Structure-based design of NAD+ analogues targeting bacterial NAD kinases, promising targets for new antibiotics

被引：0

作者：

Rahimova, R. ^{[1
]}

Nogaret, P. ^{[2
]}

Huteau, V. ^{[3
]}

Leseigneur, C. ^{[4
]}

Gelin, M. ^{[1
]}

Clement, D. ^{[3
]}

Dussurget, O. ^{[4
]}

Labesse, G. ^{[1
]}

Pochet, S. ^{[3
]}

Blanc-Potard, A. ^{[2
]}

Lionne, C. ^{[1
]}

机构：

[1] Univ Montpellier, Ctr Biol Struct CBS, CNRS, INSERM,UMR 5048,U1054, Montpellier, France

[2] Univ Montpellier, CNRS, UMR 5235, Lab Pathogen Host Interact LPHI, Montpellier, France

[3] Univ Paris, Inst Pasteur, CNRS, UMR3523,Unite Chim Biol Epigenet, Paris, France

[4] Univ Paris, Inst Pasteur, Sorbonne Paris Cite, Unite Rech Yersinia, Paris, France

来源：

FEBS OPEN BIO | 2022年 / 12卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

ShT-02.2-5

引用

页码：24 / 24

页数：1

共 35 条

[1] Structure-based design, synthesis and biological evaluation of a NAD+ analogue targeting Pseudomonas aeruginosa NAD kinase
Rahimova, Rahila
Nogaret, Pauline
Huteau, Valerie
Gelin, Muriel
Clement, David A.
Labesse, Gilles
Pochet, Sylvie
Blanc-Potard, Anne-Beatrice
Lionne, Corinne
FEBS JOURNAL, 2023, 290 (02) : 482 - 501
[2] Targeting NAD Biosynthesis in Bacterial Pathogens: Structure-Based Development of Inhibitors of Nicotinate Mononucleotide Adenylyltransferase NadD
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[3] Structure-based design of agents targeting the bacterial ribosome
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Matassova, N
Murchie, A
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[4] The bacterial ribosome, a promising focus for structure-based drug design
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[5] Structure-Based Design of Promysalin Analogues to Overcome Mechanisms of Bacterial Resistance
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ACS OMEGA, 2023, 8 (13): : 12558 - 12564
[6] Protein kinases as targets for antimalarial intervention: Kinomics, structure-based design, transmission-blockade, and targeting host cell enzymes
Doerig, C
Billker, O
Pratt, D
Endicott, J
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2005, 1754 (1-2): : 132 - 150
[7] Structure-based design of guanosine analogue inhibitors targeting GTP cyclohydrolase IB towards a new class of antibiotics
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Hecht, David A.
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BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2020, 30 (02)
[8] Structure-based design of inhibitors of the riboflavin pathway targeting the bacterial FMN riboswitch
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[9] Structure-based design and synthesis of dipeptide analogues as new inhibitors of leucine aminopeptidase
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PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 2002, 177 (6-7) : 1739 - 1743
[10] Identification through structure-based methods of a bacterial NAD+-dependent DNA ligase inhibitor that avoids known resistance mutations
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