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Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains

Several proteins other than the frizzled receptors (Fzd) and the secreted Frizzled-related proteins (sFRP) contain Fzd-type cysteine-rich domains (CRD). We have termed these domains “putative Fzd-type CRDs”, as the relevance of Wnt signalling in the majority of these is unknown; the RORs, an excepti...

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Autores principales: Agostino, Mark, Pohl, Sebastian Öther-Gee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747125/
https://www.ncbi.nlm.nih.gov/pubmed/31454915
http://dx.doi.org/10.3390/ijms20174168
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author Agostino, Mark
Pohl, Sebastian Öther-Gee
author_facet Agostino, Mark
Pohl, Sebastian Öther-Gee
author_sort Agostino, Mark
collection PubMed
description Several proteins other than the frizzled receptors (Fzd) and the secreted Frizzled-related proteins (sFRP) contain Fzd-type cysteine-rich domains (CRD). We have termed these domains “putative Fzd-type CRDs”, as the relevance of Wnt signalling in the majority of these is unknown; the RORs, an exception to this, are well known for mediating non-canonical Wnt signalling. In this study, we have predicted the likely binding affinity of all Wnts for all putative Fzd-type CRDs. We applied both our previously determined Wnt‒Fzd CRD binding affinity prediction model, as well as a newly devised model wherein the lipid term was forced to contribute favourably to the predicted binding energy. The results obtained from our new model indicate that certain putative Fzd CRDs are much more likely to bind Wnts, in some cases exhibiting selectivity for specific Wnts. The results of this study inform the investigation of Wnt signalling modulation beyond Fzds and sFRPs.
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spelling pubmed-67471252019-09-27 Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains Agostino, Mark Pohl, Sebastian Öther-Gee Int J Mol Sci Article Several proteins other than the frizzled receptors (Fzd) and the secreted Frizzled-related proteins (sFRP) contain Fzd-type cysteine-rich domains (CRD). We have termed these domains “putative Fzd-type CRDs”, as the relevance of Wnt signalling in the majority of these is unknown; the RORs, an exception to this, are well known for mediating non-canonical Wnt signalling. In this study, we have predicted the likely binding affinity of all Wnts for all putative Fzd-type CRDs. We applied both our previously determined Wnt‒Fzd CRD binding affinity prediction model, as well as a newly devised model wherein the lipid term was forced to contribute favourably to the predicted binding energy. The results obtained from our new model indicate that certain putative Fzd CRDs are much more likely to bind Wnts, in some cases exhibiting selectivity for specific Wnts. The results of this study inform the investigation of Wnt signalling modulation beyond Fzds and sFRPs. MDPI 2019-08-26 /pmc/articles/PMC6747125/ /pubmed/31454915 http://dx.doi.org/10.3390/ijms20174168 Text en © 2019 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 Article
Agostino, Mark
Pohl, Sebastian Öther-Gee
Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title_full Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title_fullStr Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title_full_unstemmed Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title_short Wnt Binding Affinity Prediction for Putative Frizzled-Type Cysteine-Rich Domains
title_sort wnt binding affinity prediction for putative frizzled-type cysteine-rich domains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747125/
https://www.ncbi.nlm.nih.gov/pubmed/31454915
http://dx.doi.org/10.3390/ijms20174168
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