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BGC0002808PKS

N-coronafacoyl-L-isoleucine

Producing organism
Streptomyces scabiei 87.22
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Type I)
Total steps
11
DOI
MIBiG entry
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N-coronafacoyl-L-isoleucine

Gene Cluster Map15 genes · 31,376 bp

KSAATKSATDHERKRKSATDHERKRTEAERKR5 kb31.4 kb visible · 31,376 bp total
Biosynthetic (core)
Biosynthetic (additional)
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
EREnoylreductase (ER)
KRKetoreductase (KR)
ACPAcyl carrier protein (ACP)
ACPAcyl carrier (ACP)
AAdenylation (A)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
DcDocking C-term

Pathway Graphsteps arranged in biosynthetic order

11 steps · 10 edges
Step 1
SCAB_79601, SCAB_79611,…
+?, Malonyl-CoA
Step 2
Start
+Hydroxybutyryl-CoA
Step 3
SCAB_79711
Step 4
SCAB_79701
Step 5
SCAB_79651
Step 6
SCAB_79661
+Malonyl-CoA
Inactive: ER
Step 7TE
SCAB_79661
{'Domain_Reuse': ['SCAB_79…
Step 8
SCAB_79681?
Step 9
SCAB_79691
Step 10
SCAB_79721
Step 11
SCAB_79671
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions11 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
12808-1SCAB_79601, SCAB_79611, SCAB_79621, SCAB_79631, SCAB_79641
?;Malonyl-CoA
OC(C1=CCCC1)=O
22808-2Start
Hydroxybutyryl-CoA
C[C@@H](CC([R])=O)O
32808-3SCAB_79711
2808-2
from: 2808-2
C/C=C/C([R])=O
42808-4SCAB_79701
2808-3
from: 2808-3
CCCC([R])=O
52808-5SCAB_79651
2808-1;2808-4
from: 2808-1, 2808-4
CC[C@@H](C(O)=O)CC1=CCCC1
62808-6SCAB_79661
2808-5;Malonyl-CoA
from: 2808-5
CC[C@@H](C(CC(O)=O)=O)CC1=CCCC1{'Inactive': ['ER']}
72808-7SCAB_79661TE
2808-6
from: 2808-6
[H][C@@]12[C@@](CCC2)([H])C(C(O)=O)C[C@H](CC)C1{'Domain_Reuse': ['SCAB_7966…
82808-8SCAB_79681?
2808-7
from: 2808-7
[H][C@@]12[C@@](CCC2)([H])C(C(O)=O)=C[C@H](CC)C1
92808-9SCAB_79691
2808-8
from: 2808-8
[H][C@@]12[C@@](CC[C@H]2O)([H])C(C(O)=O)=C[C@H](CC)C1
102808-10SCAB_79721
2808-9
from: 2808-9
[H][C@@]12[C@@](CCC2=O)([H])C(C(O)=O)=C[C@H](CC)C1
112808SCAB_79671
2808-10
from: 2808-10
[H][C@@]12[C@@](CCC2=O)([H])C(C(NC(C(O)=O)[C@@H](C)CC)=O)=C[C@H](CC)C1
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture