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3D Complex: A Structural Classification of Protein Complexes
Most of the proteins in a cell assemble into complexes to carry out their function. It is therefore crucial to understand the physicochemical properties as well as the evolution of interactions between proteins. The Protein Data Bank represents an important source of information for such studies, be...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636673/ https://www.ncbi.nlm.nih.gov/pubmed/17112313 http://dx.doi.org/10.1371/journal.pcbi.0020155 |
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author | Levy, Emmanuel D Pereira-Leal, Jose B Chothia, Cyrus Teichmann, Sarah A |
author_facet | Levy, Emmanuel D Pereira-Leal, Jose B Chothia, Cyrus Teichmann, Sarah A |
author_sort | Levy, Emmanuel D |
collection | PubMed |
description | Most of the proteins in a cell assemble into complexes to carry out their function. It is therefore crucial to understand the physicochemical properties as well as the evolution of interactions between proteins. The Protein Data Bank represents an important source of information for such studies, because more than half of the structures are homo- or heteromeric protein complexes. Here we propose the first hierarchical classification of whole protein complexes of known 3-D structure, based on representing their fundamental structural features as a graph. This classification provides the first overview of all the complexes in the Protein Data Bank and allows nonredundant sets to be derived at different levels of detail. This reveals that between one-half and two-thirds of known structures are multimeric, depending on the level of redundancy accepted. We also analyse the structures in terms of the topological arrangement of their subunits and find that they form a small number of arrangements compared with all theoretically possible ones. This is because most complexes contain four subunits or less, and the large majority are homomeric. In addition, there is a strong tendency for symmetry in complexes, even for heteromeric complexes. Finally, through comparison of Biological Units in the Protein Data Bank with the Protein Quaternary Structure database, we identified many possible errors in quaternary structure assignments. Our classification, available as a database and Web server at http://www.3Dcomplex.org, will be a starting point for future work aimed at understanding the structure and evolution of protein complexes. |
format | Text |
id | pubmed-1636673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-16366732006-11-17 3D Complex: A Structural Classification of Protein Complexes Levy, Emmanuel D Pereira-Leal, Jose B Chothia, Cyrus Teichmann, Sarah A PLoS Comput Biol Research Article Most of the proteins in a cell assemble into complexes to carry out their function. It is therefore crucial to understand the physicochemical properties as well as the evolution of interactions between proteins. The Protein Data Bank represents an important source of information for such studies, because more than half of the structures are homo- or heteromeric protein complexes. Here we propose the first hierarchical classification of whole protein complexes of known 3-D structure, based on representing their fundamental structural features as a graph. This classification provides the first overview of all the complexes in the Protein Data Bank and allows nonredundant sets to be derived at different levels of detail. This reveals that between one-half and two-thirds of known structures are multimeric, depending on the level of redundancy accepted. We also analyse the structures in terms of the topological arrangement of their subunits and find that they form a small number of arrangements compared with all theoretically possible ones. This is because most complexes contain four subunits or less, and the large majority are homomeric. In addition, there is a strong tendency for symmetry in complexes, even for heteromeric complexes. Finally, through comparison of Biological Units in the Protein Data Bank with the Protein Quaternary Structure database, we identified many possible errors in quaternary structure assignments. Our classification, available as a database and Web server at http://www.3Dcomplex.org, will be a starting point for future work aimed at understanding the structure and evolution of protein complexes. Public Library of Science 2006-11 2006-11-17 /pmc/articles/PMC1636673/ /pubmed/17112313 http://dx.doi.org/10.1371/journal.pcbi.0020155 Text en © 2006 Levy et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Levy, Emmanuel D Pereira-Leal, Jose B Chothia, Cyrus Teichmann, Sarah A 3D Complex: A Structural Classification of Protein Complexes |
title | 3D Complex: A Structural Classification of Protein Complexes |
title_full | 3D Complex: A Structural Classification of Protein Complexes |
title_fullStr | 3D Complex: A Structural Classification of Protein Complexes |
title_full_unstemmed | 3D Complex: A Structural Classification of Protein Complexes |
title_short | 3D Complex: A Structural Classification of Protein Complexes |
title_sort | 3d complex: a structural classification of protein complexes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636673/ https://www.ncbi.nlm.nih.gov/pubmed/17112313 http://dx.doi.org/10.1371/journal.pcbi.0020155 |
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