← Back to Repository
BGC0000319NRPS

cephamycin C

Producing organism
Streptomyces clavuligerus
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I)
Total steps
9
DOI
MIBiG entry
View on MIBiG ↗
Loading…
cephamycin C
C16H22N4O9S446.11 Da

Gene Cluster Map19 genes · 34,452 bp

AmTAmTACACAETE5 kb34.5 kb visible · 34,452 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Resistance
Unknown
Domains
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
TEThioesterase (TE)
EEpimerization (E)
AmTAminotransferase III
AmTAminotransferase V

Pathway Graphsteps arranged in biosynthetic order

9 steps · 8 edges
Step 1M1
SSCG_00146
+L-α-Aminoadipic a…
Step 2M2
SSCG_00146
+L-cysteine
Step 3M3
SSCG_00146
+L-Valine
Step 4
SSCG_00147
Step 5
SSCG_00135
Step 6
SSCG_00134
Step 7
SSCG_00139
Step 8
SSCG_00140
Step 9
SSCG_00137,SSCG_00128
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions9 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1319-1SSCG_00146M1
L-α-Aminoadipic acid
NC(C(O)=O)CCCC(O)=O
2319-2SSCG_00146M2
319-1;L-cysteine
from: 319-1
NC(CCCC(NC(C(O)=O)CS)=O)C(O)=O
3319-3SSCG_00146M3
319-2;L-Valine
from: 319-2
NC(CCCC(NC(C(N[C@@](C)(C(O)=O)C(C)C)=O)CS)=O)C(O)=O
4319-4SSCG_00147
319-3
from: 319-3
NC(CCCC(NC1C2SC(C)(C)[C@](C)(C(O)=O)N2C1=O)=O)C(O)=O
5319-5SSCG_00135
319-4
from: 319-4
NC(CCCC(NC1C2SC(C)(C)[C@](C)(C(O)=O)N2C1=O)=O)C(O)=O
6319-6SSCG_00134
319-5
from: 319-5
NC(CCCC(NC1[C@@H]2N(C(C(O)=O)=C(C)CS2)C1=O)=O)C(O)=O
7319-7SSCG_00139
319-6
from: 319-6
NC(CCCC(NC1[C@@H]2N(C(C(O)=O)=C(CO)CS2)C1=O)=O)C(O)=O
8319-8SSCG_00140
319-7
from: 319-7
NC(CCCC(NC1[C@@H]2N(C(C(O)=O)=C(COC(N)=O)CS2)C1=O)=O)C(O)=O
9319SSCG_00137,SSCG_00128
319-8
from: 319-8
NC(CCCC(N[C@@]1(OC)[C@@H]2N(C(C(O)=O)=C(COC(N)=O)CS2)C1=O)=O)C(O)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture