Enzyme

Download
EC Tree
     6. Ligases
        6.3 Forming carbon-nitrogen bonds
            6.3.2 Acid-D-amino-acid ligases (peptide synthases)
ID:6.3.2.40
Description:Cyclopeptine synthase.

3D structure

Click one PDB to see exact 3D structure provided by NGL.

Note: Use your mouse to drag, rotate, and zoom in and out of the structure. Mouse-over to identify atoms and bonds. Mouse controls documentation.

References

External Links

UniProtKB Enzyme Link: UniProtKB 6.3.2.40
BRENDA Enzyme Link: BRENDA 6.3.2.40
KEGG Enzyme Link: KEGG6.3.2.40
BioCyc Enzyme Link: BioCyc 6.3.2.40
ExPASy Enzyme Link: ExPASy6.3.2.40
EC2PDB Enzyme Link: EC2PDB 6.3.2.40
ExplorEnz Enzyme Link: ExplorEnz 6.3.2.40
PRIAM enzyme-specific profiles Link: PRIAM 6.3.2.40
IntEnz Enzyme Link: IntEnz 6.3.2.40
MEDLINE Enzyme Link: MEDLINE 6.3.2.40
MSA:

6.3.2.40;

Phylogenetic Tree:

6.3.2.40;

Uniprot:
M-CSA:
RHEA:35091 anthranilate + 2 ATP + L-phenylalanine + S-adenosyl-L-methionine = 2 AMP + cyclopeptine + 2 diphosphate + 2 H(+) + S-adenosyl-L-homocysteine
RULE(radius=1) [*:1]-[O;H0;+0:2]-[P;H0;+0:3](-[*:4])(=[*:5])-[*:6].[*:7]-[P;H0;+0:8](=[*:9])(-[*:10])-[O;H0;+0:11]-[*:12].[*:13]-[S+;H0:14](-[*:15])-[CH3;+0:16].[*:17]=[C;H0;+0:18](-[OH;+0:19])-[*:20]-[NH2;+0:21].[*:22]=[C;H0;+0:23](-[OH;+0:24])-[*:25]:[*:26]-[NH2;+0:27]>>[*:1]-[OH;+0:2].[*:12]-[OH;+0:11].[*:4]-[P;H0;+0:3](=[*:5])(-[*:6])-[OH;+0:19].[*:7]-[P;H0;+0:8](=[*:9])(-[*:10])-[OH;+0:24].[*:13]-[S;H0;+0:14]-[*:15].[*:22]=[C;H0;+0:23]1-[*:25]:[*:26]-[NH;+0:27]-[C;H0;+0:18](=[*:17])-[*:20]-[N;H0;+0:21]-1-[CH3;+0:16]
Reaction
Core-to-Core More

References

TitleAuthorsDatePubMed ID
Cyclopeptine synthetase activity in surface cultures of Penicillium cyclopium.Lerbs W, Luckner M19852995633
Uric acid is a genuine metabolite of Penicillium cyclopium and stimulates the expression of alkaloid biosynthesis in this fungus.Helbig F, Steighardt J, Roos W2002 Apr11916664