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BGC0000365NRPS

glycopeptidolipid

Producing organism
Mycolicibacterium smegmatis MC2 155
Taxonomy
BacteriaActinomycetotaActinomycetesMycobacterialesMycobacteriaceaeMycolicibacterium
Biosynthetic class
NRPS (Type I)
Total steps
10
DOI
MIBiG entry
View on MIBiG ↗

Gene Cluster Map30 genes · 67,229 bp

AAAAKSKSCAL10 kb67.2 kb visible · 67,229 bp total
Biosynthetic (core)
Biosynthetic (additional)
Transport
Other
Unknown
Domains
KSKetosynthase (KS)
ATAcyltransferase (AT)
DHDehydratase (DH)
EREnoylreductase (ER)
KRKetoreductase (KR)
ACPAcyl carrier (ACP)
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
EEpimerization (E)
MTMethyltransferase
TDTerminal reductase
CALCoA-ligase (CAL)
NADNAD-binding
TgrTIGR01720

Pathway Graphsteps arranged in biosynthetic order

10 steps · 9 edges
Step 1
start
+?
Step 8
Start
+6-deoxytalose
Step 9
Start
+3,4-di-O-methyl r…
Step 2M1
pks
+malonyl-CoA
Step 3M2
pks
+malonyl-CoA
Step 4M1
mps1
+Phenylalalnine
Step 5M2
mps1
+Threonine
Step 6M3
mps2
+Alanine
Step 7M4
mps2
+alaninol
Step 10
?
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions10 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1365-1start
?
[R]CCCC(O)=O
2365-2pksM1
365-1;malonyl-CoA
from: 365-1
[R]CCCC(O)CC(O)=O
3365-3pksM2
365-2;malonyl-CoA
from: 365-2
[R]CCCC(O)CCCC(O)=O
4365-4mps1M1
365-3;Phenylalalnine
from: 365-3
[R]CCCC(O)CCCC(NC(CC1=CC=CC=C1)C(O)=O)=O
5365-5mps1M2
365-4;Threonine
from: 365-4
[R]CCCC(O)CCCC(NC(CC1=CC=CC=C1)C(NC(C(O)C)C(O)=O)=O)=O
6365-6mps2M3
365-5;Alanine
from: 365-5
[R]CCCC(O)CCCC(NC(CC1=CC=CC=C1)C(NC(C(O)C)C(NC(C)C(O)=O)=O)=O)=O
7365-7mps2M4
365-6;alaninol
from: 365-6
[R]CCCC(O)CCCC(NC(CC1=CC=CC=C1)C(NC(C(O)C)C(NC(C)C(NC(C)C(O)=O)=O)=O)=O)=O
8365-8Start
6-deoxytalose
O[C@H]1[C@H](O)[C@H](O)C(O)[C@H](C)O1
9365-9Start
3,4-di-O-methyl rhamnose
O[C@H]1[C@H](O)[C@H](OC)[C@@H](OC)[C@H](C)O1
10365?
365-7;365-8;365-9
from: 365-7, 365-8, 365-9
[R]CCCC(O)CCCC(NC(CC1=CC=CC=C1)C(NC(C(O[C@H]2[C@H](O)[C@H](O)C(O)[C@H](C)O2)C)C(NC(C)C(NC(C)CO[C@H]3[C@H](O)[C@H](OC)[C@@H](OC)[C@H](C)O3)=O)=O)=O)=O
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture