blastp_kegg |
lcl|rcu:RCOM_1176020
|
6 |
602 |
+ |
597 |
Gaps:3 |
99.00 |
600 |
82.66 |
0.0 |
Indole-3-acetic acid-amido synthetase GH3.5 putative
|
blastp_kegg |
lcl|fve:101311781
|
14 |
602 |
+ |
589 |
Gaps:3 |
99.15 |
591 |
81.74 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_kegg |
lcl|pmum:103329541
|
1 |
602 |
+ |
602 |
Gaps:6 |
99.83 |
597 |
81.04 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|tcc:TCM_007996
|
1 |
601 |
+ |
601 |
Gaps:8 |
95.81 |
621 |
81.51 |
0.0 |
Indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|pper:PRUPE_ppa003163mg
|
1 |
602 |
+ |
602 |
Gaps:6 |
99.83 |
597 |
80.70 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103947840
|
20 |
602 |
+ |
583 |
Gaps:3 |
98.47 |
589 |
81.72 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|mdm:103435463
|
20 |
602 |
+ |
583 |
Gaps:3 |
98.47 |
589 |
81.55 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5
|
blastp_kegg |
lcl|cic:CICLE_v10014670mg
|
21 |
601 |
+ |
581 |
Gaps:4 |
96.82 |
598 |
81.35 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102613332
|
21 |
601 |
+ |
581 |
Gaps:4 |
96.82 |
598 |
81.35 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_kegg |
lcl|vvi:100248306
|
11 |
602 |
+ |
592 |
Gaps:6 |
98.99 |
592 |
79.86 |
0.0 |
probable indole-3-acetic acid-amido synthetase GH3.5-like
|
blastp_uniprot_sprot |
sp|Q6I581|GH35_ORYSJ
|
20 |
602 |
+ |
583 |
Gaps:17 |
98.80 |
581 |
51.92 |
0.0 |
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|Q9SKE2|JAR1_ARATH
|
18 |
601 |
+ |
584 |
Gaps:21 |
98.61 |
575 |
50.44 |
0.0 |
Jasmonic acid-amido synthetase JAR1 OS Arabidopsis thaliana GN JAR1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q53P49|GH312_ORYSJ
|
16 |
601 |
+ |
586 |
Gaps:48 |
97.88 |
613 |
47.17 |
0.0 |
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
|
20 |
452 |
+ |
433 |
Gaps:20 |
90.26 |
462 |
49.16 |
1e-128 |
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|Q9FZ87|GH317_ARATH
|
26 |
598 |
+ |
573 |
Gaps:33 |
95.24 |
609 |
36.38 |
6e-125 |
Indole-3-acetic acid-amido synthetase GH3.17 OS Arabidopsis thaliana GN GH3.17 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O81829|GH35_ARATH
|
23 |
598 |
+ |
576 |
Gaps:24 |
93.46 |
612 |
36.54 |
2e-123 |
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
|
23 |
600 |
+ |
578 |
Gaps:27 |
93.39 |
605 |
36.46 |
5e-121 |
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
|
23 |
600 |
+ |
578 |
Gaps:27 |
93.39 |
605 |
36.46 |
5e-121 |
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|Q9LSQ4|GH36_ARATH
|
23 |
598 |
+ |
576 |
Gaps:24 |
93.46 |
612 |
35.84 |
2e-120 |
Indole-3-acetic acid-amido synthetase GH3.6 OS Arabidopsis thaliana GN GH3.6 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LYU4|GH312_ARATH
|
21 |
598 |
+ |
578 |
Gaps:43 |
98.96 |
575 |
37.26 |
4e-120 |
4-substituted benzoates-glutamate ligase GH3.12 OS Arabidopsis thaliana GN GH3.12 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|190600
|
21 |
587 |
+ |
567 |
Gaps:68 |
100.00 |
513 |
39.18 |
1e-139 |
pfam03321 GH3 GH3 auxin-responsive promoter.
|
rpsblast_cdd |
gnl|CDD|166261
|
23 |
589 |
+ |
567 |
Gaps:24 |
91.99 |
612 |
37.12 |
1e-115 |
PLN02620 PLN02620 indole-3-acetic acid-amido synthetase.
|
rpsblast_cdd |
gnl|CDD|165890
|
26 |
598 |
+ |
573 |
Gaps:34 |
95.21 |
606 |
36.22 |
1e-112 |
PLN02247 PLN02247 indole-3-acetic acid-amido synthetase.
|
rpsblast_cdd |
gnl|CDD|177891
|
23 |
600 |
+ |
578 |
Gaps:30 |
94.47 |
597 |
35.46 |
1e-107 |
PLN02249 PLN02249 indole-3-acetic acid-amido synthetase.
|