← Back to Repository
BGC0000973Hybrid

Collismycin A

Producing organism
Streptomyces sp. CS40
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I);PKS (Type I)
Total steps
17
DOI
MIBiG entry
View on MIBiG ↗
Loading…
collismycin A
C13H13N3O2S275.07 Da

Gene Cluster Map27 genes · 46,672 bp

AmTAAKSATCyACATEAMT10 kb46.7 kb visible · 46,672 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
CnCOM N-term
CcCOM C-term
TEThioesterase (TE)
CyHeterocyclization (Cy)
MTMethyltransferase
AmTAminotransferase III

Pathway Graphsteps arranged in biosynthetic order

17 steps · 16 edges
Step 1
Start
Step 2
clmL
Step 3
?
Step 4
clmS
Step 5
clmAL
Step 6
clmP, clmN1
Step 7
clmN1
+Malonyl-CoA
Step 8
?
Step 9
?
Step 10
clmN1
+Cysteine, CoA?
Step 11
clmN2
+Leucine
Step 12
clmT, clmD1?, clmD2?, c…
Step 13
clmM1
Step 14
clmAH
Step 15
clmG1, clmG2
Step 16
clmAT
Step 17
clmM2
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions17 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1973-1Start
N[C@H](C(O)=O)CCCCN
2973-2clmL
973-1
from: 973-1
NCCCCC(C(O)=O)=O
3973-3?
973-2
from: 973-2
OC(C1=NCCCC1)=O
4973-4clmS
973-3
from: 973-3
OC(C1=NC=CC=C1)=O
5973-5clmAL
973-4
from: 973-4
[R]C(C1=NC=CC=C1)=O
6973-6clmP, clmN1
973-5
from: 973-5
OC(C1=NC=CC=C1)=O
7973-7clmN1
973-6;Malonyl-CoA
from: 973-6
O=C(CC(O)=O)C1=NC=CC=C1
8973-8?
973-7
from: 973-7
OC(CC(O)=O)C1=NC=CC=C1
9973-9?
973-8
from: 973-8
O=C(O)/C=C/C1=NC=CC=C1
10973-10clmN1
973-9;Cysteine, CoA?
from: 973-9
O=C([R])/C=C(NC(CS)C(O)=O)/C1=NC=CC=C1
11973-11clmN2
973-10;Leucine
from: 973-10
O=C([R])/C=C(NC(CS)C(NC(C(O)=O)CC(C)C)=O)/C1=NC=CC=C1
12973-12clmT, clmD1?, clmD2?, clmM?, ?
973-11
from: 973-11
O=C1C2=NC(C3=NC=CC=C3)=CC(O)=C2SN1C(C(O)=O)CC(C)C
13973-13clmM1
973-12
from: 973-12
O=C(NC(C(O)=O)CC(C)C)C1=NC(C2=NC=CC=C2)=CC(O)=C1SC
14973-14clmAH
973-13
from: 973-13
OC(C1=NC(C2=NC=CC=C2)=CC(O)=C1SC)=O
15973-15clmG1, clmG2
973-14
from: 973-14
[H]C(C1=NC(C2=NC=CC=C2)=CC(O)=C1SC)=O
16973-16clmAT
973-15
from: 973-15
OC1=C(SC)C(/C=N/O)=NC(C2=NC=CC=C2)=C1
17973clmM2
973-16
from: 973-16
CSC1=C(OC)C=C(N=C1/C=N/O)C2=NC=CC=C2
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture