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BGC0000366NRPS

gobichelin A;gobichelin B

Producing organism
Streptomyces sp. NRRL F-4415
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I)
Total steps
9
DOI
MIBiG entry
View on MIBiG ↗
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C30H41N9O9671.30 Da

Gene Cluster Map18 genes · 36,842 bp

CyAACACAECACATE5 kb36.8 kb visible · 36,842 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
CnCOM N-term
CcCOM C-term
TEThioesterase (TE)
EEpimerization (E)
CyHeterocyclization (Cy)
TgrTIGR01720

Pathway Graphsteps arranged in biosynthetic order

9 steps · 8 edges
Step 1
start
+Chorismic acid
Step 2Load
gobH
Step 3M1
gobJ
+Serine
Step 4M2
gobR
+Histidine
Step 5M3
gobR
+Lysine
Step 6M4
gobS
+Serine
Step 7M5
gobS
+N-hydroxyl-ornith…
Step 8TE
gobS
Step 9TE
gobS
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions9 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1366-1start
Chorismic acid
O[C@@H]1C=CC(C(O)=O)=C[C@H]1OC(C(O)=O)=C
2366-2gobHLoading
366-1
from: 366-1
O=C(O)C1=C(O)C=CC=C1
3366-3gobJM1
366-2;Serine
from: 366-2
OC([C@H]1N=C(OC1)C2=C(O)C=CC=C2)=O
4366-4gobRM2
366-3;Histidine
from: 366-3
O=C(O)[C@H](CC1=CN=CN1)NC([C@H]2N=C(OC2)C3=C(O)C=CC=C3)=O
5366-5gobRM3
366-4;Lysine
from: 366-4
O=C(NC(C(O)=O)CCCCN)[C@H](CC1=CN=CN1)NC([C@H]2N=C(OC2)C3=C(O)C=CC=C3)=O
6366-6gobSM4
366-5;Serine
from: 366-5
O=C(NC(C(N[C@@H](CO)C(O)=O)=O)CCCCN)[C@H](CC1=CN=CN1)NC([C@H]2N=C(OC2)C3=C(O)C=CC=C3)=O
7366-7gobSM5
366-6;N-hydroxyl-ornithine
from: 366-6
O=C(NC(C(N[C@@H](CO)C(N[C@@H](C(O)=O)CCCNO)=O)=O)CCCCN)[C@H](CC1=CN=CN1)NC([C@H]2N=C(OC2)C3=C(O)C=CC=C3)=O
8366(1)gobSTE
366-7
from: 366-7
O=C(NC(C(N[C@@H](CO)C(N[C@H]1CCCN(O)C1=O)=O)=O)CCCCN)[C@H](CC2=CN=CN2)NC([C@H]3N=C(OC3)C4=C(O)C=CC=C4)=O
9366(2)gobSTE
366-7
from: 366-7
O=C(NC(C(N[C@@H](CO)C(N[C@H]1CCCN(O)C1=O)=O)=O)CCCCN)[C@H](CC2=CN=CN2)NC([C@H](CO)NC(C3=C(O)C=CC=C3)=O)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture