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BGC0001213PKS

Nataxazole

Producing organism
Streptomyces sp. Tu 6176
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
PKS (Unknown)
Total steps
20
DOI
MIBiG entry
View on MIBiG ↗
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nataxazole
C23H16N2O5400.11 Da

Gene Cluster Map27 genes · 45,517 bp

AmTTDAKSATKSAT10 kb45.5 kb visible · 45,517 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
KRKetoreductase (KR)
ACPAcyl carrier protein (ACP)
ACPAcyl carrier (ACP)
AAdenylation (A)
ACPAcyl carrier (ACP)
CycPolyketide cyclase
TDTerminal reductase
ACPSACP synthase
AmTAminotransferase III

Pathway Graphsteps arranged in biosynthetic order

20 steps · 20 edges
Step 1
CF54_07385
Iterative
Step 5
Start
Step 2
?
Step 6
CF54_07335
Step 3
CF54_07370
Step 7
?
Step 4
CF54_07375;CF54_07365
Step 8
CF54_07345
Step 9
CF54_07350
Step 10
CF54_07355
Step 11
CF54_07380
Step 12
CF54_07375;CF54_07410
Step 13
?
Step 14
?
Step 15
?
Step 16
?
Step 17
?
Step 18
?
Step 19
CF54_07360
Step 20
?
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions20 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
11213-1CF54_07385
OC(CC(CC(O)CC(C)=O)=O)=O{'Iteration': [([None], 'Ace…
21213-2?
1213-1
from: 1213-1
OC(C1=C(C)C=CC=C1O)=O
31213-3CF54_07370
1213-2
from: 1213-2
[R]C(C1=C(C)C=CC=C1O)=O
41213-4CF54_07375;CF54_07365
1213-3
from: 1213-3
OC(C1=C(C)C=CC=C1O)=O
51213-5Start
[H][C@]([C@](O)(CO[R])[H])(O)C([H])=O
61213-6CF54_07335
1213-5
from: 1213-5
[H][C@]([C@](O)(CO[R])[H])(O)[C@@](O)(C)CC(C(O)=O)=O
71213-7?
1213-6
from: 1213-6
O[C@@H]1C=CC(C(O)=O)=C[C@H]1OC(C(O)=O)=C
81213-8CF54_07345
1213-7
from: 1213-7
C=C(C(O)=O)O[C@H]([C@H]1N)C=CC=C1C(O)=O
91213-9CF54_07350
1213-8
from: 1213-8
O[C@H]([C@H]1N)C=CC=C1C(O)=O
101213-10CF54_07355
1213-9
from: 1213-9
OC1=C(N)C(C(O)=O)=CC=C1
111213-11CF54_07380
1213-10
from: 1213-10
OC1=C(N)C(C([R])=O)=CC=C1
121213-12CF54_07375;CF54_07410
1213-11
from: 1213-11
OC1=C(N)C(C(O)=O)=CC=C1
131213-13?
1213-4;1213-12
from: 1213-4, 1213-12
O=C(NC1=C(O)C=CC=C1C(O)=O)C2=C(C)C=CC=C2O
141213-14?
1213-13
from: 1213-13
OC(C1=CC=CC(O2)=C1NC2(O)C3=C(C)C=CC=C3O)=O
151213-15?
1213-14
from: 1213-14
OC(C1=CC=CC(O2)=C1N=C2C3=C(C)C=CC=C3O)=O
161213-16?
1213-12;1213-15
from: 1213-12, 1213-15
O=C(NC1=C(O)C=CC=C1C(O)=O)C2=CC=CC(O3)=C2N=C3C4=C(C)C=CC=C4O
171213-17?
1213-16
from: 1213-16
OC1=CC=CC(C)=C1C2=NC3=C(O2)C=CC=C3C(O4)(O)NC5=C4C=CC=C5C(O)=O
181213-18?
1213-17
from: 1213-17
OC1=CC=CC(C)=C1C2=NC3=C(O2)C=CC=C3C(O4)=NC5=C4C=CC=C5C(O)=O
191213-19CF54_07360
1213-18
from: 1213-18
OC1=CC=CC(C)=C1C2=NC3=C(O2)C=CC=C3C(O4)=NC5=C4C=CC=C5C(O)=O
201213?
1213-19
from: 1213-19
OC1=CC=CC(C)=C1C2=NC3=C(O2)C=CC=C3C(O4)=NC5=C4C=CC=C5C(O)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture