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BGC0001455Hybrid

Antimycin A1B

Producing organism
Streptomyces argillaceus
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I);PKS (Unknown)
Total steps
11
DOI
MIBiG entry
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antimycin A1B
C28H40N2O9548.27 Da

Gene Cluster Map16 genes · 26,743 bp

CACCALKRKSATTEERAKRAmT5 kb26.7 kb visible · 26,743 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Other
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
EREnoylreductase (ER)
KRKetoreductase (KR)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
CALCoA-ligase (CAL)
AmTAminotransferase V

Pathway Graphsteps arranged in biosynthetic order

11 steps · 10 edges
Step 1
Start
Step 2
antaN
Step 3
antaP
Step 4
antaF, antaG
Step 5
antaH, antaI, antaJ, an…
Step 6
?
Step 7M1
antaC
+Threonine
Step 8M2
antaC
+Pyruvate
Step 9M3
antaD, antaE
+Hexylmalonyl-CoA
Step 10TE
antaD
Step 11
antaB, antaO
+?
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions11 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
11455-1Start
N[C@H](C(O)=O)CC1=CNC2=CC=CC=C21
21455-2antaN
1455-1
from: 1455-1
O=C(C[C@H](N)C(O)=O)C1=CC=CC=C1NC=O
31455-3antaP
1455-2
from: 1455-2
OC(C1=C(N)C=CC=C1)=O
41455-4antaF, antaG
1455-3
from: 1455-3
OC(C1=C(N)C=CC=C1)=O
51455-5antaH, antaI, antaJ, antaK, antaL
1455-4
from: 1455-4
OC(C12C(O2)=CC=CC1N)=O
61455-6?
1455-5
from: 1455-5
OC(C1=C(O)C(N)=CC=C1)=O
71455-7antaCM1
1455-6;Threonine
from: 1455-6
O=C(N[C@@H]([C@@H](C)O)C(O)=O)C1=C(O)C(N)=CC=C1
81455-8antaCM2
1455-7;Pyruvate
from: 1455-7
O=C(N[C@@H]([C@@H](C)O)C(O[C@@H](C)C(O)=O)=O)C1=C(O)C(N)=CC=C1
91455-9antaD, antaEM3
1455-8;Hexylmalonyl-CoA
from: 1455-8
O=C(N[C@@H]([C@@H](C)O)C(O[C@@H](C)C([C@@H](CCCCCC)C(O)=O)=O)=O)C1=C(O)C(N)=CC=C1
101455-10antaDTE
1455-9
from: 1455-9
NC1=CC=CC(C(NC([C@@H](C)OC([C@H](CCCCCC)[C@@H](O)[C@H](C)O2)=O)C2=O)=O)=C1O
111455antaB, antaO
1455-10;?
from: 1455-10
OC(C(NC=O)=CC=C1)=C1C(NC([C@@H](C)OC([C@H](CCCCCC)[C@@H](OC(CC(C)C)=O)[C@H](C)O2)=O)C2=O)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture