Sequence of NOTN_ASPSM
EC Number:1.1.1.1
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
a primary alcohol + NAD+ = an aldehyde + NADH + H+
Other sequences found for EC No. 1.1.1.1
General information:
Sequence
0 MSLPQTYKRA VFKELGHPLT VEDAPLKLPG PNELLIKVEA CGVCYSDMYS QYNGLGGGFP
60 IVPGHEIIGK VAVVGSEVRD WNVGQRIGAG WHGGHDGTCK ACKQGYFQMC DSTAVNGATK
120 EGGYAEYTLI RSESAVHIPA NVDAASYAPI LCAGLTVFNS IRNVNIRAGE TVAVQGLGGL
180 GHLAIQYAKR MGYRVVAISR GPEKEAAARE LGADEYIDSN EGDSGEQLAA LGGAALAVTT
240 ASTGEAITPL LKGLGILGKL LVLSFPSNLT LEPTDLLKYG LSVHFWPSGH PSDAEDAVRF
300 AENTNIASVV EKFPLEQAQQ AFESMLSGKV RFRAVITMD
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
325959
Ding Y.,de Wet J.R.,Cavalcoli J.,Li S.,Greshock T.J.,Miller K.A.,Finefield J.M.,Sunderhaus J.D.,McAfoos T.J.,Tsukamoto S.,Williams R.M.,Sherman D.H.
Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp.
J. Am. Chem. Soc.
132
12733-12740
2010
325960
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
325961
Li S.,Finefield J.M.,Sunderhaus J.D.,McAfoos T.J.,Williams R.M.,Sherman D.H.
Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids.
J. Am. Chem. Soc.
134
788-791
2012
325962
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
