Sequence of NOTF_ASPVE
EC Number:2.5.1.109
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
brevianamide F prenyltransferase (deoxybrevianamide E-forming)
I4AY86
Aspergillus versicolor
435
49567
Reaction
dimethylallyl diphosphate + brevianamide F = diphosphate + deoxybrevianamide E
Other sequences found for EC No. 2.5.1.109
General information:
Sequence
0 MTAPELRAPA GHPQEPPARS SPAQALSSYH HFPTSDQERW YQETGSLCSR FLEAGQYGLH
60 QQYQFMFFFM HHLIPALGPY PQKWRSTISR SGLPIEFSLN FQKGSHRLLR IGFEPVNFLS
120 GSSQDPFNRI PIADLLAQLA RLQLRGFDTQ CFQQLLTRFQ LSLDEVRQLP PDDQPLKSQG
180 AFGFDFNPDG AILVKGYVFP YLKAKAAGVP VATLIAESVR AIDADRNQFM HAFSLINDYM
240 QESTGYNEYT FLSCDLVEMS RQRVKIYGAH TEVTWAKIAE MWTLGGRLIE EPEIMEGLAR
300 LKQIWSLLQI GEGSRAFKGG FDYGKASATD QIPSPIIWNY EISPGSSFPV PKFYLPVHGE
360 NDLRVARSLA QFWDSLGWSE HACAYPDMLQ QLYPDLDVSR TSRLQSWISY SYTAKKGVYM
420 SVYFHSQSTY LWEED
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
325912
Yin S.,Yu X.,Wang Q.,Liu X.Q.,Li S.M.
Identification of a brevianamide F reverse prenyltransferase BrePT from Aspergillus versicolor with a broad substrate specificity towards tryptophan-containing cyclic dipeptides.
Appl. Microbiol. Biotechnol.
97
1649-1660
2013
325913
Li S.,Anand K.,Tran H.,Yu F.,Finefield J.M.,Sunderhaus J.D.,McAfoos T.J.,Tsukamoto S.,Williams R.M.,Sherman D.H.
Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways.
Med. Chem. Commun.
3
987-996
2012
325914
Kato H.,Yoshida T.,Tokue T.,Nojiri Y.,Hirota H.,Ohta T.,Williams R.M.,Tsukamoto S.
Notoamides A-D: prenylated indole alkaloids isolated from a marine-derived fungus, Aspergillus sp.
Angew. Chem. Int. Ed.
46
2254-2256
2007
