blastp_kegg |
lcl|pmum:103340001
|
10 |
347 |
+ |
338 |
Gaps:46 |
99.36 |
312 |
39.35 |
8e-51 |
putative B3 domain-containing protein Os03g0621600
|
blastp_kegg |
lcl|vvi:100255179
|
12 |
344 |
+ |
333 |
Gaps:66 |
96.67 |
390 |
35.01 |
8e-50 |
putative B3 domain-containing protein Os03g0621600-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa009270mg
|
10 |
347 |
+ |
338 |
Gaps:59 |
99.33 |
299 |
38.38 |
5e-41 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103965212
|
12 |
344 |
+ |
333 |
Gaps:49 |
81.23 |
357 |
36.21 |
7e-37 |
B3 domain-containing protein Os01g0723500-like
|
blastp_kegg |
lcl|fve:101304142
|
9 |
257 |
+ |
249 |
Gaps:29 |
96.67 |
240 |
40.52 |
3e-34 |
B3 domain-containing protein LOC_Os12g40080-like
|
blastp_kegg |
lcl|pmum:103326182
|
13 |
126 |
+ |
114 |
Gaps:2 |
37.84 |
296 |
53.57 |
1e-28 |
B3 domain-containing protein Os01g0723500-like
|
blastp_kegg |
lcl|mus:103975948
|
12 |
345 |
+ |
334 |
Gaps:32 |
91.78 |
353 |
29.63 |
2e-28 |
B3 domain-containing protein Os01g0723500-like
|
blastp_kegg |
lcl|fve:101308012
|
15 |
346 |
+ |
332 |
Gaps:103 |
96.85 |
508 |
34.76 |
2e-28 |
B3 domain-containing transcription factor VRN1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppb025337mg
|
1 |
120 |
+ |
120 |
Gaps:4 |
72.50 |
160 |
53.45 |
4e-28 |
hypothetical protein
|
blastp_kegg |
lcl|pda:103722010
|
12 |
344 |
+ |
333 |
Gaps:39 |
91.22 |
353 |
29.50 |
1e-27 |
B3 domain-containing protein Os01g0723500-like
|
blastp_pdb |
1yel_A
|
29 |
111 |
+ |
83 |
Gaps:2 |
77.88 |
104 |
39.51 |
9e-10 |
mol:protein length:104 At1g16640
|
blastp_uniprot_sprot |
sp|Q8S2E6|Y1235_ORYSJ
|
13 |
344 |
+ |
332 |
Gaps:83 |
90.30 |
402 |
27.55 |
3e-25 |
B3 domain-containing protein Os01g0723500 OS Oryza sativa subsp. japonica GN Os01g0723500 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q851V5|Y3216_ORYSJ
|
16 |
342 |
+ |
327 |
Gaps:101 |
65.50 |
1029 |
31.01 |
5e-24 |
Putative B3 domain-containing protein Os03g0621600 OS Oryza sativa subsp. japonica GN Os03g0621600 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8L3W1|VRN1_ARATH
|
28 |
344 |
+ |
317 |
Gaps:67 |
93.26 |
341 |
28.30 |
8e-21 |
B3 domain-containing transcription factor VRN1 OS Arabidopsis thaliana GN VRN1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q10GM3|Y3222_ORYSJ
|
17 |
330 |
+ |
314 |
Gaps:50 |
81.48 |
378 |
30.19 |
4e-19 |
B3 domain-containing protein Os03g0622200 OS Oryza sativa subsp. japonica GN Os03g0622200 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5JNA1|Y1237_ORYSJ
|
17 |
125 |
+ |
109 |
Gaps:12 |
15.72 |
719 |
38.94 |
3e-17 |
B3 domain-containing protein Os03g0120900 OS Oryza sativa subsp. japonica GN Os01g0723700 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FGD2|Y5698_ARATH
|
13 |
132 |
+ |
120 |
Gaps:7 |
36.83 |
334 |
39.84 |
7e-15 |
Putative B3 domain-containing protein At5g66980 OS Arabidopsis thaliana GN At5g66980 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q851V1|Y3160_ORYSJ
|
2 |
344 |
+ |
343 |
Gaps:65 |
96.08 |
306 |
28.57 |
8e-15 |
Putative B3 domain-containing protein Os03g0621600 OS Oryza sativa subsp. japonica GN Os03g0621600 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q2R9D2|Y1176_ORYSJ
|
28 |
344 |
+ |
317 |
Gaps:57 |
85.71 |
406 |
24.71 |
1e-14 |
B3 domain-containing protein Os11g0197600 OS Oryza sativa subsp. japonica GN Os11g0197600 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8RYD1|REM16_ARATH
|
17 |
329 |
+ |
313 |
Gaps:59 |
82.49 |
337 |
30.22 |
2e-14 |
B3 domain-containing protein REM16 OS Arabidopsis thaliana GN REM16 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q2QMT6|Y1208_ORYSJ
|
16 |
337 |
+ |
322 |
Gaps:45 |
61.02 |
490 |
26.42 |
3e-12 |
B3 domain-containing protein LOC_Os12g40080 OS Oryza sativa subsp. japonica GN Os12g0591400 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|197383
|
15 |
344 |
+ |
330 |
Gaps:16 |
100.00 |
98 |
48.98 |
1e-12 |
cd10017 B3_DNA Plant-specific B3-DNA binding domain. The plant-specific B3 DNA binding domain superfamily includes the well-characterized auxin response factor (ARF) and the LAV (Leafy cotyledon2 [LEC2]-Abscisic acid insensitive3 [ABI3]-VAL) families as well as the RAV (Related to ABI3 and VP1) and REM (REproductive Meristem) families. LEC2 and ABI3 have been shown to be involved in seed development while other members of the LAV family seem to have a more general role being expressed in many organs during plant development. Members of the ARF family bind to the auxin response element and depending on presence of an activation or repression domain they activate or repress transcription. RAV and REM families are less studied B3 protein famillies.
|
rpsblast_cdd |
gnl|CDD|202217
|
17 |
346 |
+ |
330 |
Gaps:22 |
100.00 |
97 |
45.36 |
3e-10 |
pfam02362 B3 B3 DNA binding domain. This is a family of plant transcription factors with various roles in development the aligned region corresponds the B3 DNA binding domain as described in this domain is found in VP1/AB13 transcription factors. Some proteins also have a second AP2 DNA binding domain pfam00847 such as RAV1. DNA binding activity was demonstrated by.
|
rpsblast_cdd |
gnl|CDD|198087
|
17 |
345 |
+ |
329 |
Gaps:16 |
100.00 |
96 |
42.71 |
3e-09 |
smart01019 B3 B3 DNA binding domain. Two DNA binding proteins RAV1 and RAV2 from Arabidopsis thaliana contain two distinct amino acid sequence domains found only in higher plant species. The N-terminal regions of RAV1 and RAV2 are homologous to the AP2 DNA-binding domain (see ) present in a family of transcription factors while the C-terminal region exhibits homology to the highly conserved C-terminal domain designated B3 of VP1/ABI3 transcription factors. The AP2 and B3-like domains of RAV1 bind autonomously to the CAACA and CACCTG motifs respectively and together achieve a high affinity and specificity of binding. It has been suggested that the AP2 and B3-like domains of RAV1 are connected by a highly flexible structure enabling the two domains to bind to the CAACA and CACCTG motifs in various spacings and orientations.
|