS Arabidopsis thaliana GN COL7 PE 2 SV 1
|
|
blastp_uniprot_sprot |
sp|Q9M9B3|COL8_ARATH
|
468 |
510 |
+ |
43 |
none |
13.48 |
319 |
67.44 |
6e-09 |
Zinc finger protein CONSTANS-LIKE 8 OS Arabidopsis thaliana GN COL8 PE 2 SV 2
|
|
blastp_uniprot_sprot |
sp|O22800|COL14_ARATH
|
466 |
513 |
+ |
48 |
none |
11.94 |
402 |
56.25 |
1e-08 |
Zinc finger protein CONSTANS-LIKE 14 OS Arabidopsis thaliana GN COL14 PE 2 SV 2
|
|
rpsblast_cdd |
gnl|CDD|115696
|
237 |
442 |
+ |
206 |
Gaps:8 |
99.53 |
215 |
53.27 |
9e-83 |
pfam07059 DUF1336 Protein of unknown function (DUF1336). This family represents the C-terminus (approximately 250 residues) of a number of hypothetical plant proteins of unknown function.
|
|
rpsblast_cdd |
gnl|CDD|177782
|
4 |
448 |
+ |
445 |
Gaps:25 |
58.97 |
719 |
36.08 |
2e-77 |
PLN00188 PLN00188 enhanced disease resistance protein (EDR2) Provisional.
|
|
rpsblast_cdd |
gnl|CDD|203407
|
469 |
510 |
+ |
42 |
none |
93.33 |
45 |
73.81 |
2e-16 |
pfam06203 CCT CCT motif. This short motif is found in a number of plant proteins. It is rich in basic amino acids and has been called a CCT motif after Co Col and Toc1. The CCT motif is about 45 amino acids long and contains a putative nuclear localisation signal within the second half of the CCT motif. Toc1 mutants have been identified in this region.
|
|
rpsblast_cdd |
gnl|CDD|176851
|
2 |
104 |
+ |
103 |
Gaps:12 |
53.37 |
193 |
28.16 |
6e-15 |
cd00177 START Lipid-binding START domain of mammalian STARD1-STARD15 and related proteins. This family includes the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15 and related domains such as the START domain of the Arabidopsis homeobox protein GLABRA 2. The mammalian STARDs are grouped into 8 subfamilies. This family belongs to the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket. For some members of this family specific lipids that bind in this pocket are known these include cholesterol (STARD1/STARD3/ STARD4/STARD5) 25-hydroxycholesterol (STARD5) phosphatidylcholine (STARD2/ STARD7/STARD10) phosphatidylethanolamine (STARD10) and ceramides (STARD11). The START domain is found either alone or in association with other domains. Mammalian STARDs participate in the control of various cellular processes including lipid trafficking between intracellular compartments lipid metabolism and modulation of signaling events. Mutation or altered expression of STARDs is linked to diseases such as cancer genetic disorders and autoimmune disease. The Arabidopsis homeobox protein GLABRA 2 suppresses root hair formation in hairless epidermal root cells.
|