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Proteins Binding to the Carbohydrate HNK-1: Common Origins?
The human natural killer (HNK-1) carbohydrate plays important roles during nervous system development, regeneration after trauma and synaptic plasticity. Four proteins have been identified as receptors for HNK-1: the laminin adhesion molecule, high-mobility group box 1 and 2 (also called amphoterin)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347730/ https://www.ncbi.nlm.nih.gov/pubmed/34360882 http://dx.doi.org/10.3390/ijms22158116 |
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author | Castillo, Gaston Kleene, Ralf Schachner, Melitta Loers, Gabriele Torda, Andrew E. |
author_facet | Castillo, Gaston Kleene, Ralf Schachner, Melitta Loers, Gabriele Torda, Andrew E. |
author_sort | Castillo, Gaston |
collection | PubMed |
description | The human natural killer (HNK-1) carbohydrate plays important roles during nervous system development, regeneration after trauma and synaptic plasticity. Four proteins have been identified as receptors for HNK-1: the laminin adhesion molecule, high-mobility group box 1 and 2 (also called amphoterin) and cadherin 2 (also called N-cadherin). Because of HNK-1′s importance, we asked whether additional receptors for HNK-1 exist and whether the four identified proteins share any similarity in their primary structures. A set of 40,000 sequences homologous to the known HNK-1 receptors was selected and used for large-scale sequence alignments and motif searches. Although there are conserved regions and highly conserved sites within each of these protein families, there was no sequence similarity or conserved sequence motifs found to be shared by all families. Since HNK-1 receptors have not been compared regarding binding constants and since it is not known whether the sulfated or non-sulfated part of HKN-1 represents the structurally crucial ligand, the receptors are more heterogeneous in primary structure than anticipated, possibly involving different receptor or ligand regions. We thus conclude that the primary protein structure may not be the sole determinant for a bona fide HNK-1 receptor, rendering receptor structure more complex than originally assumed. |
format | Online Article Text |
id | pubmed-8347730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83477302021-08-08 Proteins Binding to the Carbohydrate HNK-1: Common Origins? Castillo, Gaston Kleene, Ralf Schachner, Melitta Loers, Gabriele Torda, Andrew E. Int J Mol Sci Article The human natural killer (HNK-1) carbohydrate plays important roles during nervous system development, regeneration after trauma and synaptic plasticity. Four proteins have been identified as receptors for HNK-1: the laminin adhesion molecule, high-mobility group box 1 and 2 (also called amphoterin) and cadherin 2 (also called N-cadherin). Because of HNK-1′s importance, we asked whether additional receptors for HNK-1 exist and whether the four identified proteins share any similarity in their primary structures. A set of 40,000 sequences homologous to the known HNK-1 receptors was selected and used for large-scale sequence alignments and motif searches. Although there are conserved regions and highly conserved sites within each of these protein families, there was no sequence similarity or conserved sequence motifs found to be shared by all families. Since HNK-1 receptors have not been compared regarding binding constants and since it is not known whether the sulfated or non-sulfated part of HKN-1 represents the structurally crucial ligand, the receptors are more heterogeneous in primary structure than anticipated, possibly involving different receptor or ligand regions. We thus conclude that the primary protein structure may not be the sole determinant for a bona fide HNK-1 receptor, rendering receptor structure more complex than originally assumed. MDPI 2021-07-29 /pmc/articles/PMC8347730/ /pubmed/34360882 http://dx.doi.org/10.3390/ijms22158116 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Castillo, Gaston Kleene, Ralf Schachner, Melitta Loers, Gabriele Torda, Andrew E. Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title | Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title_full | Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title_fullStr | Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title_full_unstemmed | Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title_short | Proteins Binding to the Carbohydrate HNK-1: Common Origins? |
title_sort | proteins binding to the carbohydrate hnk-1: common origins? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347730/ https://www.ncbi.nlm.nih.gov/pubmed/34360882 http://dx.doi.org/10.3390/ijms22158116 |
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