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Biochemical and structural investigations on phosphoribosylpyrophosphate synthetase from Mycobacterium smegmatis

PloS one, 2017-04, Vol.12 (4), p.e0175815-e0175815

2017

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Mycobacterium tuberculosis Pathogenesis, Infection Prevention and Treatment

Pathogens (Basel), 2020-05, Vol.9 (5), p.385

2020

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Structural investigations on orotate phosphoribosyltransferase from Mycobacterium tuberculosis, a key enzyme of the de novo pyrimidine biosynthesis

Scientific reports, 2017-04, Vol.7 (1), p.1180-11, Article 1180

2017

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A Selective Competitive Inhibitor of Aldehyde Dehydrogenase 1A3 Hinders Cancer Cell Growth, Invasiveness and Stemness In Vitro

Cancers, 2021-01, Vol.13 (2), p.356

2021

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The integration of AlphaFold-predicted and crystal structures of human trans-3-hydroxy-l-proline dehydratase reveals a regulatory catalytic mechanism

Computational and structural biotechnology journal, 2022-01, Vol.20, p.3874-3883

2022

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The Synthesis of Kynurenic Acid in Mammals: An Updated Kynurenine Aminotransferase Structural KATalogue

Frontiers in molecular biosciences, 2019-02, Vol.6, p.7-7

2019

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Mycobacterium tuberculosis Molecular Determinants of Infection, Survival Strategies, and Vulnerable Targets

Pathogens (Basel), 2018-02, Vol.7 (1), p.17

2018

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Curcumin-based-fluorescent probes targeting ALDH1A3 as a promising tool for glioblastoma precision surgery and early diagnosis

Communications biology, 2022-09, Vol.5 (1), p.895-895, Article 895

2022

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Extracellular NAD+ enhances PARP-dependent DNA repair capacity independently of CD73 activity

Scientific reports, 2020-01, Vol.10 (1), p.651-651, Article 651

2020

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Biochemical characterization of Mycobacterium tuberculosis dihydroorotate dehydrogenase and identification of a selective inhibitor

FEBS letters, 2023-08, Vol.597 (16), p.2119-2132

2023

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Structure of Thermococcus litoralis trans-3-hydroxy-l-proline dehydratase in the free and substrate-complexed form

Biochemical and biophysical research communications, 2019-08, Vol.516 (1), p.189-195

2019

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Structure of Thermococcus litoralis Δ 1 -pyrroline-2-carboxylate reductase in complex with NADH and L-proline

Acta crystallographica. Section D, Structural biology, 2020-05, Vol.76 (Pt 5), p.496-505

2020

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Structure of Thermococcus litoralis Δ1‐pyrroline‐2‐carboxylate reductase in complex with NADH and l‐proline

Acta crystallographica. Section D, Biological crystallography., 2020-05, Vol.76 (5), p.496-505

2020

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Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2‑Hydroxypyrazolo[1,5‑a]pyridine Scaffold: SAR of the Aryloxyaryl Moiety

Journal of medicinal chemistry, 2022-10, Vol.65 (19), p.12701-12724

2022

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An alternative conformation of the N‐terminal loop of human dihydroorotate dehydrogenase drives binding to a potent antiproliferative agent

Acta crystallographica. Section D, Biological crystallography., 2024-06, Vol.80 (6), p.386-396

2024

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Hit discovery of Mycobacterium tuberculosis inosine 5′-monophosphate dehydrogenase, GuaB2, inhibitors

Bioorganic & medicinal chemistry letters, 2018-06, Vol.28 (10), p.1714-1718

2018

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Structures of citrate synthase and malate dehydrogenase of Mycobacterium tuberculosis

Proteins, structure, function, and bioinformatics, 2015-02, Vol.83 (2), p.389-394

2015

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Targeting NAD-dependent dehydrogenases in drug discovery against infectious diseases and cancer

Biochemical Society transactions, 2020-04, Vol.48 (2), p.693-707

2020

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Expanding Benzoxazole-Based Inosine 5′-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure–Activity As Potential Antituberculosis Agents

