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BGC0001801NRPS

Thiazostatin;Watasemycin A;Watasemycin B;2-hydroxyphenylthiazoline enantiopyochelin;Isopyochelin

Producing organism
Streptomyces venezuelae ATCC 10712
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I)
Total steps
11
DOI
MIBiG entry
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C16H20N2O3S2352.09 Da

Gene Cluster Map15 genes · 28,811 bp

AATECyACyAMTTE5 kb28.8 kb visible · 28,811 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
CyHeterocyclization (Cy)
MTMethyltransferase

Pathway Graphsteps arranged in biosynthetic order

11 steps · 10 edges
Step 1
Start
Step 2
SVEN_0516
Step 3
SVEN_0510;SVEN_0512
Step 4
SVEN_0512
+Cysteine
Step 5
SVEN_0517
+Cysteine
Step 6
SVEN_0516
Step 7
SVEN_0517
Step 11TE
SVEN_0517
Step 8TE
SVEN_0517
Step 9
SVEN_0515
+1801(1)
Step 10
SVEN_0515
+1801(1)
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions11 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
11801-1Start
OC(C1=CC(OC(C(O)=O)=C)[C@H](O)C=C1)=O
21801-2SVEN_0516
1801-1
from: 1801-1
OC(C1=CC=CC=C1O)=O
31801-3SVEN_0510;SVEN_0512
1801-2
from: 1801-2
OC(C1=CC=CC=C1O)=O
41801-4SVEN_0512
1801-3;Cysteine
from: 1801-3
OC([C@@]1([H])N=C(C2=C(O)C=CC=C2)SC1)=O
51801-5SVEN_0517
1801-4;Cysteine
from: 1801-4
[H][C@]1(C2=N[C@](C(O)=O)(C)CS2)N=C(C3=C(O)C=CC=C3)SC1
61801-6SVEN_0516
1801-5
from: 1801-5
[H][C@]1(C2([H])SC[C@@](C(O)=O)(C)N2)N=C(C3=C(O)C=CC=C3)SC1
71801-7SVEN_0517
1801-6
from: 1801-6
[H][C@]1(C2([H])SC[C@@](C(O)=O)(C)N2C)N=C(C3=C(O)C=CC=C3)SC1
81801(1)SVEN_0517TE
1801-7
from: 1801-7
[H][C@]1(C2([H])SC[C@@](C(O)=O)(C)N2C)N=C(C3=C(O)C=CC=C3)SC1
91801(2)SVEN_0515
1801(1)
OC(C=CC=C1)=C1C2=N[C@]([C@]3([H])SC[C@](C)(C(O)=O)N3C)([H])[C@@](C)([H])S2
101801(3)SVEN_0515
1801(1)
OC(C=CC=C1)=C1C2=N[C@@]([C@@]3([H])SC[C@](C)(C(O)=O)N3C)([H])[C@@](C)([H])S2
111801(4)SVEN_0517TE
1801-6
from: 1801-6
[H][C@]1(C2([H])SC[C@@](C(O)=O)(C)N2)N=C(C3=C(O)C=CC=C3)SC1
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture