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Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor

Interferon (IFN)-τ secreted only by ruminant endometrium, helps in maternal recognition of pregnancy and exhibit antiviral and antiproliferative activity. Among different types of IFN-τ, IFN-τ1c and IFN- τ3a are the most highly expressed isoforms. In the present study structure of INF-τ1c was predic...

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Autores principales: Jamwal, Vishawdeep Singh, Modi, Gourav, George, Aman, Chauhan, Manmohan Singh
Formato: Texto
Lenguaje:English
Publicado: Biomedical Informatics Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825600/
https://www.ncbi.nlm.nih.gov/pubmed/20198192
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author Jamwal, Vishawdeep Singh
Modi, Gourav
George, Aman
Chauhan, Manmohan Singh
author_facet Jamwal, Vishawdeep Singh
Modi, Gourav
George, Aman
Chauhan, Manmohan Singh
author_sort Jamwal, Vishawdeep Singh
collection PubMed
description Interferon (IFN)-τ secreted only by ruminant endometrium, helps in maternal recognition of pregnancy and exhibit antiviral and antiproliferative activity. Among different types of IFN-τ, IFN-τ1c and IFN- τ3a are the most highly expressed isoforms. In the present study structure of INF-τ1c was predicted using homology modelling. The best model was selected based on overall stereo-chemical quality. The generated 3D structure of the Interferon-τ1c protein of Bos taurus was predicted using the ovine interferon-τ (PDB ID: 1B5L_A) as template. The structure comprises of 5 α helices separated by loop regions, which is similar to the one predicted for other IFNs. Molecular interactions of bovine IFN-τ1c with human interferon Type 1 receptor (IFNAR1) was explored in an attempt to predict human IFNAR1 binding sites of IFN-τ1c.
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spelling pubmed-28256002010-03-02 Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor Jamwal, Vishawdeep Singh Modi, Gourav George, Aman Chauhan, Manmohan Singh Bioinformation Hypothesis Interferon (IFN)-τ secreted only by ruminant endometrium, helps in maternal recognition of pregnancy and exhibit antiviral and antiproliferative activity. Among different types of IFN-τ, IFN-τ1c and IFN- τ3a are the most highly expressed isoforms. In the present study structure of INF-τ1c was predicted using homology modelling. The best model was selected based on overall stereo-chemical quality. The generated 3D structure of the Interferon-τ1c protein of Bos taurus was predicted using the ovine interferon-τ (PDB ID: 1B5L_A) as template. The structure comprises of 5 α helices separated by loop regions, which is similar to the one predicted for other IFNs. Molecular interactions of bovine IFN-τ1c with human interferon Type 1 receptor (IFNAR1) was explored in an attempt to predict human IFNAR1 binding sites of IFN-τ1c. Biomedical Informatics Publishing Group 2009-10-13 /pmc/articles/PMC2825600/ /pubmed/20198192 Text en © 2009 Biomedical Informatics Publishing Group This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Jamwal, Vishawdeep Singh
Modi, Gourav
George, Aman
Chauhan, Manmohan Singh
Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title_full Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title_fullStr Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title_full_unstemmed Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title_short Molecular interactions between Bos taurus interferon-τ1c and human type I interferon receptor
title_sort molecular interactions between bos taurus interferon-τ1c and human type i interferon receptor
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825600/
https://www.ncbi.nlm.nih.gov/pubmed/20198192
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