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Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein
A study recently published in hepatology communications provided insights into a variant of MTARC1 protein, which conveys protection against liver disease. Here, we report a crystal structure of the variant protein at near‐atomic resolution and compare it to the structure of the wildtype protein.[Im...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592780/ https://www.ncbi.nlm.nih.gov/pubmed/35560545 http://dx.doi.org/10.1002/hep4.1984 |
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author | Struwe, Michel A. Clement, Bernd Scheidig, Axel |
author_facet | Struwe, Michel A. Clement, Bernd Scheidig, Axel |
author_sort | Struwe, Michel A. |
collection | PubMed |
description | A study recently published in hepatology communications provided insights into a variant of MTARC1 protein, which conveys protection against liver disease. Here, we report a crystal structure of the variant protein at near‐atomic resolution and compare it to the structure of the wildtype protein.[Image: see text] |
format | Online Article Text |
id | pubmed-9592780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95927802022-10-26 Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein Struwe, Michel A. Clement, Bernd Scheidig, Axel Hepatol Commun Correspondence A study recently published in hepatology communications provided insights into a variant of MTARC1 protein, which conveys protection against liver disease. Here, we report a crystal structure of the variant protein at near‐atomic resolution and compare it to the structure of the wildtype protein.[Image: see text] John Wiley and Sons Inc. 2022-05-13 /pmc/articles/PMC9592780/ /pubmed/35560545 http://dx.doi.org/10.1002/hep4.1984 Text en © 2022 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Correspondence Struwe, Michel A. Clement, Bernd Scheidig, Axel Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title | Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title_full | Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title_fullStr | Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title_full_unstemmed | Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title_short | Letter to the editor: The clinically relevant MTARC1 p.Ala165Thr variant impacts neither the fold nor active site architecture of the human mARC1 protein |
title_sort | letter to the editor: the clinically relevant mtarc1 p.ala165thr variant impacts neither the fold nor active site architecture of the human marc1 protein |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592780/ https://www.ncbi.nlm.nih.gov/pubmed/35560545 http://dx.doi.org/10.1002/hep4.1984 |
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