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Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors
The enzyme geranylgeranyl diphosphate synthase (GGDPS) catalyzes the synthesis of the 20-carbon isoprenoid geranylgeranyl diphosphate (GGPP). GGPP is the isoprenoid donor for protein geranylgeranylation reactions catalyzed by the enzymes geranylgeranyl transferase (GGTase) I and II. Inhibitors of GG...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902023/ https://www.ncbi.nlm.nih.gov/pubmed/28555000 http://dx.doi.org/10.3390/molecules22060886 |
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author | Haney, Staci L. Wills, Veronica S. Wiemer, David F. Holstein, Sarah A. |
author_facet | Haney, Staci L. Wills, Veronica S. Wiemer, David F. Holstein, Sarah A. |
author_sort | Haney, Staci L. |
collection | PubMed |
description | The enzyme geranylgeranyl diphosphate synthase (GGDPS) catalyzes the synthesis of the 20-carbon isoprenoid geranylgeranyl diphosphate (GGPP). GGPP is the isoprenoid donor for protein geranylgeranylation reactions catalyzed by the enzymes geranylgeranyl transferase (GGTase) I and II. Inhibitors of GGDPS result in diminution of protein geranylgeranylation through depletion of cellular GGPP levels, and there has been interest in GGDPS inhibitors as potential anti-cancer agents. Here we discuss recent advances in the development of GGDPS inhibitors, including insights gained by structure-function relationships, and review the preclinical data that support the continued development of this novel class of drugs. |
format | Online Article Text |
id | pubmed-5902023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59020232018-04-16 Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors Haney, Staci L. Wills, Veronica S. Wiemer, David F. Holstein, Sarah A. Molecules Review The enzyme geranylgeranyl diphosphate synthase (GGDPS) catalyzes the synthesis of the 20-carbon isoprenoid geranylgeranyl diphosphate (GGPP). GGPP is the isoprenoid donor for protein geranylgeranylation reactions catalyzed by the enzymes geranylgeranyl transferase (GGTase) I and II. Inhibitors of GGDPS result in diminution of protein geranylgeranylation through depletion of cellular GGPP levels, and there has been interest in GGDPS inhibitors as potential anti-cancer agents. Here we discuss recent advances in the development of GGDPS inhibitors, including insights gained by structure-function relationships, and review the preclinical data that support the continued development of this novel class of drugs. MDPI 2017-05-27 /pmc/articles/PMC5902023/ /pubmed/28555000 http://dx.doi.org/10.3390/molecules22060886 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Haney, Staci L. Wills, Veronica S. Wiemer, David F. Holstein, Sarah A. Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title | Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title_full | Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title_fullStr | Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title_full_unstemmed | Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title_short | Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors |
title_sort | recent advances in the development of mammalian geranylgeranyl diphosphate synthase inhibitors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902023/ https://www.ncbi.nlm.nih.gov/pubmed/28555000 http://dx.doi.org/10.3390/molecules22060886 |
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