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Comparison of radii sets, entropy, QM methods, and sampling on MM-PBSA, MM-GBSA, and QM/MM-GBSA ligand binding energies of F. tularensis enoyl-ACP reductase (FabI)

Journal of computational chemistry, 2015-09, Vol.36 (25), p.1859-1873

2015

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Nanomole-scale protein solid-state NMR by breaking intrinsic 1H T1 boundaries

Nature methods, 2009-02, Vol.6 (3), p.215-218

2009

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Discovery of a Novel and Potent Class of F. tularensis Enoyl-Reductase (FabI) Inhibitors by Molecular Shape and Electrostatic Matching

Journal of medicinal chemistry, 2012-01, Vol.55 (1), p.268-279

2012

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Cole Relaxation Frequency as a Prognostic Parameter for Breast Cancer

Journal of patient-centered research and reviews, 2020-10, Vol.7 (4), p.343-348

2020

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Inositol Monophosphatase: A Bifunctional Enzyme in Mycobacterium smegmatis

ACS omega, 2018-10, Vol.3 (10), p.13876-13881

2018

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A novel series of enoyl reductase inhibitors targeting the ESKAPE pathogens, Staphylococcus aureus and Acinetobacter baumannii

Bioorganic & medicinal chemistry, 2018-01, Vol.26 (1), p.65-76

2018

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Ligand screening using enzymatic assays

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1140, p.291

2014

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Determination of absolute configuration and binding efficacy of benzimidazole-based FabI inhibitors through the support of electronic circular dichroism and MM-GBSA techniques

Bioorganic & medicinal chemistry letters, 2018-06, Vol.28 (11), p.2074-2079

2018

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Benzimidazole-Based FabI Inhibitors: A Promising Novel Scaffold for Anti-staphylococcal Drug Development

ACS infectious diseases, 2017-01, Vol.3 (1), p.54-61

2017

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Structural and Enzymatic Analyses Reveal the Binding Mode of a Novel Series of Francisella tularensis Enoyl Reductase (FabI) Inhibitors

Journal of medicinal chemistry, 2012-06, Vol.55 (12), p.5933-5941

2012

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A novel combinatorial biocatalytic approach for producing antibacterial compounds effective against Mycobacterium tuberculosis (TB)

Applied microbiology and biotechnology, 2013-08, Vol.97 (16), p.7151-7163

2013

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Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI)

Bioorganic & medicinal chemistry letters, 2015-03, Vol.25 (6), p.1292-1296

2015

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Structural characterization of Porphyromonas gingivalis enoyl‐ACP reductase II (FabK)

Acta crystallographica. Section F, Structural biology communications, 2018-02, Vol.74 (2), p.105-112

2018

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Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization

Acta crystallographica. Section F, Structural biology communications, 2019-10, Vol.75 (10), p.646-651

2019

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Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization. Corrigendum

Acta crystallographica. Section F, Structural biology communications, 2020-04, Vol.76 (4), p.192-193

2020

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Crystal Structure of the Nonerythroid α-Spectrin Tetramerization Site Reveals Differences between Erythroid and Nonerythroid Spectrin Tetramer Formation

The Journal of biological chemistry, 2010-05, Vol.285 (19), p.14572-14584

2010

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Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI)

Bioorganic & medicinal chemistry letters, 2015-03, Vol.25 (6)

2015

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Structural and Functional Analysis of Two Glutamate Racemase Isozymes from Bacillus anthracis and Implications for Inhibitor Design

Journal of molecular biology, 2007-08, Vol.371 (5), p.1219-1237

2007

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Metabolism-directed structure optimization of benzimidazole-based Francisella tularensis enoyl-reductase (FabI) inhibitors

Xenobiotica, 2014-05, Vol.44 (5), p.404-416

2014

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Expression, purification and characterization of enoyl-ACP reductase II, FabK, from Porphyromonas gingivalis

Protein expression and purification, 2012-09, Vol.85 (1), p.100-108

2012

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Crystal Structure of the Nonerythroid [alpha]-Spectrin Tetramerization Site Reveals Differences between Erythroid and Nonerythroid Spectrin Tetramer Formation

The Journal of biological chemistry, 2010-06, Vol.285 ((19) ; 05, 2010)

2010

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Indole trimers with antibacterial activity against Gram-positive organisms produced using combinatorial biocatalysis

AMB Express, 2015-06, Vol.5 (1), p.125-125, Article 38

2015

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Glutamate Racemase Dimerization Inhibits Dynamic Conformational Flexibility and Reduces Catalytic Rates

Biochemistry (Easton), 2009-07, Vol.48 (29), p.7045-7055

2009

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Crystal Structure of the N-terminal Region of Brain Spectrin Reveals A Helical Junction Region and A Stable Structural Domain

Biophysical journal, 2010-01, Vol.98 (3), p.248a-248a

2010

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Nanomole-scale protein solid-state NMR by breaking intrinsic 1 H T 1 boundaries

Nature methods, 2009-03, Vol.6 (3), p.215-218

2009

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Comparison of radii sets, entropy, QM methods, and sampling on MM-PBSA, MM-GBSA, and QM/MM-GBSA ligand binding energies of F. tularensis enoyl-ACP reductase (FabI)

Nanomole-scale protein solid-state NMR by breaking intrinsic 1H T1 boundaries

Discovery of a Novel and Potent Class of F. tularensis Enoyl-Reductase (FabI) Inhibitors by Molecular Shape and Electrostatic Matching

Cole Relaxation Frequency as a Prognostic Parameter for Breast Cancer

Inositol Monophosphatase: A Bifunctional Enzyme in Mycobacterium smegmatis

A novel series of enoyl reductase inhibitors targeting the ESKAPE pathogens, Staphylococcus aureus and Acinetobacter baumannii

Ligand screening using enzymatic assays

Determination of absolute configuration and binding efficacy of benzimidazole-based FabI inhibitors through the support of electronic circular dichroism and MM-GBSA techniques

Benzimidazole-Based FabI Inhibitors: A Promising Novel Scaffold for Anti-staphylococcal Drug Development

Structural and Enzymatic Analyses Reveal the Binding Mode of a Novel Series of Francisella tularensis Enoyl Reductase (FabI) Inhibitors

A novel combinatorial biocatalytic approach for producing antibacterial compounds effective against Mycobacterium tuberculosis (TB)

Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI)

Structural characterization of Porphyromonas gingivalis enoyl‐ACP reductase II (FabK)

Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization

Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: expression, purification and crystallization. Corrigendum

Crystal Structure of the Nonerythroid α-Spectrin Tetramerization Site Reveals Differences between Erythroid and Nonerythroid Spectrin Tetramer Formation

Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI)

Structural and Functional Analysis of Two Glutamate Racemase Isozymes from Bacillus anthracis and Implications for Inhibitor Design

Metabolism-directed structure optimization of benzimidazole-based Francisella tularensis enoyl-reductase (FabI) inhibitors

Expression, purification and characterization of enoyl-ACP reductase II, FabK, from Porphyromonas gingivalis

Crystal Structure of the Nonerythroid [alpha]-Spectrin Tetramerization Site Reveals Differences between Erythroid and Nonerythroid Spectrin Tetramer Formation

Indole trimers with antibacterial activity against Gram-positive organisms produced using combinatorial biocatalysis

Glutamate Racemase Dimerization Inhibits Dynamic Conformational Flexibility and Reduces Catalytic Rates

Crystal Structure of the N-terminal Region of Brain Spectrin Reveals A Helical Junction Region and A Stable Structural Domain

Nanomole-scale protein solid-state NMR by breaking intrinsic 1 H T 1 boundaries

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