Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids - Wikidata - wikimedia - TriplyDB

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

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Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

http://www.wikidata.org/entity/Q57793547

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article publié dans Nature Communications

@fr

im Oktober 2018 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published in Nature Communications

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в жовтні 2018

@uk

name

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@en

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@nl

type

label

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@en

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@nl

prefLabel

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@en

Efficient biosynthesis of heterodimeric C-aryl pyrroloindoline alkaloids

@nl

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Nature Communications

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Efficient biosynthesis of heterodimeric C3-aryl pyrroloindoline alkaloids

@en

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Dongqing Zhu

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Haidong Peng

http://www.w3.org/2001/XMLSchema#string

Mei Zheng

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Mingjia Yu

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Shi-Lu Chen

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Wenya Tian

http://www.w3.org/2001/XMLSchema#string

Yanan Zhang

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Zixin Deng

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P2860

Crystal structures and catalytic mechanism of cytochrome P450 StaP that produces the indolocarbazole skeleton

Evaluation of Biosynthetic Pathway and Engineered Biosynthesis of Alkaloids

Identification and structural basis of the reaction catalyzed by CYP121, an essential cytochrome P450 in Mycobacterium tuberculosis

Mitochondrial Lon protease in human disease and aging: Including an etiologic classification of Lon-related diseases and disorders

Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data

Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of (S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells.

Cytochrome P450 compound I: capture, characterization, and C-H bond activation kinetics.

1,2,3-Triazole-heme interactions in cytochrome P450: functionally competent triazole-water-heme complexes.

Unusual flavoenzyme catalysis in marine bacteria.

Reactive intermediates in cytochrome p450 catalysis.

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10.1038/S41467-018-06528-Z

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2018-10-24T00:00:00Z

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general chemistry

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