Sequence of CXE1_PAPSO
EC Number:3.1.1.105
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
3-O-acetylpapaveroxine + H2O = narcotine hemiacetal + acetate
Other sequences found for EC No. 3.1.1.105
General information:
Sequence
0 MADPYEFLMC IHNPEEDTLT RNFPIPATPL DQNTKDISLN PDRKTSLRIF RPPTKEPPVT
60 KNKLLPIIIY FHGGGFILFN ADSTMNHDFC QSIATHIPAL VVSVDYRLAP ENRLPAAYDD
120 AVDALNWVKD QGLGKLNNSE VWLKEYGDFS KCFIMGCSSG ANVAYHASLR AIEMDLEPAK
180 INGLILHCPF FGSLERTESD SKVINNQDLP LAVRDVMWEL ALPLGSTRDH VYCNPNIDHD
240 GSSSGNMVGL IERCFVVGFY GDPLIDRQIQ LVKMLEEKGV KVETWIEQGG YHGVLCFDPM
300 IRETFLEKLK HFILNDEFIY
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
786447
Winzer T.,Gazda V.,He Z.,Kaminski F.,Kern M.,Larson T.R.,Li Y.,Meade F.,Teodor R.,Vaistij F.E.,Walker C.,Bowser T.A.,Graham I.A.
A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine.
Science
336
1704-1708
2012
786448
Dang T.T.,Chen X.,Facchini P.J.
Acetylation serves as a protective group in noscapine biosynthesis in opium poppy.
Nat. Chem. Biol.
11
104-106
2015
786449
Li Y.,Smolke C.D.
Engineering biosynthesis of the anticancer alkaloid noscapine in yeast.
Nat. Commun.
7
12137-12137
2016
786450
Li Y.,Li S.,Thodey K.,Trenchard I.,Cravens A.,Smolke C.D.
Complete biosynthesis of noscapine and halogenated alkaloids in yeast.
Proc. Natl. Acad. Sci. U.S.A.
115
0-0
2018
