← Back to Repository
BGC0000060PKS

Fostriecin

Producing organism
Streptomyces pulveraceus
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Unknown)
Total steps
15
DOI
MIBiG entry
View on MIBiG ↗
Loading…
fostriecin
C19H27O9P430.14 Da

Gene Cluster Map21 genes · 73,577 bp

KSKSKSKSKSKSKSKSKS10 kb73.6 kb visible · 73,577 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
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
DHtDehydratase (DHt)
MTMethyltransferase

Pathway Graphsteps arranged in biosynthetic order

15 steps · 14 edges
Step 1Load
fosA
+Malonyl-CoA
Step 10
Start
Step 2M1
fosA
+Malonyl-CoA
Inactive: ER
Step 3M2
fosB
+Malonyl-CoA
Step 4M3
fosC
+Malonyl-CoA
Step 5M4
fosC
+Malonyl-CoA
Step 6M5
fosD
+Methylmalonyl-CoA
Step 7M6
fosE
+Malonyl-CoA
Step 8M7
fosE
+Malonyl-CoA
Step 9M8
fosF
+Malonyl-CoA
Step 11TE
fosF
Step 12
fosJ
Step 13
fosH
Step 14
fosK
Step 15
fosM
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions15 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
160-1fosALoading
Malonyl-CoA
O=C(C)O
260-2fosAM1
60-1;Malonyl-CoA
from: 60-1
C/C=C/C(O)=O{'Inactive': ['ER']}
360-3fosBM2
60-2;Malonyl-CoA
from: 60-2
O=C(O)/C=C\C=C\C
460-4fosCM3
60-3;Malonyl-CoA
from: 60-3
O=C(O)/C=C\C=C/C=C/C
560-5fosCM4
60-4;Malonyl-CoA
from: 60-4
C/C=C/C=C\C=C/[C@H](O)CC(O)=O
660-6fosDM5
60-5;Methylmalonyl-CoA
from: 60-5
C/C=C/C=C\C=C/[C@H](O)C[C@@H](O)[C@@H](C)C(O)=O
760-7fosEM6
60-6;Malonyl-CoA
from: 60-6
C/C=C/C=C\C=C/[C@H](O)C[C@@H](O)[C@@H](C)/C=C/C(O)=O
860-8fosEM7
60-7;Malonyl-CoA
from: 60-7
C/C=C/C=C\C=C/[C@H](O)C[C@@H](O)[C@@H](C)/C=C/[C@H](O)CC(O)=O
960-9fosFM8
60-8;Malonyl-CoA
from: 60-8
C/C=C/C=C\C=C/[C@H](O)C[C@@H](O)[C@@H](C)/C=C/[C@H](O)CC(O)CC(O)=O
1060-10Start
O=C(CC(O)=O)O
1160-11fosFTE
60-9;60-10
from: 60-9, 60-10
O=C(CC(O)=O)OC(C1)C[C@H](/C=C/[C@H](C)[C@H](O)C[C@@H](O)/C=C\C=C/C=C/C)OC1=O
1260-12fosJ
60-11
from: 60-11
O=C(CC(O)=O)OC(C1)C[C@H](/C=C/[C@@](C)(O)[C@H](O)C[C@@H](O)/C=C\C=C/C=C/C)OC1=O
1360-13fosH
60-12
from: 60-12
O=C(CC(O)=O)OC(C1)C[C@H](/C=C/[C@@](C)(O)[C@H](OP(O)(O)=O)C[C@@H](O)/C=C\C=C/C=C/C)OC1=O
1460-14fosK
60-13
from: 60-13
O=C(CC(O)=O)OC(C1)C[C@H](/C=C/[C@@](C)(O)[C@H](OP(O)(O)=O)C[C@@H](O)/C=C\C=C/C=C/CO)OC1=O
1560fosM
60-14
from: 60-14
O=C1C=CC[C@H](/C=C/[C@@](C)(O)[C@H](OP(O)(O)=O)C[C@@H](O)/C=C\C=C/C=C/CO)O1
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture