| CAM34356.1 |
putative_FAD-depending_monooxygenase |
BGC0000242.5 |
PKS |
33.0 |
94.8 |
125.0 |
4.16e-32 |
| AFW04593.1 |
FAD-dependent_oxidoreductase |
BGC0001783.5 |
other:other |
31.0 |
93.4 |
119.0 |
7.8e-30 |
| AAG06716.1 |
probable_FAD-dependent_monooxygenase |
BGC0002037.3 |
NRPS:Type I |
32.0 |
91.6 |
115.0 |
1.54e-28 |
| OKJ62000.1 |
FAD-dependent_monooxygenase |
BGC0002147.2 |
NRPS:Type I |
29.0 |
92.7 |
103.0 |
4.01e-24 |
| AEW95635.1 |
FAD-dependent_monooxygenase |
BGC0002697.3 |
NRPS:Type I+PKS |
29.0 |
89.0 |
100.0 |
3.85e-23 |
| AAP85357.1 |
putative_monooxygenase |
BGC0000233.5 |
PKS |
31.0 |
95.8 |
100.0 |
7.86e-23 |
| RZB16712.1 |
FAD-binding_protein |
BGC0001850.4 |
other:shikimate-derived |
30.0 |
86.4 |
94.0 |
9.32e-21 |
| QJS40191.1 |
PhzS |
BGC0002439.3 |
other:other |
29.0 |
97.4 |
88.0 |
1.03e-18 |
| AFW04561.1 |
oxidoreductase |
BGC0001783.5 |
other:other |
28.0 |
94.2 |
87.0 |
1.26e-18 |
| AXO35220.1 |
putative_n-hydroxybenzoate_hydroxylase |
BGC0001848.4 |
other:other |
29.0 |
95.8 |
87.0 |
1.69e-18 |
| UHY14128.1 |
FAD-dependent_monooxygenase |
BGC0002671.2 |
PKS |
30.0 |
89.5 |
87.0 |
2.09e-18 |
| AGP37409.1 |
hypothetical_protein |
BGC0002386.2 |
NRPS:Type I+PKS |
27.0 |
91.9 |
79.0 |
9.32e-16 |
| CAQ52625.1 |
FAD-dependent_monooxygenase |
BGC0001066.5 |
PKS:Type I |
26.0 |
86.1 |
73.0 |
9.35e-14 |
| AMK51267.1 |
Hex10 |
BGC0001376.5 |
PKS |
27.0 |
110.0 |
63.0 |
1.86e-10 |
| ACZ87068.1 |
putative_monoxygenase |
BGC0002732.3 |
PKS |
27.0 |
108.4 |
61.0 |
5.87e-10 |
| OBR09783.1 |
FAD_binding_domain-containing_protein |
BGC0002429.3 |
PKS:Type I+terpene:Diterpene |
25.0 |
101.6 |
61.0 |
8.76e-10 |
| CBF83145.1 |
conserved_hypothetical_protein |
BGC0001722.3 |
PKS |
25.0 |
87.9 |
57.0 |
1.19e-08 |
| BDO47155.1 |
FAD-dependent_monooxygenase_BrvE |
BGC0002759.2 |
terpene:Sesquiterpene+PKS:Iterative type I |
25.0 |
90.0 |
54.0 |
1.46e-07 |
| CAP12596.1 |
TcmB2_oxygenase |
BGC0000219.4 |
PKS:Type II+saccharide:hybrid/tailoring |
26.0 |
90.3 |
52.0 |
8.6e-07 |