blastp_kegg |
lcl|pop:POPTR_0008s03430g
|
3 |
275 |
+ |
273 |
Gaps:7 |
65.87 |
419 |
55.07 |
6e-94 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0008s03350g
|
3 |
275 |
+ |
273 |
Gaps:9 |
61.99 |
442 |
55.84 |
1e-92 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_0253460
|
2 |
278 |
+ |
277 |
Gaps:10 |
62.61 |
452 |
52.30 |
1e-90 |
Anthranilate N-benzoyltransferase protein putative (EC:2.3.1.150)
|
blastp_kegg |
lcl|pop:POPTR_0008s03420g
|
9 |
278 |
+ |
270 |
Gaps:9 |
56.47 |
487 |
53.82 |
1e-87 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0008s03410g
|
3 |
278 |
+ |
276 |
Gaps:7 |
62.42 |
447 |
50.90 |
3e-84 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101299970
|
4 |
277 |
+ |
274 |
Gaps:10 |
61.57 |
458 |
49.29 |
1e-83 |
vinorine synthase-like
|
blastp_kegg |
lcl|rcu:RCOM_0721180
|
2 |
278 |
+ |
277 |
Gaps:7 |
63.21 |
443 |
48.57 |
3e-82 |
Anthranilate N-benzoyltransferase protein putative (EC:2.3.1.150)
|
blastp_kegg |
lcl|tcc:TCM_043311
|
19 |
280 |
+ |
262 |
Gaps:13 |
78.60 |
584 |
51.85 |
5e-76 |
HXXXD-type acyl-transferase family protein putative
|
blastp_kegg |
lcl|rcu:RCOM_0355370
|
1 |
277 |
+ |
277 |
Gaps:9 |
62.64 |
447 |
46.79 |
2e-72 |
Anthranilate N-benzoyltransferase protein putative (EC:2.3.1.150)
|
blastp_kegg |
lcl|cic:CICLE_v10011699mg
|
2 |
277 |
+ |
276 |
Gaps:14 |
62.25 |
453 |
44.68 |
2e-68 |
hypothetical protein
|
blastp_pdb |
2bgh_B
|
1 |
261 |
+ |
261 |
Gaps:27 |
57.01 |
421 |
35.83 |
3e-30 |
mol:protein length:421 VINORINE SYNTHASE
|
blastp_pdb |
2bgh_A
|
1 |
261 |
+ |
261 |
Gaps:27 |
57.01 |
421 |
35.83 |
3e-30 |
mol:protein length:421 VINORINE SYNTHASE
|
blastp_uniprot_sprot |
sp|Q70PR7|VINSY_RAUSE
|
1 |
261 |
+ |
261 |
Gaps:27 |
57.01 |
421 |
35.83 |
1e-29 |
Vinorine synthase OS Rauvolfia serpentina GN ACT PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9FI40|BAHD1_ARATH
|
1 |
279 |
+ |
279 |
Gaps:13 |
63.66 |
443 |
30.85 |
3e-29 |
BAHD acyltransferase At5g47980 OS Arabidopsis thaliana GN BAHD1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9ZTK5|DAT_CATRO
|
1 |
272 |
+ |
272 |
Gaps:27 |
62.19 |
439 |
27.47 |
4e-20 |
Deacetylvindoline O-acetyltransferase OS Catharanthus roseus GN DAT PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64988|BEATH_CLABR
|
1 |
272 |
+ |
272 |
Gaps:36 |
63.28 |
433 |
26.28 |
3e-19 |
Acetyl-CoA-benzylalcohol acetyltransferase OS Clarkia breweri GN BEAT PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SPU3|BEATL_CLABR
|
1 |
272 |
+ |
272 |
Gaps:36 |
63.28 |
433 |
25.91 |
1e-18 |
Acetyl-CoA-benzylalcohol acetyltransferase OS Clarkia breweri GN BEAT PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q94FT4|SALAT_PAPSO
|
1 |
262 |
+ |
262 |
Gaps:60 |
62.03 |
474 |
29.59 |
1e-17 |
Salutaridinol 7-O-acetyltransferase OS Papaver somniferum GN SALAT PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6TXD2|5MAT2_SALSN
|
1 |
272 |
+ |
272 |
Gaps:31 |
63.07 |
417 |
27.76 |
5e-14 |
Pelargonidin 3-O-(6-caffeoylglucoside) 5-O-(6-O-malonylglucoside) 4'''-malonyltransferase OS Salvia splendens PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A9ZPJ7|AGCT2_HORVU
|
52 |
263 |
+ |
212 |
Gaps:28 |
48.29 |
439 |
27.36 |
5e-07 |
Agmatine coumaroyltransferase-2 OS Hordeum vulgare GN ACT-2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A9ZPJ6|AGCT1_HORVU
|
52 |
263 |
+ |
212 |
Gaps:28 |
48.29 |
439 |
27.36 |
6e-07 |
Agmatine coumaroyltransferase-1 OS Hordeum vulgare GN ACT-1 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|165708
|
1 |
278 |
+ |
278 |
Gaps:7 |
62.84 |
444 |
53.41 |
7e-92 |
PLN00140 PLN00140 alcohol acetyltransferase family protein Provisional.
|
rpsblast_cdd |
gnl|CDD|111364
|
1 |
268 |
+ |
268 |
Gaps:42 |
62.50 |
432 |
29.26 |
5e-29 |
pfam02458 Transferase Transferase family. This family includes a number of transferase enzymes. These include anthranilate N-hydroxycinnamoyl/benzoyltransferase that catalyzes the first committed reaction of phytoalexin biosynthesis. Deacetylvindoline 4-O-acetyltransferase EC:2.3.1.107 catalyzes the last step in vindoline biosynthesis is also a member of this family. The motif HXXXD is probably part of the active site. The family also includes trichothecene 3-O-acetyltransferase.
|