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Theory and applications of differential scanning fluorimetry in early-stage drug discovery

Biophysical reviews, 2020-02, Vol.12 (1), p.85-104

2020

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Repurposing the HCV NS3-4A protease drug boceprevir as COVID-19 therapeutics

RSC medicinal chemistry, 2021-04, Vol.12 (3), p.37-379

2021

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Stapled Peptides Inhibitors: A New Window for Target Drug Discovery

Computational and structural biotechnology journal, 2019-01, Vol.17, p.263-281

2019

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Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from Plasmodium falciparum reveals a distinct N-terminal domain

Nature communications, 2024-08, Vol.15 (1), p.6642-11, Article 6642

2024

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Correction: Isolation and molecular characterization of novel glucarpidases: Enzymes to improve the antibody directed enzyme pro-drug therapy for cancer treatment

PloS one, 2023-11, Vol.18 (11), p.e0294885-e0294885

2023

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The aroma of TEMED as an activation and stabilizing signal for the antibacterial enzyme HEWL

PloS one, 2020-05, Vol.15 (5), p.e0232953-e0232953

2020

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Nanoscale, automated, high throughput synthesis and screening for the accelerated discovery of protein modifiers

RSC medicinal chemistry, 2021-05, Vol.12 (5), p.89-818

2021

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Fragment Screening in the Development of a Novel Anti-Malarial

Crystals (Basel), 2023-11, Vol.13 (12), p.1610

2023

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A novel mechanism of inhibition by phenylthiourea on PvdP, a tyrosinase synthesizing pyoverdine of Pseudomonas aeruginosa

International journal of biological macromolecules, 2020-03, Vol.146, p.212-221

2020

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Novel Highlight in Malarial Drug Discovery: Aspartate Transcarbamoylase

Frontiers in cellular and infection microbiology, 2022-03, Vol.12, p.841833-841833

2022

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First crystal structures of 1-deoxy-d-xylulose 5-phosphate synthase (DXPS) from Mycobacterium tuberculosis indicate a distinct mechanism of intermediate stabilization

Scientific reports, 2022-05, Vol.12 (1), p.7221-7221, Article 7221

2022

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Isolation and molecular characterization of novel glucarpidases: Enzymes to improve the antibody directed enzyme pro-drug therapy for cancer treatment

PloS one, 2018-04, Vol.13 (4), p.e0196254

2018

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Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro

PloS one, 2018-04, Vol.13 (4), p.e0195011

2018

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Thiosulfate sulfurtransferase prevents hyperglycemic damage to the zebrafish pronephros in an experimental model for diabetes

Scientific reports, 2022-07, Vol.12 (1), p.12077-12077, Article 12077

2022

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Methods for protein characterization by mass spectrometry, thermal shift (ThermoFluor) assay, and multiangle or static light scattering

Methods in molecular biology (Clifton, N.J.), 2008, Vol.426, p.299

2008

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Thiosulfate sulfurtransferase deficiency promotes oxidative distress and aberrant NRF2 function in the brain

Redox biology, 2023-12, Vol.68, p.102965, Article 102965

2023

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The Use of Size Exclusion Chromatography to Monitor Protein Self-Assembly

Crystals (Basel), 2017-11, Vol.7 (11), p.331

2017

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Drug Target Validation Methods in Malaria - Protein Interference Assay (PIA) as a Tool for Highly Specific Drug Target Validation

Current drug targets, 2017-01, Vol.18 (9), p.1069

2017

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Structure of Mycobacterium tuberculosis 1-Deoxy-D-Xylulose 5-Phosphate Synthase in Complex with Butylacetylphosphonate

Crystals (Basel), 2023-04, Vol.13 (5), p.737

2023

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Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

Frontiers in genetics, 2022-03, Vol.13, p.782685-782685

2022

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Lipoic Acid Metabolism as a Potential Chemotherapeutic Target Against Plasmodium falciparum and Staphylococcus aureus

Frontiers in chemistry, 2021-11, Vol.9, p.742175-742175

2021

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High-resolution X-ray and NMR Structures of the SMN Tudor Domain: Conformational Variation in the Binding Site for Symmetrically Dimethylated Arginine Residues

Journal of molecular biology, 2003-03, Vol.327 (2), p.507-520

2003

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Structural Characterization and Extended Substrate Scope Analysis of Two Mg2+‐Dependent O‐Methyltransferases from Bacteria

Chembiochem : a European journal of chemical biology, 2023-05, Vol.24 (9), p.e202300076-n/a

2023

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The Crystal Structure of the Plasmodium falciparum PdxK Provides an Experimental Model for Pro-Drug Activation

Crystals (Basel), 2019-10, Vol.9 (10), p.534

2019

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Iron binding at specific sites within the octameric HbpS protects streptomycetes from iron-mediated oxidative stress

PloS one, 2013-08, Vol.8 (8), p.e71579

2013

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Theory and applications of differential scanning fluorimetry in early-stage drug discovery

Repurposing the HCV NS3-4A protease drug boceprevir as COVID-19 therapeutics

Stapled Peptides Inhibitors: A New Window for Target Drug Discovery

Cryo-EM structure of 1-deoxy-D-xylulose 5-phosphate synthase DXPS from Plasmodium falciparum reveals a distinct N-terminal domain

Correction: Isolation and molecular characterization of novel glucarpidases: Enzymes to improve the antibody directed enzyme pro-drug therapy for cancer treatment

The aroma of TEMED as an activation and stabilizing signal for the antibacterial enzyme HEWL

Nanoscale, automated, high throughput synthesis and screening for the accelerated discovery of protein modifiers

Fragment Screening in the Development of a Novel Anti-Malarial

A novel mechanism of inhibition by phenylthiourea on PvdP, a tyrosinase synthesizing pyoverdine of Pseudomonas aeruginosa

Novel Highlight in Malarial Drug Discovery: Aspartate Transcarbamoylase

First crystal structures of 1-deoxy-d-xylulose 5-phosphate synthase (DXPS) from Mycobacterium tuberculosis indicate a distinct mechanism of intermediate stabilization

Isolation and molecular characterization of novel glucarpidases: Enzymes to improve the antibody directed enzyme pro-drug therapy for cancer treatment

Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro

Thiosulfate sulfurtransferase prevents hyperglycemic damage to the zebrafish pronephros in an experimental model for diabetes

Methods for protein characterization by mass spectrometry, thermal shift (ThermoFluor) assay, and multiangle or static light scattering

Thiosulfate sulfurtransferase deficiency promotes oxidative distress and aberrant NRF2 function in the brain

The Use of Size Exclusion Chromatography to Monitor Protein Self-Assembly

Drug Target Validation Methods in Malaria - Protein Interference Assay (PIA) as a Tool for Highly Specific Drug Target Validation

Structure of Mycobacterium tuberculosis 1-Deoxy-D-Xylulose 5-Phosphate Synthase in Complex with Butylacetylphosphonate

Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

Lipoic Acid Metabolism as a Potential Chemotherapeutic Target Against Plasmodium falciparum and Staphylococcus aureus

High-resolution X-ray and NMR Structures of the SMN Tudor Domain: Conformational Variation in the Binding Site for Symmetrically Dimethylated Arginine Residues

Structural Characterization and Extended Substrate Scope Analysis of Two Mg2+‐Dependent O‐Methyltransferases from Bacteria

The Crystal Structure of the Plasmodium falciparum PdxK Provides an Experimental Model for Pro-Drug Activation

Iron binding at specific sites within the octameric HbpS protects streptomycetes from iron-mediated oxidative stress

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