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cnsA

Gene
cnsA
Protein
Aurantioclavine synthase cnsA
Organism
Penicillium expansum
Length
463 amino acids
Function
FAD-linked oxidoreductase; part of the gene cluster that mediates the biosynthesis of communesins, a prominent class of indole alkaloids with great potential as pharmaceuticals (PubMed:25571861). Communesins are biosynthesized by the coupling of tryptamine and aurantioclavine, two building blocks derived from L-tryptophan (PubMed:25571861). The L-tryptophan decarboxylase cnsB converts L-tryptophan to tryptamine, whereas the tryptophan dimethylallyltransferase cnsF converts L-tryptophan to 4-dimethylallyl tryptophan which is further transformed to aurantioclavine by the aurantioclavine synthase cnsA, probably aided by the catalase cnsD (PubMed:25571861). The cytochrome P450 monooxygenase cnsC catalyzes the heterodimeric coupling between the two different indole moieties, tryptamine and aurantioclavine, to construct vicinal quaternary stereocenters and yield the heptacyclic communesin scaffold (PubMed:26963294). The O-methyltransferase cnsE then methylates the communesin scaffold to produce communesin K, the simplest characterized communesin that contains the heptacyclic core (PubMed:25571861). The dioxygenase cnsJ converts communesin K into commmunesin I (PubMed:25571861). Acylation to introduce the hexadienyl group at position N16 of communesin I by the acyltransferase cnsK leads to the production of communesin B. The hexadienyl group is produced by the highly reducing polyketide synthase cnsI, before being hydrolytically removed from cnsI by the serine hydrolase cnsH, converted into hexadienyl-CoA by the CoA ligase cnsG, and then transferred to commmunesin I by cnsK (PubMed:25571861). Surprisingly, cnsK may also be a promiscuous acyltransferase that can tolerate a range of acyl groups, including acetyl-, propionyl-, and butyryl-CoA, which lead to communesins A, G and H respectively (PubMed:25571861). The roles of the alpha-ketoglutarate-dependent dioxygenases cnsM and cnsP have still to be determined (PubMed:25571861).
Similarity
Belongs to the oxygen-dependent FAD-linked oxidoreductase family.
Mass
51.122 kDa
Sequence
MEGCTTRDSTGLGLGERFNQRGNVFLRLVSHVQCAIKFAKNHNLRLVIRNTGHDGSGRSSAPGSFEIHTHHLKHTHYHDDFQPVGAVTTSGPAVTVGAGVILGDLYAEGARQGYTVVGGVCPTVGFVGGFLQGGGVSGKFSHNRGLAVDNVLEIQAVTADGDLVVANDYHNQDLFWALRGGGGGTFAVVTQATVRVFPDVPCVTTQLAVSAPEGLDDHSWMQVLELLLRGLRSFNEERIAGEFHLRPDPLSAILTLHFLNTSDLDSVDRRLAALIDKFRTSEIPHIYSSKSHALEVPRSVEAKLYASHELTSVQMPVLYSLDPSYKVSYLNMGDPNDADFRNVYWGPNYERLLALKQKWDVDALFITRLGKRHDVMNTIPSTGAGADMRSFNRDIYDLLRNHAEDPRLNEVWTAINTVTEWVDWITSNGARMIPSDIAFRFWMLRVYMTHDWGCGLTSSTAEL

Gene
cnsA
Protein
1,8-cineole synthase
Organism
Streptomyces clavuligerus (strain ATCC 27064 / DSM 738 / JCM 4710 / NBRC 13307 / NCIMB 12785 / NRRL 3585 / VKM Ac-602)
Length
330 amino acids
Function
In vitro, catalyzes the formation of 1,8-cineole from geranyl diphosphate (GPP) (PubMed:21726035, PubMed:28144299, PubMed:28966840). Can also accept neryl diphosphate (NPP) as substrate to produce 1,8-cineole (PubMed:28966840).
Similarity
Belongs to the terpene synthase family.
Mass
37.725 kDa
Sequence
MPAGHEEFDIPFPSRVNPFHARAEDRHVAWMRAMGLITGDAAEATYRRWSPAKVGARWFYLAQGEDLDLGCDIFGWFFAYDDHFDGPTGTDPRQTAAFVNRTVAMLDPRADPTGEHPLNIAFHDLWQRESAPMSPLWQRRAVDHWTQYLTAHITEATNRTRHTSPTIADYLELRHRTGFMPPLLDLIERVWRAEIPAPVYTTPEVQTLLHTTNQNINIVNDVLSLEKEEAHGDPHNLVLVIQHERQSTRQQALATARRMIDEWTDTFIRTEPRLPALCGRLGIPLADRTSLYTAVEGMRAAIRGNYDWCAETNRYAVHRPTGTGRATTPW