FK506 Resistance of


Journal

Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061

Informations de publication

Date de publication:
01 2019
Historique:
received: 31 05 2018
accepted: 10 10 2018
pubmed: 24 10 2018
medline: 29 1 2020
entrez: 24 10 2018
Statut: epublish

Résumé

The 23-membered-ring macrolide tacrolimus, a commonly used immunosuppressant, also known as FK506, is a broad-spectrum inhibitor and an efflux pump substrate of pleiotropic drug resistance (PDR) ATP-binding cassette (ABC) transporters. Little, however, is known about the molecular mechanism by which FK506 inhibits PDR transporter drug efflux. Thus, to obtain further insights we searched for FK506-resistant mutants of

Identifiants

pubmed: 30348662
pii: AAC.01146-18
doi: 10.1128/AAC.01146-18
pmc: PMC6325234
pii:
doi:

Substances chimiques

ATP-Binding Cassette Transporters 0
Antifungal Agents 0
CDR1 protein, Candida albicans 0
Depsipeptides 0
Fungal Proteins 0
Membrane Transport Proteins 0
PDR5 protein, S cerevisiae 0
Saccharomyces cerevisiae Proteins 0
enniatins 0
beauvericin 26S048LS2R
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2018 American Society for Microbiology.

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Auteurs

Koichi Tanabe (K)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Michele Bonus (M)

Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

Susumu Tomiyama (S)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Kunji Miyoshi (K)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Minoru Nagi (M)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Kyoko Niimi (K)

Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.

Ariya Chindamporn (A)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Holger Gohlke (H)

Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

Lutz Schmitt (L)

Institute of Biochemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

Richard D Cannon (RD)

Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.

Masakazu Niimi (M)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan masa.niimi@otago.ac.nz erwin.lamping@otago.ac.nz.
Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Erwin Lamping (E)

Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand masa.niimi@otago.ac.nz erwin.lamping@otago.ac.nz.

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