EC number:2.1.1.328

Enzyme

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     2. Transferases
        2.1 Transferring one-carbon groups
            2.1.1 Methyltransferases
ID:2.1.1.328
Description:N-demethylindolmycin N-methyltransferase.

3D structure

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PDB

References

External Links

UniProtKB Enzyme Link: UniProtKB 2.1.1.328
BRENDA Enzyme Link: BRENDA 2.1.1.328
KEGG Enzyme Link: KEGG2.1.1.328
BioCyc Enzyme Link: BioCyc 2.1.1.328
ExPASy Enzyme Link: ExPASy2.1.1.328
EC2PDB Enzyme Link: EC2PDB 2.1.1.328
ExplorEnz Enzyme Link: ExplorEnz 2.1.1.328
PRIAM enzyme-specific profiles Link: PRIAM 2.1.1.328
IntEnz Enzyme Link: IntEnz 2.1.1.328
MEDLINE Enzyme Link: MEDLINE 2.1.1.328

EC number:2.1.1.328

MSA:

2.1.1.328;
Phylogenetic Tree:

2.1.1.328;
Uniprot:
M-CSA:
RHEA:24726 N-demethylindolmycin + S-adenosyl-L-methionine = H(+) + indolmycin + S-adenosyl-L-homocysteine
RULE(radius=1) [*:1]-[NH2;+0:2].[*:3]-[S+;H0:4](-[*:5])-[CH3;+0:6]>>[*:1]-[NH;+0:2]-[CH3;+0:6].[*:3]-[S;H0;+0:4]-[*:5]
Reaction
Core-to-Core No scaffolds atoms were exchanged as a result of the reaction

References

TitleAuthorsDatePubMed ID
In vitro reconstitution of indolmycin biosynthesis reveals the molecular basis of oxazolinone assembly.Du YL, Alkhalaf LM, Ryan KS2015 Mar 325730866