blastp_kegg |
lcl|gmx:102664111
|
1 |
92 |
+ |
92 |
Gaps:1 |
90.29 |
103 |
74.19 |
6e-42 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_kegg |
lcl|cmo:103483208
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.52 |
575 |
78.95 |
7e-41 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|csv:101212037
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.61 |
572 |
78.95 |
9e-41 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa003388mg
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.41 |
579 |
78.95 |
9e-41 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103965897
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.64 |
571 |
76.84 |
1e-40 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|pmum:103332267
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.41 |
579 |
78.95 |
1e-40 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|mdm:103413018
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.64 |
571 |
75.79 |
1e-40 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|mdm:103417626
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.64 |
571 |
75.79 |
2e-40 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|gmx:100777944
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.64 |
571 |
74.74 |
1e-39 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_kegg |
lcl|mdm:103439296
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.64 |
571 |
73.68 |
3e-39 |
jasmonic acid-amido synthetase JAR1-like
|
blastp_uniprot_sprot |
sp|Q6I581|GH35_ORYSJ
|
6 |
94 |
+ |
89 |
none |
15.32 |
581 |
61.80 |
4e-32 |
Probable indole-3-acetic acid-amido synthetase GH3.5 OS Oryza sativa subsp. japonica GN GH3.5 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q53P49|GH312_ORYSJ
|
1 |
94 |
+ |
94 |
none |
15.33 |
613 |
57.45 |
6e-29 |
Probable indole-3-acetic acid-amido synthetase GH3.12 OS Oryza sativa subsp. japonica GN GH3.12 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5NAZ7|GH33_ORYSJ
|
7 |
94 |
+ |
88 |
Gaps:1 |
19.26 |
462 |
62.92 |
7e-29 |
Probable indole-3-acetic acid-amido synthetase GH3.3 OS Oryza sativa subsp. japonica GN GH3.3 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9SKE2|JAR1_ARATH
|
1 |
94 |
+ |
94 |
Gaps:3 |
16.87 |
575 |
54.64 |
2e-23 |
Jasmonic acid-amido synthetase JAR1 OS Arabidopsis thaliana GN JAR1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|O81829|GH35_ARATH
|
1 |
88 |
+ |
88 |
none |
14.38 |
612 |
42.05 |
2e-16 |
Indole-3-acetic acid-amido synthetase GH3.5 OS Arabidopsis thaliana GN GH3.5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q0D4Z6|GH38_ORYSJ
|
1 |
88 |
+ |
88 |
none |
14.55 |
605 |
42.05 |
9e-16 |
Probable indole-3-acetic acid-amido synthetase GH3.8 OS Oryza sativa subsp. japonica GN GH3.8 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A3BLS0|GH38_ORYSI
|
1 |
88 |
+ |
88 |
none |
14.55 |
605 |
42.05 |
9e-16 |
Probable indole-3-acetic acid-amido synthetase GH3.8 OS Oryza sativa subsp. indica GN GH3.8 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q6ZLA7|GH310_ORYSJ
|
2 |
87 |
+ |
86 |
Gaps:1 |
18.20 |
478 |
43.68 |
1e-14 |
Putative indole-3-acetic acid-amido synthetase GH3.10 OS Oryza sativa subsp. japonica GN GH3.10 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8LQM5|GH31_ORYSJ
|
8 |
88 |
+ |
81 |
Gaps:2 |
13.61 |
610 |
45.78 |
2e-14 |
Probable indole-3-acetic acid-amido synthetase GH3.1 OS Oryza sativa subsp. japonica GN GH3.1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P0C0M2|GH32_ORYSJ
|
3 |
88 |
+ |
86 |
none |
14.01 |
614 |
44.19 |
4e-14 |
Probable indole-3-acetic acid-amido synthetase GH3.2 OS Oryza sativa subsp. japonica GN GH3.2 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|190600
|
11 |
94 |
+ |
84 |
Gaps:1 |
16.18 |
513 |
43.37 |
1e-20 |
pfam03321 GH3 GH3 auxin-responsive promoter.
|
rpsblast_cdd |
gnl|CDD|166261
|
8 |
88 |
+ |
81 |
Gaps:1 |
13.40 |
612 |
45.12 |
1e-16 |
PLN02620 PLN02620 indole-3-acetic acid-amido synthetase.
|
rpsblast_cdd |
gnl|CDD|177891
|
3 |
88 |
+ |
86 |
none |
14.41 |
597 |
40.70 |
6e-13 |
PLN02249 PLN02249 indole-3-acetic acid-amido synthetase.
|
rpsblast_cdd |
gnl|CDD|165890
|
12 |
90 |
+ |
79 |
Gaps:1 |
12.87 |
606 |
39.74 |
2e-12 |
PLN02247 PLN02247 indole-3-acetic acid-amido synthetase.
|