← Back to Repository
BGC0000125PKS

Pimaricin

Producing organism
Streptomyces natalensis
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Unknown)
Total steps
16
DOI
MIBiG entry
View on MIBiG ↗
Loading…
pimaricin
C33H47NO13665.30 Da

Gene Cluster Map17 genes · 84,985 bp

KSKSKSKSKSKSKSKSAKSKSKSKSKS20 kb85.0 kb visible · 84,985 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Other
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
KRKetoreductase (KR)
ACPAcyl carrier protein (ACP)
ACPAcyl carrier (ACP)
AAdenylation (A)
TEThioesterase (TE)
DnDocking N-term
DcDocking C-term
AmTAminotransferase V

Pathway Graphsteps arranged in biosynthetic order

16 steps · 15 edges
Step 1Load
pimS0
+Acetyl-CoA
Inactive: KS
Step 15
Start
+Mycosamine
Step 2M1
pimS1
+Malonyl-CoA
Step 3M2
pimS1
+Malonyl-CoA
Step 4M3
pimS1
+Malonyl-CoA
Step 5M4
pimS1
+Malonyl-CoA
Step 6M5
pimS2
+Malonyl-CoA
Step 7M6
pimS2
+Malonyl-CoA
Step 8M7
pimS2
+Methylmalonyl-CoA
Step 9M8
pimS2
+Malonyl-CoA
Step 10M9
pimS2
+Malonyl-CoA
Inactive: KR
Step 11M10
pimS2
+Malonyl-CoA
Step 12M11
pimS3
+Malonyl-CoA
Step 13M12
pimS4
+Malonyl-CoA
Step 14TE
pimS4
Step 16
pimK
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions16 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1125-1pimS0Loading
Acetyl-CoA
O=C(O)C{'Inactive': ['KS']}
2125-2pimS1M1
125-1;Malonyl-CoA
from: 125-1
OC(CC(O)=O)C
3125-3pimS1M2
125-2;Malonyl-CoA
from: 125-2
OC(C/C=C/C(O)=O)C
4125-4pimS1M3
125-3;Malonyl-CoA
from: 125-3
OC(C/C=C/C=C/C(O)=O)C
5125-5pimS1M4
125-4;Malonyl-CoA
from: 125-4
OC(C/C=C/C=C/C=C/C(O)=O)C
6125-6pimS2M5
125-5;Malonyl-CoA
from: 125-5
OC(C/C=C/C=C/C=C/C=C/C(O)=O)C
7125-7pimS2M6
125-6;Malonyl-CoA
from: 125-6
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)=O)C
8125-8pimS2M7
125-7;Methylmalonyl-CoA
from: 125-7
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)=O)C)C
9125-9pimS2M8
125-8;Malonyl-CoA
from: 125-8
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)CC(O)=O)C)C
10125-10pimS2M9
125-9;Malonyl-CoA
from: 125-9
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)CC(CC(O)=O)=O)C)C{'Inactive': ['KR']}
11125-11pimS2M10
125-10;Malonyl-CoA
from: 125-10
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)CC(CC(O)CC(O)=O)=O)C)C
12125-12pimS3M11
125-11;Malonyl-CoA
from: 125-11
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)CC(CC(O)C/C=C/C(O)=O)=O)C)C
13125-13pimS4M12
125-12;Malonyl-CoA
from: 125-12
OC(C/C=C/C=C/C=C/C=C/C(O)CC(O)C(C(O)CC(CC(O)C/C=C/C=C/C(O)=O)=O)C)C
14125-14pimS4TE
125-13
from: 125-13
OC(CC(O1)C1/C=C/C(OC(C)C/C=C/C=C/C=C/C=C/C(O)C2)=O)CC3(O)OC2C(C(O)=O)C(O)C3
15125-15Start
Mycosamine
OC1C(O)C(N)C(O)C(C)O1
16125pimK
125-14;125-15
from: 125-14, 125-15
OC(CC(O1)C1/C=C/C(OC(C)C/C=C/C=C/C=C/C=C/C(OC2C(O)C(N)C(O)C(C)O2)C3)=O)CC4(O)OC3C(C(O)=O)C(O)C4
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture