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FKBP Ligands—Where We Are and Where to Go?

In recent years, many members of the FK506-binding protein (FKBP) family were increasingly linked to various diseases. The binding domain of FKBPs differs only in a few amino acid residues, but their biological roles are versatile. High-affinity ligands with selectivity between close homologs are sc...

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Detalles Bibliográficos
Autores principales: Kolos, Jürgen M., Voll, Andreas M., Bauder, Michael, Hausch, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290070/
https://www.ncbi.nlm.nih.gov/pubmed/30568592
http://dx.doi.org/10.3389/fphar.2018.01425
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author Kolos, Jürgen M.
Voll, Andreas M.
Bauder, Michael
Hausch, Felix
author_facet Kolos, Jürgen M.
Voll, Andreas M.
Bauder, Michael
Hausch, Felix
author_sort Kolos, Jürgen M.
collection PubMed
description In recent years, many members of the FK506-binding protein (FKBP) family were increasingly linked to various diseases. The binding domain of FKBPs differs only in a few amino acid residues, but their biological roles are versatile. High-affinity ligands with selectivity between close homologs are scarce. This review will give an overview of the most prominent ligands developed for FKBPs and highlight a perspective for future developments. More precisely, human FKBPs and correlated diseases will be discussed as well as microbial FKBPs in the context of anti-bacterial and anti-fungal therapeutics. The last section gives insights into high-affinity ligands as chemical tools and dimerizers.
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spelling pubmed-62900702018-12-19 FKBP Ligands—Where We Are and Where to Go? Kolos, Jürgen M. Voll, Andreas M. Bauder, Michael Hausch, Felix Front Pharmacol Pharmacology In recent years, many members of the FK506-binding protein (FKBP) family were increasingly linked to various diseases. The binding domain of FKBPs differs only in a few amino acid residues, but their biological roles are versatile. High-affinity ligands with selectivity between close homologs are scarce. This review will give an overview of the most prominent ligands developed for FKBPs and highlight a perspective for future developments. More precisely, human FKBPs and correlated diseases will be discussed as well as microbial FKBPs in the context of anti-bacterial and anti-fungal therapeutics. The last section gives insights into high-affinity ligands as chemical tools and dimerizers. Frontiers Media S.A. 2018-12-05 /pmc/articles/PMC6290070/ /pubmed/30568592 http://dx.doi.org/10.3389/fphar.2018.01425 Text en Copyright © 2018 Kolos, Voll, Bauder and Hausch. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Kolos, Jürgen M.
Voll, Andreas M.
Bauder, Michael
Hausch, Felix
FKBP Ligands—Where We Are and Where to Go?
title FKBP Ligands—Where We Are and Where to Go?
title_full FKBP Ligands—Where We Are and Where to Go?
title_fullStr FKBP Ligands—Where We Are and Where to Go?
title_full_unstemmed FKBP Ligands—Where We Are and Where to Go?
title_short FKBP Ligands—Where We Are and Where to Go?
title_sort fkbp ligands—where we are and where to go?
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290070/
https://www.ncbi.nlm.nih.gov/pubmed/30568592
http://dx.doi.org/10.3389/fphar.2018.01425
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