Literature DB >> 26608033

Structural in silico dissection of the collagen V interactome to identify genotype-phenotype correlations in classic Ehlers-Danlos Syndrome (EDS).

Lisanna Paladin1, Silvio C E Tosatto2, Giovanni Minervini3.   

Abstract

Collagen V mutations are associated with Elhers-Danlos syndrome (EDS), a group of heritable collagenopathies. Collagen V structure is not available and the disease-causing mechanism is unclear. To address this issue, we manually curated missense mutations suspected to promote classic type EDS (cEDS) insurgence from the literature and performed a genotype-phenotype correlation study. Further, we generated a homology model of the collagen V triple helix to evaluate the pathogenic effects. The resulting structure was used to map known protein-protein interactions enriched with in silico predictions. An interaction network model for collagen V was created. We found that cEDS heterogeneous manifestations may be explained by the involvement in two different extracellular matrix pathways, related to cell adhesion and tissue repair or cell differentiation, growth and apoptosis.
Copyright © 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bioinformatics; Collagen V; Collagenopathies; Ehlers–Danlos Syndrome

Mesh:

Substances:

Year:  2015        PMID: 26608033     DOI: 10.1016/j.febslet.2015.11.022

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  5 in total

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Journal:  Cell Rep       Date:  2020-07-07       Impact factor: 9.423

2.  New variants in COL5A1 gene among Polish patients with Ehlers-Danlos syndrome: analysis of nine cases.

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3.  Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by synonymous mutation in COL5A2.

Authors:  Na Ma; Zhenhua Zhu; Jing Liu; Ying Peng; Xiaomeng Zhao; Weiling Tang; Zhengjun Jia; Hui Xi; Bodi Gao; Hua Wang; Juan Du
Journal:  Mol Genet Genomic Med       Date:  2021-04-08       Impact factor: 2.183

4.  A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia.

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  5 in total

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