(Q40024861)

English

Structure-Based Insight into the Asymmetric Bioreduction of the C=C Double Bond of alpha,beta-Unsaturated Nitroalkenes by Pentaerythritol Tetranitrate Reductase

scientific article published on November 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Structure-Based Insight into the Asymmetric Bioreduction of the C=C Double Bond of alpha,beta-Unsaturated Nitroalkenes by Pentaerythritol Tetranitrate Reductase (English)

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

pentaerythritol tetranitrate

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based on heuristic

inferred from title

Anna Fryszkowska

2

0 references

Helen S Toogood

1

0 references

Gill M. Stephens

8

0 references

9

object named as

Nigel S Scrutton

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Anna Roujeinikova

5

object named as

Anna Roujeinikova

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

author name string

Victoria Hare

3

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Karl Fisher

4

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

David Leys

6

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

John M Gardiner

7

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

publication date

1 November 2008

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Europe PubMed Central

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16 September 2017

Advanced Synthesis & Catalysis

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Europe PubMed Central

PMC publication ID

16 September 2017

350

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

17

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

2789-2803

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Highly enantioselective reduction of beta,beta-disubstituted aromatic nitroalkenes catalyzed by Clostridium sporogenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

The Amber biomolecular simulation programs

1 reference

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22 September 2017

Conjugate additions of nitroalkanes to electron-poor alkenes: recent results

1 reference

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Involvement of a flavosemiquinone in the enzymatic oxidation of nitroalkanes catalyzed by 2-nitropropane dioxygenase

1 reference

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Coot: model-building tools for molecular graphics

1 reference

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22 September 2017

Refinement of macromolecular structures by the maximum-likelihood method

1 reference

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22 September 2017

The CCP4 suite: programs for protein crystallography

1 reference

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22 September 2017

Development and testing of a general amber force field

1 reference

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22 September 2017

'New uses for an Old Enzyme'--the Old Yellow Enzyme family of flavoenzymes

1 reference

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22 September 2017

Kinetic and structural basis of reactivity of pentaerythritol tetranitrate reductase with NADPH, 2-cyclohexenone, nitroesters, and nitroaromatic explosives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Cloning of nitroalkane oxidase from Fusarium oxysporum identifies a new member of the acyl-CoA dehydrogenase superfamily.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Crystal structure of pentaerythritol tetranitrate reductase: "flipped" binding geometries for steroid substrates in different redox states of the enzyme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Old yellow enzyme: stepwise reduction of nitro-olefins and catalysis of aci-nitro tautomerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Flavoenzymes: diverse catalysts with recurrent features

1 reference

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22 September 2017

Automated protein model building combined with iterative structure refinement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Sequence and properties of pentaerythritol tetranitrate reductase from Enterobacter cloacae PB2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Old yellow enzyme at 2 A resolution: overall structure, ligand binding, and comparison with related flavoproteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Propionate-3-nitronate oxidase from Penicillium atrovenetum is a flavoprotein which initiates the autoxidation of its substrate by O2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Determination of dissociation constants and specific rate constants of enzyme-substrate (or protein-ligand) interactions from rapid reaction kinetic data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

22 September 2017

Biotransformation of explosives by the old yellow enzyme family of flavoproteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

25 September 2017

The mechanism of oxidation of nitroalkanes by horseradish peroxidase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

15 June 2018

Opposite stereochemical courses for enzyme-mediated alkene reductions of an enantiomeric substrate pair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Asymmetric alkene reduction by yeast old yellow enzymes and by a novel Zymomonas mobilis reductase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Stereospecific alkyne reduction: novel activity of old yellow enzymes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Proton transfer in the oxidative half-reaction of pentaerythritol tetranitrate reductase. Structure of the reduced enzyme-progesterone complex and the roles of residues Tyr186, His181, His184.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Role of active site residues and solvent in proton transfer and the modulation of flavin reduction potential in bacterial morphinone reductase.

1 reference

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20 August 2018

Reaction of morphinone reductase with 2-cyclohexen-1-one and 1-nitrocyclohexene: proton donation, ligand binding, and the role of residues Histidine 186 and Asparagine 189.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Atomic resolution structures and solution behavior of enzyme-substrate complexes of Enterobacter cloacae PB2 pentaerythritol tetranitrate reductase. Multiple conformational states and implications for the mechanism of nitroaromatic explosive degrada

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

H-tunneling in the multiple H-transfers of the catalytic cycle of morphinone reductase and in the reductive half-reaction of the homologous pentaerythritol tetranitrate reductase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

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CYP83b1 is the oxime-metabolizing enzyme in the glucosinolate pathway in Arabidopsis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2854801

20 August 2018

Enoate reductases of Clostridia. Cloning, sequencing, and expression

1 reference

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20 August 2018

Old Yellow enzyme: aromatization of cyclic enones and the mechanism of a novel dismutation reaction.

1 reference

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20 August 2018

Stereocomplementary Bioreduction of α,β-Unsaturated Dicarboxylic Acids and Dimethyl Esters using Enoate Reductases: Enzyme- and Substrate-Based Stereocontrol

1 reference

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Asymmetric Bioreduction of Activated Alkenes Using Cloned 12-Oxophytodienoate Reductase Isoenzymes OPR-1 and OPR-3 fromLycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity

1 reference

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

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Crystallization and preliminary diffraction studies of pentaerythritol tetranitrate reductase from Enterobacter cloacae PB2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic Enantioselective Conjugate Reduction ofβ,β-Disubstituted Nitroalkenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalytic asymmetric transfer hydrogenation of nitroolefins

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient Cu-catalyzed asymmetric conjugate additions of alkylzinc reagents to aromatic and aliphatic acyclic nitroalkenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The oxidative half-reaction of Old Yellow Enzyme. The role of tyrosine 196

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Convenient Catalytic, Enantioselective Conjugate Reduction of Nitroalkenes Using CuF2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective synthesis of nitroalkanes bearing all-carbon quaternary stereogenic centers through Cu-catalyzed asymmetric conjugate additions

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KINETICS AND MECHANISM OF ACTION OF GLUCOSE OXIDASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/20396603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ADSC.200800561

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Europe PubMed Central

PMC publication ID

16 September 2017

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24 November 2022

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PMC publication ID

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Europe PubMed Central

PMC publication ID

16 September 2017

PubMed publication ID

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Europe PubMed Central

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16 September 2017

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