Journal of medicinal chemistry, 2018-06, Vol.61 (11), p.4739-4756

2018

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Design, synthesis, SAR and biological investigation of 3-(carboxymethyl)rhodanine and aminothiazole inhibitors of Mycobacterium tuberculosis Zmp1

Bioorganic & medicinal chemistry letters, 2018-02, Vol.28 (4), p.637-641

2018

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Crystal structure of the Mycobacterium tuberculosis phosphate binding protein PstS3

Proteins, structure, function, and bioinformatics, 2014-09, Vol.82 (9), p.2268-2274

2014

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Expanding Benzoxazole-Based Inosine 5′-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure–Activity As Potential Antituberculosis Agents

Journal of medicinal chemistry, 2021-12, Vol.64 (24), p.18233-18234

2021

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Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH

European journal of medicinal chemistry, 2019-07, Vol.174, p.309-329

2019

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Discovery of the first potent and selective Mycobacterium tuberculosis Zmp1 inhibitor

Bioorganic & medicinal chemistry letters, 2014-06, Vol.24 (11), p.2508-2511

2014

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Biochemical and structural investigations on phosphoribosylpyrophosphate synthetase from Mycobacterium smegmatis

Mycobacterium tuberculosis Pathogenesis, Infection Prevention and Treatment

Structural investigations on orotate phosphoribosyltransferase from Mycobacterium tuberculosis, a key enzyme of the de novo pyrimidine biosynthesis

A Selective Competitive Inhibitor of Aldehyde Dehydrogenase 1A3 Hinders Cancer Cell Growth, Invasiveness and Stemness In Vitro

The integration of AlphaFold-predicted and crystal structures of human trans-3-hydroxy-l-proline dehydratase reveals a regulatory catalytic mechanism

The Synthesis of Kynurenic Acid in Mammals: An Updated Kynurenine Aminotransferase Structural KATalogue

Mycobacterium tuberculosis Molecular Determinants of Infection, Survival Strategies, and Vulnerable Targets

Curcumin-based-fluorescent probes targeting ALDH1A3 as a promising tool for glioblastoma precision surgery and early diagnosis

Extracellular NAD+ enhances PARP-dependent DNA repair capacity independently of CD73 activity

Biochemical characterization of Mycobacterium tuberculosis dihydroorotate dehydrogenase and identification of a selective inhibitor

Structure of Thermococcus litoralis trans-3-hydroxy-l-proline dehydratase in the free and substrate-complexed form

Structure of Thermococcus litoralis Δ 1 -pyrroline-2-carboxylate reductase in complex with NADH and L-proline

Structure of Thermococcus litoralis Δ1‐pyrroline‐2‐carboxylate reductase in complex with NADH and l‐proline

Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2‑Hydroxypyrazolo[1,5‑a]pyridine Scaffold: SAR of the Aryloxyaryl Moiety

An alternative conformation of the N‐terminal loop of human dihydroorotate dehydrogenase drives binding to a potent antiproliferative agent

Hit discovery of Mycobacterium tuberculosis inosine 5′-monophosphate dehydrogenase, GuaB2, inhibitors

Structures of citrate synthase and malate dehydrogenase of Mycobacterium tuberculosis

Targeting NAD-dependent dehydrogenases in drug discovery against infectious diseases and cancer

Expanding Benzoxazole-Based Inosine 5′-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure–Activity As Potential Antituberculosis Agents

Design, synthesis, SAR and biological investigation of 3-(carboxymethyl)rhodanine and aminothiazole inhibitors of Mycobacterium tuberculosis Zmp1

Crystal structure of the Mycobacterium tuberculosis phosphate binding protein PstS3

Expanding Benzoxazole-Based Inosine 5′-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure–Activity As Potential Antituberculosis Agents

Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH

Discovery of the first potent and selective Mycobacterium tuberculosis Zmp1 inhibitor

Development of Potent Inhibitors of the Mycobacterium tuberculosis Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside Macrophages

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