blastp_kegg |
lcl|vvi:100262428
|
30 |
498 |
+ |
469 |
Gaps:2 |
94.18 |
498 |
63.97 |
0.0 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|vvi:100267583
|
30 |
498 |
+ |
469 |
Gaps:1 |
94.38 |
498 |
62.98 |
0.0 |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|vvi:100245281
|
30 |
495 |
+ |
466 |
Gaps:4 |
89.71 |
515 |
61.47 |
0.0 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|rcu:RCOM_1574420
|
29 |
497 |
+ |
469 |
none |
94.56 |
496 |
51.81 |
2e-179 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme putative (EC:1.14.13.71)
|
blastp_kegg |
lcl|sot:102579029
|
34 |
498 |
+ |
465 |
Gaps:2 |
94.34 |
495 |
54.82 |
6e-178 |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|vvi:100249676
|
26 |
498 |
+ |
473 |
Gaps:1 |
95.37 |
497 |
51.69 |
5e-177 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 1-like
|
blastp_kegg |
lcl|rcu:RCOM_1684370
|
34 |
495 |
+ |
462 |
Gaps:1 |
92.42 |
501 |
54.43 |
6e-176 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme putative (EC:1.14.13.71)
|
blastp_kegg |
lcl|sly:101244980
|
39 |
498 |
+ |
460 |
Gaps:3 |
93.35 |
496 |
55.08 |
2e-173 |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|vvi:100244525
|
30 |
498 |
+ |
469 |
Gaps:2 |
82.49 |
571 |
51.80 |
2e-172 |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_kegg |
lcl|vvi:100247960
|
48 |
498 |
+ |
451 |
Gaps:8 |
89.66 |
503 |
54.32 |
3e-171 |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2-like
|
blastp_pdb |
3pm0_A
|
40 |
487 |
+ |
448 |
Gaps:50 |
91.52 |
507 |
28.23 |
2e-42 |
mol:protein length:507 Cytochrome P450 1B1
|
blastp_pdb |
3swz_D
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3swz_C
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3swz_B
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3swz_A
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3ruk_D
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3ruk_C
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3ruk_B
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
3ruk_A
|
40 |
466 |
+ |
427 |
Gaps:56 |
89.27 |
494 |
28.80 |
7e-39 |
mol:protein length:494 Steroid 17-alpha-hydroxylase/17 20 lyase
|
blastp_pdb |
2hi4_A
|
40 |
485 |
+ |
446 |
Gaps:35 |
92.73 |
495 |
25.05 |
4e-37 |
mol:protein length:495 Cytochrome P450 1A2
|
blastp_uniprot_sprot |
sp|Q9FXW4|C80B2_COPJA
|
34 |
497 |
+ |
464 |
Gaps:5 |
94.47 |
488 |
49.46 |
1e-128 |
Probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2 OS Coptis japonica GN CYP80B2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64900|C80B2_ESCCA
|
39 |
497 |
+ |
459 |
Gaps:6 |
94.06 |
488 |
44.66 |
5e-125 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 2 OS Eschscholzia californica GN CYP80B2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64899|C80B1_ESCCA
|
39 |
497 |
+ |
459 |
Gaps:6 |
94.25 |
487 |
43.79 |
3e-124 |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 1 (Fragment) OS Eschscholzia californica GN CYP80B1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P47195|C80A1_BERST
|
13 |
497 |
+ |
485 |
Gaps:29 |
96.92 |
487 |
41.95 |
1e-120 |
Berbamunine synthase OS Berberis stolonifera GN CYP80A1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8VWZ7|C76B6_CATRO
|
14 |
494 |
+ |
481 |
Gaps:18 |
98.38 |
493 |
40.41 |
2e-117 |
Geraniol 8-hydroxylase OS Catharanthus roseus GN CYP76B6 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64635|C76C4_ARATH
|
39 |
494 |
+ |
456 |
Gaps:19 |
91.39 |
511 |
40.90 |
3e-115 |
Cytochrome P450 76C4 OS Arabidopsis thaliana GN CYP76C4 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O64637|C76C2_ARATH
|
48 |
498 |
+ |
451 |
Gaps:30 |
90.43 |
512 |
41.25 |
8e-113 |
Cytochrome P450 76C2 OS Arabidopsis thaliana GN CYP76C2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64636|C76C1_ARATH
|
13 |
498 |
+ |
486 |
Gaps:21 |
97.46 |
512 |
38.68 |
4e-112 |
Cytochrome P450 76C1 OS Arabidopsis thaliana GN CYP76C1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|D1MI46|C76BA_SWEMU
|
49 |
493 |
+ |
445 |
Gaps:13 |
90.91 |
495 |
41.11 |
4e-110 |
Geraniol 8-hydroxylase OS Swertia mussotii GN CYP76B10 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O23976|C76B1_HELTU
|
39 |
494 |
+ |
456 |
Gaps:15 |
93.67 |
490 |
42.48 |
3e-105 |
7-ethoxycoumarin O-deethylase OS Helianthus tuberosus GN CYP76B1 PE 1 SV 1
|