← Back to Repository
BGC0000148PKS

A83543A;Spinosyn D

Producing organism
Saccharopolyspora spinosa
Taxonomy
BacteriaActinomycetotaActinomycetesPseudonocardialesPseudonocardiaceaeSaccharopolyspora
Biosynthetic class
PKS (Type I)
Total steps
27
DOI
MIBiG entry
View on MIBiG ↗
Loading…
C41H65NO10731.46 Da

Gene Cluster Map23 genes · 80,161 bp

KSKSKSKSKSKSKSKSKSKSKS20 kb80.2 kb visible · 80,161 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
EREnoylreductase (ER)
KRKetoreductase (KR)
ACPAcyl carrier protein (ACP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
DnDocking N-term
DcDocking C-term
MTMethyltransferase
BELBeta-elim. lyase
AmTAminotransferase I/II

Pathway Graphsteps arranged in biosynthetic order

27 steps · 27 edges
Step 1
Start
+Methylmalonyl-CoA
Step 15
Start
+D-glucose-1-phosp…
Step 2Load
spnA
Step 16
?
Step 3M1
spnA
+Malonyl-CoA
Step 17
?
Step 4M2
spnB
+Malonyl-CoA
Step 18
?
Step 20
spnO
Step 5M3
spnC
+Methylmalonyl-CoA
Step 19
?
Step 21
spnN
Step 6M4
spnC
+Malonyl-CoA
Step 22
spnQ, spnR
Step 7M5
spnD
+Malonyl-CoA
Step 23
spnS
Step 8M6
spnD
+Malonyl-CoA
Step 9M7
spnD
+Malonyl-CoA
Step 10M8
spnE
+Malonyl-CoA
Step 11M9
spnE
+Malonyl-CoA
Step 12M10
spnE
+Malonyl-CoA
Step 13TE
spnE
Step 14
spnF, spnJ, spnL, spnM
Step 24
spnG
Step 25
spnK, spnI, spnH
Step 26
spnP
Step 27
?
+148(1)
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions27 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1148-1Start
Methylmalonyl-CoA
O=C([R])CC
2148-2spnALoading
148-1
from: 148-1
O=C(O)CC
3148-3spnAM1
148-2;Malonyl-CoA
from: 148-2
OC(CC(O)=O)CC
4148-4spnBM2
148-3;Malonyl-CoA
from: 148-3
OC(CCCC(O)=O)CC
5148-5spnCM3
148-4;Methylmalonyl-CoA
from: 148-4
OC(CCCC(O)C(C)C(O)=O)CC
6148-6spnCM4
148-5;Malonyl-CoA
from: 148-5
OC(CCCC(O)C(C)C(O)CC(O)=O)CC
7148-7spnDM5
148-6;Malonyl-CoA
from: 148-6
OC(CCCC(O)C(C)C(O)C/C=C/C(O)=O)CC
8148-8spnDM6
148-7;Malonyl-CoA
from: 148-7
OC(CCCC(O)C(C)C(O)C/C=C/C(O)CC(O)=O)CC
9148-9spnDM7
148-8;Malonyl-CoA
from: 148-8
OC(CCCC(O)C(C)C(O)C/C=C/C(O)CC(O)CC(O)=O)CC
10148-10spnEM8
148-9;Malonyl-CoA
from: 148-9
OC(CCCC(O)C(C)C(O)C/C=C/C(O)CC(O)C/C=C/C(O)=O)CC
11148-11spnEM9
148-10;Malonyl-CoA
from: 148-10
OC(CCCC(O)C(C)C(O)C/C=C/C(O)CC(O)C/C=C/C=C/C(O)=O)CC
12148-12spnEM10
148-11;Malonyl-CoA
from: 148-11
OC(CCCC(O)C(C)C(O)C/C=C/C(O)CC(O)C/C=C/C=C/C=C/C(O)=O)CC
13148-13spnETE
148-12
from: 148-12
OC1C/C=C/C=C/C=C/C(OC(CC)CCCC(O)C(C)C(O)C/C=C/C(O)C1)=O
14148-14spnF, spnJ, spnL, spnM
148-13
from: 148-13
OC1CC2C=CC3C4C(C(C(C)C(O)CCCC(CC)OC(C4)=O)=O)=CC3C2C1
15148-15Start
D-glucose-1-phosphate
O[C@H]1[C@H](O)[C@@H](O)[C@@H](OP([O-])([O-])=O)O[C@@H]1CO
16148-16?
148-15
from: 148-15
O[C@H]1[C@H](O)[C@@H](O)[C@@H]([R])O[C@@H]1CO
17148-17?
148-16
from: 148-16
O[C@H]([C@@H](O)[C@@H]([R])O[C@@H]1C)C1=O
18148-18?
148-17
from: 148-17
O[C@@H]([C@@H]([R])O[C@H]1C)[C@H](O)C1=O
19148-19?
148-18
from: 148-18
O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@@H]1[R]
20148-20spnO
148-17
from: 148-17
C[C@H]1O[C@H]([R])CC(C1=O)=O
21148-21spnN
148-20
from: 148-20
C[C@H]1O[C@H]([R])C[C@@H](O)C1=O
22148-22spnQ, spnR
148-21
from: 148-21
C[C@H]1O[C@H]([R])CCC1N
23148-23spnS
148-22
from: 148-22
C[C@H]1O[C@H]([R])CCC1N(C)C
24148-24spnG
148-14;148-19
from: 148-14, 148-19
CCC(OC(CC1C2C3C4CC(O[C@@H]([C@H]5O)O[C@@H](C)C(O)[C@@H]5O)CC4C=C2)=O)CCCC(O)C(C)C(C1=C3)=O
25148-25spnK, spnI, spnH
148-24
from: 148-24
CCC(OC(CC1C2C3C4CC(O[C@@H]([C@H]5OC)O[C@@H](C)C(OC)[C@@H]5OC)CC4C=C2)=O)CCCC(O)C(C)C(C1=C3)=O
26148(1)spnP
148-25;148-23
from: 148-25, 148-23
CCC(OC(CC1C2C3C4CC(O[C@@H]([C@H]5OC)O[C@@H](C)C(OC)[C@@H]5OC)CC4C=C2)=O)CCCC(O[C@@H]6CCC(N(C)C)[C@@H](C)O6)C(C)C(C1=C3)=O
27148(2)?
148(1)
CCC(OC(CC1C2C3C4CC(O[C@@H]([C@H]5OC)O[C@@H](C)C(OC)[C@@H]5OC)CC4C(C)=C2)=O)CCCC(O[C@@H]6CCC(N(C)C)[C@@H](C)O6)C(C)C(C1=C3)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture