Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

about

Computational approaches for de novo design and redesign of metal-binding sites on proteins Imino Transfer Hydrogenation Reductions.Biocatalyst-artificial metalloenzyme cascade based on alcohol dehydrogenase

P2860

Q30398300-9166B2A4-1814-41A9-9AAD-A4FC19467E92 Q38940186-708723B2-D841-498D-B9CB-01C103530D36 Q57470003-F126D019-E2A3-4AF0-B891-BB2729A45D89

P2860

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

Item

http://www.wikidata.org/entity/Q57786604

description

im Januar 2015 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована у 2015

@uk

name

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@en

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@nl

type

Item

label

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@en

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@nl

prefLabel

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@en

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@nl

P1476

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

@en

P2093

Tommaso Quinto

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

Valentin Köhler

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

P2860

Artificial transfer hydrogenases for the enantioselective reduction of cyclic imines

Structure and activity of NADPH-dependent reductase Q1EQE0 from Streptomyces kanamyceticus, which catalyses the R-selective reduction of an imine substrate

Structural, kinetic, and docking studies of artificial imine reductases based on biotin-streptavidin technology: an induced lock-and-key hypothesis

Biotransformations monitored in situ by proton nuclear magnetic resonance spectroscopy.

Engineering the third wave of biocatalysis.

Stereochemical course of two arene-cis-diol dehydrogenases specifically induced in Pseudomonas putida.

Stereoselective preparation of deuterated reduced nicotinamide adenine nucleotides and substrates by enzymatic synthesis.

Synthetic cascades are enabled by combining biocatalysts with artificial metalloenzymes.

Towards recyclable NAD(P)H regeneration catalysts.

Asymmetric Reduction of Cyclic Imines Catalyzed by a Whole-Cell Biocatalyst Containing an (S)-Imine Reductase

P304

357-360

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

P31

scholarly article

P356

10.1039/C4OB02071E

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

P433

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

P478

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

P50

Daniel Häussinger

Thomas R Ward

P577

2015-01-01T00:00:00Z

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

P698

25379837

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

P921

diastereoselectivity

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

about

P2860

P2860

Artificial metalloenzymes for the diastereoselective reduction of NAD+ to NAD2H

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921