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BGC0000166PKS

Tylactone

Producing organism
Streptomyces fradiae
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Unknown)
Total steps
9
DOI
MIBiG entry
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tylactone
C23H38O5394.27 Da

Gene Cluster Map7 genes · 43,280 bp

KSATKSATKSATKSATKSATKSATERKSATKSATTE10 kb43.3 kb visible · 43,280 bp total
Biosynthetic (core)
Biosynthetic (additional)
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)

Pathway Graphsteps arranged in biosynthetic order

9 steps · 8 edges
Step 1Load
tylG
+Methylmalonyl-CoA
Step 2M1
tylG
+Methylmalonyl-CoA
Step 3M2
tylG
+Methylmalonyl-CoA
Step 4M3
tylG_rename1
+Malonyl-CoA
Step 5M4
tylG_rename2
+Methylmalonyl-CoA
Step 6M5
tylG_rename2
+Ethylmalonyl-CoA
Step 7M6
tylG_rename3
+Methylmalonyl-CoA
Step 8M7
tylG_rename4
+Malonyl-CoA
Step 9TE
tylG_rename4
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions9 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1166-1tylGLoading
Methylmalonyl-CoA
O=C(CC)O
2166-2tylGM1
166-1;Methylmalonyl-CoA
from: 166-1
O[C@H](CC)[C@@H](C)C(O)=O
3166-3tylGM2
166-2;Methylmalonyl-CoA
from: 166-2
O[C@H](CC)[C@@H](C)/C=C(C)/C(O)=O
4166-4tylG_rename1M3
166-3;Malonyl-CoA
from: 166-3
O[C@H](CC)[C@@H](C)/C=C(C)/C=C/C(O)=O
5166-5tylG_rename2M4
166-4;Methylmalonyl-CoA
from: 166-4
O[C@H](CC)[C@@H](C)/C=C(C)/C=C/C([C@@H](C(O)=O)C)=O
6166-6tylG_rename2M5
166-5;Ethylmalonyl-CoA
from: 166-5
O[C@H](CC)[C@@H](C)/C=C(C)/C=C/C([C@@H](C[C@@H](C(O)=O)CC)C)=O
7166-7tylG_rename3M6
166-6;Methylmalonyl-CoA
from: 166-6
O[C@H](CC)[C@@H](C)/C=C(C)/C=C/C([C@@H](C[C@@H]([C@H](O)[C@H](C(O)=O)C)CC)C)=O
8166-8tylG_rename4M7
166-7;Malonyl-CoA
from: 166-7
O[C@H](CC)[C@@H](C)/C=C(C)/C=C/C([C@@H](C[C@@H]([C@H](O)[C@H]([C@H](O)CC(O)=O)C)CC)C)=O
9166tylG_rename4TE
166-8
from: 166-8
O=C(/C=C/C(C)=C/C(C)[C@@H](CC)O1)[C@H](C)C[C@H](CC)[C@H](O)[C@@H](C)[C@H](O)CC1=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture