A journey into the regulatory secrets of the de novo purine nucleotide biosynthesis

被引:0
|
作者
Ayoub, Nour [1 ]
Gedeon, Antoine [2 ]
Munier-Lehmann, Helene [1 ]
机构
[1] Univ Paris Cite, Inst Pasteur, UMRS 1124, INSERM, Paris, France
[2] Univ PSL, Sorbonne Univ, Ecole Normale Super, UMR7203,CNRS,LBM, Paris, France
关键词
allostery; antibacterial agents; chemical compounds; enzyme regulation; IMP dehydrogenase; nucleotide biosynthesis; protein-protein interactions; protein structure-function relationship; INOSINE 5'-MONOPHOSPHATE DEHYDROGENASE; GLUTAMINE PHOSPHORIBOSYLPYROPHOSPHATE AMIDOTRANSFERASE; FORMYLGLYCINAMIDE RIBONUCLEOTIDE AMIDOTRANSFERASE; PROTEIN-PROTEIN INTERACTION; DOMINANT RETINITIS-PIGMENTOSA; LARGE-SCALE IDENTIFICATION; ESCHERICHIA-COLI; BACILLUS-SUBTILIS; ADENYLOSUCCINATE SYNTHETASE; IMP DEHYDROGENASE;
D O I
10.3389/fphar.2024.1329011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
De novo purine nucleotide biosynthesis (DNPNB) consists of sequential reactions that are majorly conserved in living organisms. Several regulation events take place to maintain physiological concentrations of adenylate and guanylate nucleotides in cells and to fine-tune the production of purine nucleotides in response to changing cellular demands. Recent years have seen a renewed interest in the DNPNB enzymes, with some being highlighted as promising targets for therapeutic molecules. Herein, a review of two newly revealed modes of regulation of the DNPNB pathway has been carried out: i) the unprecedent allosteric regulation of one of the limiting enzymes of the pathway named inosine 5'-monophosphate dehydrogenase (IMPDH), and ii) the supramolecular assembly of DNPNB enzymes. Moreover, recent advances that revealed the therapeutic potential of DNPNB enzymes in bacteria could open the road for the pharmacological development of novel antibiotics.
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页数:30
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