Bisubstrate inhibitors of 6-hydroxymethyl-7,8-dihydroptein pyrophosphokinase: Toward cell permeability.

Antibacterial Bisubstrate inhibitor Folate HPPK Pterin Transition state analog

Journal

Bioorganic & medicinal chemistry letters
ISSN: 1464-3405
Titre abrégé: Bioorg Med Chem Lett
Pays: England
ID NLM: 9107377

Informations de publication

Date de publication:
25 Sep 2024
Historique:
received: 05 07 2024
revised: 13 08 2024
accepted: 23 09 2024
medline: 28 9 2024
pubmed: 28 9 2024
entrez: 27 9 2024
Statut: aheadofprint

Résumé

6-Hydroxymethyl-7,8-dihydropterin pyrophosphokinase (HPPK) is a key enzyme in the folate biosynthesis pathway. It catalyzes the pyrophosphoryl transfer from ATP to 6-hydroxymethyl-7,8-dihydropterin (HP). HPPK is essential for microorganisms but is absent in mammals. Yet, it is not the target of any existing antibiotics. Hence, this enzyme is an attractive target for developing novel antimicrobial agents. A wealth of structural and mechanistic information has provided solid basis for structure-based design of HPPK inhibitors. Our bisubstrate inhibitors were initially created by linking 6-hydroxymethylpterin to adenosine through 2, 3, or 4 phosphate groups (HP

Identifiants

pubmed: 39332646
pii: S0960-894X(24)00379-2
doi: 10.1016/j.bmcl.2024.129977
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

129977

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Genbin Shi (G)

Center for Structural Biology, National Cancer Institute, Frederick, MD 21702, USA. Electronic address: shigenbin@mail.nih.gov.

Gary X Shaw (GX)

Center for Structural Biology, National Cancer Institute, Frederick, MD 21702, USA; Current Address: Thoracic and Gastrointestinal Malignancies Branch, National Cancer Institute, Bethesda, MD 20892, USA. Electronic address: shawg@mail.nih.gov.

Xinhua Ji (X)

Center for Structural Biology, National Cancer Institute, Frederick, MD 21702, USA.

Classifications MeSH