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BGC0002014Hybrid

pepticinnamin E

Producing organism
Actinobacteria bacterium OK006
Taxonomy
BacteriaActinobacteria
Biosynthetic class
NRPS(Type1), PKS (unknown)
Total steps
8
DOI
MIBiG entry
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pepticinnamin E
C49H54ClN5O10907.36 Da

Gene Cluster Map31 genes · 44,694 bp

CACAMTKSKSKSCAMTCACATE10 kb44.7 kb visible · 44,694 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
KSKetosynthase (KS)
KRKetoreductase (KR)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
MTMethyltransferase

Pathway Graphsteps arranged in biosynthetic order

8 steps · 7 edges
Step 1
start
+?
Step 2M1
OK006_RS36465
+D-Tyrosine
Step 3M2
OK006_RS36465
+L-Tyrosine
Step 4
OK006_RS36460,OK006_RS3…
Step 5M3
OK006_RS36605
+L-Phenylalanine
Step 6M4
OK006_RS36605
+D-Serine
Step 7M5
OK006_RS36605
+Glycine
Step 8TE
OK006_RS36605
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions8 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
12014-1start
?
OC(/C=C/C1=C(/C=C\CCC)C=CC=C1)=O
22014-2OK006_RS36465M1
2014-1;D-Tyrosine
from: 2014-1
NC([C@@H](CC1=CC=C(O)C=C1)NC(/C=C/C2=C(/C=C\CCC)C=CC=C2)=O)=O
32014-3OK006_RS36465M2
2014-2;L-Tyrosine
from: 2014-2
NC([C@H](CC1=CC=C(O)C=C1)N(C)C([C@@H](CC2=CC=C(O)C=C2)NC(/C=C/C3=C(/C=C\CCC)C=CC=C3)=O)=O)=O
42014-4OK006_RS36460,OK006_RS36505,OK006_RS36510
2014-3
from: 2014-3
NC([C@H](CC1=CC=C(OC)C(O)=C1Cl)N(C)C([C@@H](CC2=CC=C(O)C=C2)NC(/C=C/C3=C(/C=C\CCC)C=CC=C3)=O)=O)=O
52014-5OK006_RS36605M3
2014-4;L-Phenylalanine
from: 2014-4
OC([C@H](CC1=CC=CC=C1)N(C([C@H](CC2=CC=C(OC)C(O)=C2Cl)N(C)C([C@@H](CC3=CC=C(O)C=C3)NC(/C=C/C4=C(/C=C\CCC)C=CC=C4)=O)=O)=O)C)=O
62014-6OK006_RS36605M4
2014-5;D-Serine
from: 2014-5
NC([C@H](N)COC([C@H](CC1=CC=CC=C1)N(C([C@H](CC2=CC=C(OC)C(O)=C2Cl)N(C)C([C@@H](CC3=CC=C(O)C=C3)NC(/C=C/C4=C(/C=C\CCC)C=CC=C4)=O)=O)=O)C)=O)=O
72014-7OK006_RS36605M5
2014-6;Glycine
from: 2014-6
O=C(O)CNC([C@H](N)COC([C@H](CC1=CC=CC=C1)N(C([C@H](CC2=CC=C(OC)C(O)=C2Cl)N(C)C([C@@H](CC3=CC=C(O)C=C3)NC(/C=C/C4=C(/C=C\CCC)C=CC=C4)=O)=O)=O)C)=O)=O
82014OK006_RS36605TE
2014-7
from: 2014-7
O=C([C@H](N1)COC([C@H](CC2=CC=CC=C2)N(C([C@H](CC3=CC=C(OC)C(O)=C3Cl)N(C)C([C@@H](CC4=CC=C(O)C=C4)NC(/C=C/C5=C(/C=C\CCC)C=CC=C5)=O)=O)=O)C)=O)NCC1=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture