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BGC0001027Hybrid

Nocobactin NA;Nocobactin NA 10152B

Producing organism
Nocardia farcinica IFM 10152
Taxonomy
BacteriaActinomycetotaActinomycetesMycobacterialesNocardiaceaeNocardia
Biosynthetic class
NRPS (Type I);PKS (Unknown)
Total steps
10
DOI
MIBiG entry
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C36H53N5O10715.38 Da

Gene Cluster Map8 genes · 20,510 bp

TEKSATKRCACCAECyA5 kb20.5 kb visible · 20,510 bp total
Biosynthetic (core)
Biosynthetic (additional)
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
KRKetoreductase (KR)
ACPAcyl carrier (ACP)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
EEpimerization (E)
CyHeterocyclization (Cy)

Pathway Graphsteps arranged in biosynthetic order

10 steps · 9 edges
Step 1
Start
+Chorismate
Step 2
?
Step 3
?
Step 4
nbtF
+Threonine
Step 5
nbtD
+Lysine
Step 6
nbtB;nbtC, nbtD
+(Caoryl-CoA/Laury…
Step 7
nbtH
+Malonyl-CoA
Step 8
nbtE
+Lysine
Step 9(1)
mbtG, nbtE
Step 9(2)
mbtG, nbtE
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions10 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
11027-1Start
Chorismate
OC1C=CC(C(O)=O)=CC1OC(C(O)=O)=C
21027-2?
1027-1
from: 1027-1
OC(C1=CC=CC=C1O)=O
31027-3?
1027-2
from: 1027-2
[R]C(C1=CC=CC=C1O)=O
41027-4nbtF
1027-3;Threonine
from: 1027-3
OC1=C(C2=NC(C(O)=O)=C(C)O2)C=CC=C1
51027-5nbtD
1027-4;Lysine
from: 1027-4
OC1=C(C2=NC(C(NC(CCCCN)C(O)=O)=O)=C(C)O2)C=CC=C1
61027-6nbtB;nbtC, nbtD
1027-5;(Caoryl-CoA/Lauryl-CoA)
from: 1027-5
OC1=C(C2=NC(C(NC(CCCCN)C(OC([R])C(C(O)=O)C)=O)=O)=C(C)O2)C=CC=C1
71027-7nbtH
1027-6;Malonyl-CoA
from: 1027-6
OC1=C(C2=NC(C(NC(CCCCNC(C)=O)C(OC([R])C(C(O)=O)C)=O)=O)=C(C)O2)C=CC=C1
81027-8nbtE
1027-7;Lysine
from: 1027-7
OC1=C(C2=NC(C(NC(CCCCNC(C)=O)C(OC([R])C(C(N[C@H](CCCCN)C(O)=O)=O)C)=O)=O)=C(C)O2)C=CC=C1
9(1)1027(1)mbtG, nbtE
1027-8
from: 1027-8
OC1=C(C2=NC(C(NC(CCCCNC(C)=O)C(OC(CCCCCCC)C(C(N[C@@H]3CCCCN(O)C3=O)=O)C)=O)=O)=C(C)O2)C=CC=C1
9(2)1027(2)mbtG, nbtE
1027-8
from: 1027-8
OC1=C(C2=NC(C(NC(CCCCNC(C)=O)C(OC(CCCCCCCCC)C(C(N[C@@H]3CCCCN(O)C3=O)=O)C)=O)=O)=C(C)O2)C=CC=C1
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture