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BGC0000360NRPS

GE81112

Producing organism
Streptomyces sp. L-49973
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I)
Total steps
12
DOI
MIBiG entry
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GE81112
C24H35ClN10O10658.22 Da

Gene Cluster Map28 genes · 55,651 bp

AACACAACAC10 kb55.6 kb visible · 55,651 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Unknown
Domains
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
ACPAcyl carrier (ACP)
TEThioesterase (TE)
TauDTauD oxygenase

Pathway Graphsteps arranged in biosynthetic order

12 steps · 11 edges
Step 1
start
+(2S)-Lysine
Step 7
Start
+(2S)-Histidine
Step 2
getD
Step 8
getM
Step 12TE
thioesterase
Step 3
getF
Step 9
getL
Step 4M1
getE;getH
Step 10TE
getA
Step 5M2
getH
+(2S)-5-hydroxy-2-…
Step 6M3
getH
+(2S)-Histidine
Step 11M4
getH;getJ;getI
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions12 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1360-1start
(2S)-Lysine
N[C@H](C(O)=O)CCCCN
2360-2getD
360-1
from: 360-1
O=C([C@H]1NCCCC1)O
3360-3getF
360-2
from: 360-2
O[C@@H]1[C@@H](C(O)=O)NCCC1
4360-4getE;getHM1
360-3
from: 360-3
O[C@H]1CCCN[C@H]1C(O)=O
5360-5getHM2
360-4;(2S)-5-hydroxy-2-aminopentanoic acid
from: 360-4
O=C(N[C@H](C(O)=O)C[C@H](CO)O)[C@H]1NCCC[C@@H]1O
6360-6getHM3
360-5;(2S)-Histidine
from: 360-5
O=C(N[C@H](C(N[C@@H](CC1=CN=CN1)C(O)=O)=O)C[C@H](CO)O)[C@H]2NCCC[C@@H]2O
7360-7Start
(2S)-Histidine
O=C(O)[C@@H](N)CC1=CN=CN1
8360-8getM
360-7
from: 360-7
O=C(O)[C@@H](N)CC1=CN=CN1
9360-9getL
360-8
from: 360-8
O=C(O)[C@@H](N)CC1=CN=C(Cl)N1
10360-10getATE
360-9
from: 360-9
O=C(O)[C@@H](N)CC1=CN=C(Cl)N1
11360-11getH;getJ;getIM4
360-6;360-10
from: 360-6, 360-10
O=C(N[C@H](C(N[C@@H](CC1=CN=CN1)C(N[C@H](C(O)=O)[C@@H](C2=CN=C(Cl)N2)O)=O)=O)C[C@H](CO)O)[C@H]3NCCC[C@@H]3O
12360thioesteraseTE
360-7
from: 360-7
O=C(N[C@H](C(N[C@@H](CC1=CN=CN1)C(N[C@H](C(O)=O)[C@@H](C2=CN=C(Cl)N2)O)=O)=O)C[C@H](COC(N)=O)O)[C@H]3NCCC[C@@H]3O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture