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SuperPain—a resource on pain-relieving compounds targeting ion channels
Pain is more than an unpleasant sensory experience associated with actual or potential tissue damage: it is the most common reason for physician consultation and often dramatically affects quality of life. The management of pain is often difficult and new targets are required for more effective and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964982/ https://www.ncbi.nlm.nih.gov/pubmed/24271391 http://dx.doi.org/10.1093/nar/gkt1176 |
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author | Gohlke, Björn O. Preissner, Robert Preissner, Saskia |
author_facet | Gohlke, Björn O. Preissner, Robert Preissner, Saskia |
author_sort | Gohlke, Björn O. |
collection | PubMed |
description | Pain is more than an unpleasant sensory experience associated with actual or potential tissue damage: it is the most common reason for physician consultation and often dramatically affects quality of life. The management of pain is often difficult and new targets are required for more effective and specific treatment. SuperPain (http://bioinformatics.charite.de/superpain/) is freely available database for pain-stimulating and pain-relieving compounds, which bind or potentially bind to ion channels that are involved in the transmission of pain signals to the central nervous system, such as TRPV1, TRPM8, TRPA1, TREK1, TRESK, hERG, ASIC, P2X and voltage-gated sodium channels. The database consists of ∼8700 ligands, which are characterized by experimentally measured binding affinities. Additionally, 100 000 putative ligands are included. Moreover, the database provides 3D structures of receptors and predicted ligand-binding poses. These binding poses and a structural classification scheme provide hints for the design of new analgesic compounds. A user-friendly graphical interface allows similarity searching, visualization of ligands docked into the receptor, etc. |
format | Online Article Text |
id | pubmed-3964982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39649822014-03-25 SuperPain—a resource on pain-relieving compounds targeting ion channels Gohlke, Björn O. Preissner, Robert Preissner, Saskia Nucleic Acids Res VI. Genomic variation, diseases and drugs Pain is more than an unpleasant sensory experience associated with actual or potential tissue damage: it is the most common reason for physician consultation and often dramatically affects quality of life. The management of pain is often difficult and new targets are required for more effective and specific treatment. SuperPain (http://bioinformatics.charite.de/superpain/) is freely available database for pain-stimulating and pain-relieving compounds, which bind or potentially bind to ion channels that are involved in the transmission of pain signals to the central nervous system, such as TRPV1, TRPM8, TRPA1, TREK1, TRESK, hERG, ASIC, P2X and voltage-gated sodium channels. The database consists of ∼8700 ligands, which are characterized by experimentally measured binding affinities. Additionally, 100 000 putative ligands are included. Moreover, the database provides 3D structures of receptors and predicted ligand-binding poses. These binding poses and a structural classification scheme provide hints for the design of new analgesic compounds. A user-friendly graphical interface allows similarity searching, visualization of ligands docked into the receptor, etc. Oxford University Press 2014-01-01 2013-11-22 /pmc/articles/PMC3964982/ /pubmed/24271391 http://dx.doi.org/10.1093/nar/gkt1176 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | VI. Genomic variation, diseases and drugs Gohlke, Björn O. Preissner, Robert Preissner, Saskia SuperPain—a resource on pain-relieving compounds targeting ion channels |
title | SuperPain—a resource on pain-relieving compounds targeting ion channels |
title_full | SuperPain—a resource on pain-relieving compounds targeting ion channels |
title_fullStr | SuperPain—a resource on pain-relieving compounds targeting ion channels |
title_full_unstemmed | SuperPain—a resource on pain-relieving compounds targeting ion channels |
title_short | SuperPain—a resource on pain-relieving compounds targeting ion channels |
title_sort | superpain—a resource on pain-relieving compounds targeting ion channels |
topic | VI. Genomic variation, diseases and drugs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964982/ https://www.ncbi.nlm.nih.gov/pubmed/24271391 http://dx.doi.org/10.1093/nar/gkt1176 |
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