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BGC0000289NRPS

A40926 A1

Producing organism
Nonomuraea gerenzanensis
Taxonomy
BacteriaActinomycetotaActinomycetesStreptosporangialesStreptosporangiaceaeNonomuraea
Biosynthetic class
NRPS (Type 1)
Total steps
9
DOI
MIBiG entry
View on MIBiG ↗

Gene Cluster Map55 genes · 89,153 bp

20 kb89.2 kb visible · 89,153 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Other
Unknown
Domains
KRKetoreductase (KR)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
CnCOM N-term
TEThioesterase (TE)
EEpimerization (E)
ECHEnoyl-CoA hydratase
AmTAminotransferase I/II
XPutative domain (X)
TgrTIGR01720

Pathway Graphsteps arranged in biosynthetic order

9 steps · 8 edges
Step 1M1
dbv25
+4-hydroxyphenylgl…
Step 2M2
dbv25
+Tyrosine
Step 3M3
dbv26
+3,5-dihydroxyphen…
Step 4M4
dbv17
+4-hydroxyphenylgl…
Step 5M5
dbv17
+4-hydroxyphenylgl…
Step 6M6
dbv17,dbv28
+Tyrosine
Step 7M7
dbv16
+3,5-dihydroxyphen…
Step 8TE
dbv16
Step 9
dbv8,dbv9,dbv10,dbv20,d…
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions9 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1289-1dbv25M1
4-hydroxyphenylglycine
OC(C(C1=CC=C(O)C=C1)N)=O
2289-2dbv25M2
289-1;Tyrosine
from: 289-1
OC(C(CC1=CC=C(O)C=C1)NC(C(C2=CC=C(O)C=C2)N)=O)=O
3289-3dbv26M3
289-2;3,5-dihydroxyphenylglycine
from: 289-2
OC(C(C1=CC(O)=CC(O)=C1)NC(C(CC2=CC=C(O)C=C2)NC(C(C3=CC=C(O)C=C3)N)=O)=O)=O
4289-4dbv17M4
289-3;4-hydroxyphenylglycine
from: 289-3
OC(C(C1=CC=C(O)C=C1)NC(C(C2=CC(O)=CC(O)=C2)NC(C(CC3=CC=C(O)C=C3)NC(C(C4=CC=C(O)C=C4)N)=O)=O)=O)=O
5289-5dbv17M5
289-4;4-hydroxyphenylglycine
from: 289-4
OC(C(NC(C(C1=CC=C(O)C=C1)NC(C(C2=CC(O)=CC(O)=C2)NC(C(CC3=CC=C(O)C=C3)NC(C(C4=CC=C(O)C=C4)N)=O)=O)=O)=O)C5=CC=C(O)C=C5)=O
6289-6dbv17,dbv28M6
289-5;Tyrosine
from: 289-5
OC(C(NC(C(NC(C(C1=CC=C(O)C=C1)NC(C(C2=CC(O)=CC(O)=C2)NC(C(CC3=CC=C(O)C=C3)NC(C(C4=CC=C(O)C=C4)N)=O)=O)=O)=O)C5=CC=C(O)C=C5)=O)C(C6=CC=C(O)C=C6)O)=O
7289-7dbv16M7
289-6;3,5-dihydroxyphenylglycine
from: 289-6
OC(C(NC(C(NC(C(NC(C(C1=CC=C(O)C=C1)NC(C(C2=CC(O)=CC(O)=C2)NC(C(CC3=CC=C(O)C=C3)NC(C(C4=CC=C(O)C=C4)N)=O)=O)=O)=O)C5=CC=C(O)C=C5)=O)C(C6=CC=C(O)C=C6)O)=O)C7=CC(O)=CC(O)=C7)=O
8289-8dbv16TE
289-7
from: 289-7
O=C([C@@H](C1=CC2=C(O)C3=C1)NC[C@@H](NC([C@@H](CC4=CC=C(O2)C=C4)NC([C@H](N)C5=CC6=C(O)C=C5)=O)=O)C7=C(Cl)C(O)=CC(O6)=C7)N[C@@H](C(N[C@@H]([C@@H](C8=CC=C(O3)C(Cl)=C8)O)C(N[C@@H](C(O)=O)C9=CC(O)=CC(O)=C9%10)=O)=O)C%11=CC=C(O)C%10=C%11
9289dbv8,dbv9,dbv10,dbv20,dbv21,dbv23,dbv27,dbv29
2344-8
from: 2344-8
O=C([C@@H](C1=CC2=C(O[C@H]3O[C@@H](C(O)=O)[C@H](O)C(O)[C@@H]3NC(CCCCCCCC(C)C)=O)C4=C1)NC[C@@H](NC([C@@H](CC5=CC=C(O2)C=C5)NC([C@H](NC)C6=CC7=C(O)C=C6)=O)=O)C8=C(Cl)C(O)=CC(O7)=C8)N[C@@H](C(N[C@@H]([C@@H](C9=CC=C(O4)C(Cl)=C9)O)C(N[C@@H](C(O)=O)C%10=CC(O)=CC(O[C@@H]%11[C@@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O%11)=C%10%12)=O)=O)C%13=CC=C(O)C%12=C%13
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture