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Highlighting membrane protein structure and function: A celebration of the Protein Data Bank
Biological membranes define the boundaries of cells and compartmentalize the chemical and physical processes required for life. Many biological processes are carried out by proteins embedded in or associated with such membranes. Determination of membrane protein (MP) structures at atomic or near-ato...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102919/ https://www.ncbi.nlm.nih.gov/pubmed/33744283 http://dx.doi.org/10.1016/j.jbc.2021.100557 |
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author | Li, Fei Egea, Pascal F. Vecchio, Alex J. Asial, Ignacio Gupta, Meghna Paulino, Joana Bajaj, Ruchika Dickinson, Miles Sasha Ferguson-Miller, Shelagh Monk, Brian C. Stroud, Robert M. |
author_facet | Li, Fei Egea, Pascal F. Vecchio, Alex J. Asial, Ignacio Gupta, Meghna Paulino, Joana Bajaj, Ruchika Dickinson, Miles Sasha Ferguson-Miller, Shelagh Monk, Brian C. Stroud, Robert M. |
author_sort | Li, Fei |
collection | PubMed |
description | Biological membranes define the boundaries of cells and compartmentalize the chemical and physical processes required for life. Many biological processes are carried out by proteins embedded in or associated with such membranes. Determination of membrane protein (MP) structures at atomic or near-atomic resolution plays a vital role in elucidating their structural and functional impact in biology. This endeavor has determined 1198 unique MP structures as of early 2021. The value of these structures is expanded greatly by deposition of their three-dimensional (3D) coordinates into the Protein Data Bank (PDB) after the first atomic MP structure was elucidated in 1985. Since then, free access to MP structures facilitates broader and deeper understanding of MPs, which provides crucial new insights into their biological functions. Here we highlight the structural and functional biology of representative MPs and landmarks in the evolution of new technologies, with insights into key developments influenced by the PDB in magnifying their impact. |
format | Online Article Text |
id | pubmed-8102919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81029192021-05-14 Highlighting membrane protein structure and function: A celebration of the Protein Data Bank Li, Fei Egea, Pascal F. Vecchio, Alex J. Asial, Ignacio Gupta, Meghna Paulino, Joana Bajaj, Ruchika Dickinson, Miles Sasha Ferguson-Miller, Shelagh Monk, Brian C. Stroud, Robert M. J Biol Chem JBC Reviews Biological membranes define the boundaries of cells and compartmentalize the chemical and physical processes required for life. Many biological processes are carried out by proteins embedded in or associated with such membranes. Determination of membrane protein (MP) structures at atomic or near-atomic resolution plays a vital role in elucidating their structural and functional impact in biology. This endeavor has determined 1198 unique MP structures as of early 2021. The value of these structures is expanded greatly by deposition of their three-dimensional (3D) coordinates into the Protein Data Bank (PDB) after the first atomic MP structure was elucidated in 1985. Since then, free access to MP structures facilitates broader and deeper understanding of MPs, which provides crucial new insights into their biological functions. Here we highlight the structural and functional biology of representative MPs and landmarks in the evolution of new technologies, with insights into key developments influenced by the PDB in magnifying their impact. American Society for Biochemistry and Molecular Biology 2021-03-18 /pmc/articles/PMC8102919/ /pubmed/33744283 http://dx.doi.org/10.1016/j.jbc.2021.100557 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | JBC Reviews Li, Fei Egea, Pascal F. Vecchio, Alex J. Asial, Ignacio Gupta, Meghna Paulino, Joana Bajaj, Ruchika Dickinson, Miles Sasha Ferguson-Miller, Shelagh Monk, Brian C. Stroud, Robert M. Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title | Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title_full | Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title_fullStr | Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title_full_unstemmed | Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title_short | Highlighting membrane protein structure and function: A celebration of the Protein Data Bank |
title_sort | highlighting membrane protein structure and function: a celebration of the protein data bank |
topic | JBC Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102919/ https://www.ncbi.nlm.nih.gov/pubmed/33744283 http://dx.doi.org/10.1016/j.jbc.2021.100557 |
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