EC Tree |
2. Transferases |
2.5 Transferring alkyl or aryl groups, other than methyl groups |
2.5.1 Transferring alkyl or aryl groups, other than methyl groups (only sub-subclass identified to date) |
ID: | 2.5.1.124 |
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Description: | 6-linalyl-2-O,3-dimethylflaviolin synthase. |
Alternative Name: |
methylnaphthalene-1,4-dione synthase. 6-(3,7-dimethylocta-1,6-dien-3-yl)-5,7-dihydroxy-2-methoxy-3- |
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.UniProtKB Enzyme Link: | UniProtKB 2.5.1.124 |
BRENDA Enzyme Link: | BRENDA 2.5.1.124 |
KEGG Enzyme Link: | KEGG2.5.1.124 |
BioCyc Enzyme Link: | BioCyc 2.5.1.124 |
ExPASy Enzyme Link: | ExPASy2.5.1.124 |
EC2PDB Enzyme Link: | EC2PDB 2.5.1.124 |
ExplorEnz Enzyme Link: | ExplorEnz 2.5.1.124 |
PRIAM enzyme-specific profiles Link: | PRIAM 2.5.1.124 |
IntEnz Enzyme Link: | IntEnz 2.5.1.124 |
MEDLINE Enzyme Link: | MEDLINE 2.5.1.124 |
MSA: | |
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Phylogenetic Tree: | |
Uniprot: | |
M-CSA: |
RHEA:41007 | (2E)-geranyl diphosphate + 2-O,3-dimethylflaviolin = 6-linalyl-2-O,3-dimethylflaviolin + diphosphate |
RULE(radius=1) | [*:1]-[C;H0;+0:2](-[*:3])=[CH;+0:4]-[CH2;+0:5]-[O;H0;+0:6]-[*:7].[*:8]:[cH;+0:9]:[*:10]>>[*:1]-[C;H0;+0:2](-[*:3])(-[CH;+0:4]=[CH2;+0:5])-[c;H0;+0:9](:[*:8]):[*:10].[*:7]-[OH;+0:6] |
Reaction | ![]() |
Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
Title | Authors | Date | PubMed ID |
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Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products. | Kumano T, Tomita T, Nishiyama M, Kuzuyama T | 2010 Dec 17 | 20937800 |