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BGC0000118PKS

pactamycin

Producing organism
Streptomyces pactum
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Unknown)
Total steps
18
DOI
MIBiG entry
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pactamycin
C28H38N4O8558.27 Da

Gene Cluster Map28 genes · 42,898 bp

KSKSATAAmT10 kb42.9 kb visible · 42,898 bp total
Biosynthetic (core)
Biosynthetic (additional)
Other
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
KRKetoreductase (KR)
ACPAcyl carrier (ACP)
AAdenylation (A)
ACPAcyl carrier (ACP)
AmTAminotransferase III

Pathway Graphsteps arranged in biosynthetic order

18 steps · 17 edges
Step 1
Start
+3-Dehydroshikimate
Step 5
Start
+N-acetylglucosami…
Step 17
pctK;pctS;pctT
Iterative
Step 2
pctC
Step 6
pctL
Step 3
pctU
Step 4
pctQ
Step 7
pctI
Step 8
pctE/pctP
Step 9
pctE/pctP
Step 10
pctV
Step 11
pctJ/pctN/pctO
Step 12
pctJ/pctN/pctO
Step 13
pctJ/pctN/pctO
Step 14
pctA;pctB
Step 15
pctD
Step 16
pctF
Step 18
pctM
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions18 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1118-1Start
3-Dehydroshikimate
O=C1C=C(C(O)=O)C[C@@H](O)[C@@H]1O
2118-2pctC
118-1
from: 118-1
NC1=CC=CC(C(O)=O)=C1
3118-3pctU
118-2
from: 118-2
NC1=CC(C(CC([R])=O)=O)=CC=C1
4118-4pctQ
118-3
from: 118-3
NC1=CC(C(C)=O)=CC=C1
5118-5Start
N-acetylglucosamine
O[C@H]1[C@H](O)[C@@H](NC(C)=O)[C@@H]([R])O[C@@H]1CO
6118-6pctL
118-5
from: 118-5
O[C@H]1[C@H](O)[C@@H](NC(C)=O)[C@H](NC2=CC=CC(C(C)=O)=C2)O[C@@H]1CO
7118-7pctI
118-4;118-6
from: 118-4, 118-6
O[C@H]1[C@H](O)[C@@H](N)[C@H](NC2=CC=CC(C(C)=O)=C2)O[C@@H]1CO
8118-8pctE/pctP
118-7
from: 118-7
O[C@@H]1[C@@H](N)[C@H](NC2=CC=CC(C(C)=O)=C2)[C@](O)(CO)C1=O
9118-9pctE/pctP
118-8
from: 118-8
O=C1[C@@H](N)[C@H](NC2=CC=CC(C(C)=O)=C2)[C@](O)(CO)[C@@H]1O
10118-10pctV
118-9
from: 118-9
N[C@@H]1[C@H](N)[C@@H](O)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
11118-11pctJ/pctN/pctO
118-10
from: 118-10
N[C@@H]1[C@H](N)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
12118-12pctJ/pctN/pctO
118-11
from: 118-11
N[C@@H]1[C@@](N)(C)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
13118-13pctJ/pctN/pctO
118-12
from: 118-12
N[C@@H]1[C@@](N)(CC)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
14118-14pctA;pctB
118-13
from: 118-13
N[C@@H]1[C@@](N)([C@@H](O)C)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
15118-15pctD
118-14
from: 118-14
N[C@@H]1[C@@](NC(N)=O)([C@@H](O)C)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
16118-16pctF
118-15
from: 118-15
N[C@@H]1[C@@](NC(NC)=O)([C@@H](O)C)[C@](O)(C)[C@@](O)(CO)[C@H]1NC2=CC=CC(C(C)=O)=C2
17118-17pctK;pctS;pctT
CC1=C(C(O)=O)C(O)=CC=C1{'Iteration': [(['None'], 'A…
18118pctM
118-16;118-17
from: 118-16, 118-17
N[C@@H]1[C@@](NC(NC)=O)([C@@H](O)C)[C@](O)(C)[C@@](O)(COC(C2=C(C)C=CC=C2O)=O)[C@H]1NC3=CC=CC(C(C)=O)=C3
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture