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BGC0002448NRPS

Q6402A

Producing organism
Streptomyces violaceusniger
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomycesStreptomyces violaceusniger group
Biosynthetic class
NRPS (Type I)
Total steps
12
DOI
MIBiG entry
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Q6402A
C50H61N7O12951.44 Da

Gene Cluster Map40 genes · 59,505 bp

CACACACACAECAAmTAmT10 kb59.5 kb visible · 59,505 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Other
Unknown
Domains
EREnoylreductase (ER)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
CnCOM N-term
TEThioesterase (TE)
EEpimerization (E)
MTMethyltransferase
AmTAminotransferase I/II
TgrTIGR01720

Pathway Graphsteps arranged in biosynthetic order

12 steps · 11 edges
Step 1
Start
+Isopentylmalonyl-…
Step 7
Start
+SAM
Step 2M1
orf22
+Threonine
Step 8
orf29
Step 9
orf29
Step 3M2
orf22
+Phenylalanine
Step 10
orf30
Step 4M3
orf22
+Asparagine
Step 5M4
orf22
+Tryptophan
Step 6M5
orf22
+4-Hydroxyphenylgl…
Step 11M6
orf23
Step 12TE
orf23
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions12 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
12448-1Start
Isopentylmalonyl-CoA
CC(C)CCCC(O)=O
22448-2orf22M1
2448-1;Threonine
from: 2448-1
OC(C(C(O)C)NC(CCCC(C)C)=O)=O
32448-3orf22M2
2448-2;Phenylalanine
from: 2448-2
O=C(C(N(C(C(C(O)C)NC(CCCC(C)C)=O)=O)C)CC1=CC=CC=C1)O
42448-4orf22M3
2448-3;Asparagine
from: 2448-3
O=C(C(N(C(C(C(O)C)NC(CCCC(C)C)=O)=O)C)CC1=CC=CC=C1)NC(C(O)=O)CCC(O)=O
52448-5orf22M4
2448-4;Tryptophan
from: 2448-4
O=C(C(N(C(C(C(O)C)NC(CCCC(C)C)=O)=O)C)CC1=CC=CC=C1)NC(C(NC(C(O)=O)CC2=CNC3=C2C=C(C=C3)O)=O)CCC(O)=O
62448-6orf22M5
2448-5;4-Hydroxyphenylglycine
from: 2448-5
O=C(C(N(C(C(C(O)C)NC(CCCC(C)C)=O)=O)C)CC1=CC=CC=C1)NC(C(NC(C(NC(C(O)=O)C2=CC=C(C=C2)O)=O)CC3=CNC4=C3C=C(C=C4)O)=O)CCC(O)=O
72448-7Start
SAM
N[C@@](C(O)=O)([H])CC[S+](C)[Ado]
82448-8orf29
2448-7
from: 2448-7
N[C@@](C(O)=O)([H])CC(C)[S+](C)[Ado]
92448-9orf29
2448-7
from: 2448-7
N[C@@](C(O)=O)([H])C(C)C[S+](C)[Ado]
102448-10orf30
2448-8/2448-9
from: 2448-8/2448-9
NC1(C[C@@H]1C)C(O)=O
112448-11orf23M6
2448-6;2448-10
from: 2448-6, 2448-10
O=C(C(N(C(C(C(O)C)NC(CCCC(C)C)=O)=O)C)CC1=CC=CC=C1)NC(C(NC(C(NC(C(NC2(C(C2)C)C(O)=O)=O)C3=CC=C(C=C3)O)=O)CC4=CNC5=C4C=C(C=C5)O)=O)CCC(O)=O
122448orf23TE
2448-11
from: 2448-11
O=C(NC(CCC(O)=O)C(NC(CC1=CNC2=C1C=C(O)C=C2)C(NC(C3=CC=C(O)C=C3)C(NC4(C(C)C4)C(OC(C)C5NC(CCCC(C)C)=O)=O)=O)=O)=O)C(CC6=CC=CC=C6)N(C)C5=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture