← Back to Repository
BGC0000966Hybrid

Caerulomycin A

Producing organism
Actinoalloteichus sp. WH1-2216-6
Taxonomy
BacteriaActinomycetotaActinomycetesPseudonocardialesPseudonocardiaceaeActinoalloteichus
Biosynthetic class
NRPS (Type I);PKS (Unknown)
Total steps
13
DOI
MIBiG entry
View on MIBiG ↗
Loading…
caerulomycin A
C12H11N3O2229.09 Da

Gene Cluster Map25 genes · 44,640 bp

AmTAAKSATCyACATEA10 kb44.6 kb visible · 44,640 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Other
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
CnCOM N-term
TEThioesterase (TE)
CyHeterocyclization (Cy)
AmTAminotransferase III
AmTAminotransferase V

Pathway Graphsteps arranged in biosynthetic order

13 steps · 12 edges
Step 1
Start
+L-lysine
Step 2
AFD30956.1
Step 3
AFD30955.1
Step 4Load
AFD30957.1
Step 5M1
AFD30954.1
+Malonyl-CoA
Step 6M2
AFD30954.1
+Serine
Step 7M3
AFD30953.1
+Leucine
Step 8TE
AFD30951.1
Step 9
AFD30949.1
Step 10
AFD30948.1/AFD30947.1
Step 11
AFD30959.1
Step 12
AFD30961.1
Step 13
AFD30960.1
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions13 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1966-1Start
L-lysine
NC(CCCC[NH3+])C(O)=O
2966-2AFD30956.1
966-1
from: 966-1
OC(C1=NCCCC1)=O
3966-3AFD30955.1
966-2
from: 966-2
OC(C1=NC=CC=C1)=O
4966-4AFD30957.1Loading
966-3
from: 966-3
O=C(O)C1=NC=CC=C1
5966-5AFD30954.1M1
966-4;Malonyl-CoA
from: 966-4
O=C(CC(O)=O)C1=NC=CC=C1
6966-6AFD30954.1M2
966-5;Serine
from: 966-5
OC1=CC(C2=NC=CC=C2)=NC(C(O)=O)=C1
7966-7AFD30953.1M3
966-6;Leucine
from: 966-6
OC1=CC(C2=NC=CC=C2)=NC(C(N[C@H](C(O)=O)CC(C)C)=O)=C1
8966-8AFD30951.1TE
966-7
from: 966-7
OC1=CC(C2=NC=CC=C2)=NC(C(N[C@H](C(O)=O)CC(C)C)=O)=C1
9966-9AFD30949.1
966-8
from: 966-8
OC1=CC(C2=NC=CC=C2)=NC(C(O)=O)=C1
10966-10AFD30948.1/AFD30947.1
966-9
from: 966-9
OC1=CC(C2=NC=CC=C2)=NC(C([H])=O)=C1
11966-11AFD30959.1
966-10
from: 966-10
OC1=CC(C2=NC=CC=C2)=NC(CN)=C1
12966-12AFD30961.1
966-11
from: 966-11
OC1=CC(C2=NC=CC=C2)=NC(C=NO)=C1
13966AFD30960.1
966-12
from: 966-12
ON=CC1=CC(OC)=CC(C2=NC=CC=C2)=N1
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture