ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information
Abstract The formation of a stable complex between proteins lies at the core of a wide variety of biological processes and has been the focus of countless experiments. The huge amount of information contained in the protein structural interactome in the Protein Data Bank can now be used to character...
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2024
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Online Access: | https://doi.org/10.1038/s42003-023-05718-w https://doaj.org/article/c0e738ae06f14b90a8e16af6ae031f55 |
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ftdoajarticles:oai:doaj.org/article:c0e738ae06f14b90a8e16af6ae031f55 2024-02-11T10:00:41+01:00 ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information Marco Giulini Rodrigo V. Honorato Jesús L. Rivera Alexandre M. J. J. Bonvin 2024-01-01T00:00:00Z https://doi.org/10.1038/s42003-023-05718-w https://doaj.org/article/c0e738ae06f14b90a8e16af6ae031f55 EN eng Nature Portfolio https://doi.org/10.1038/s42003-023-05718-w https://doaj.org/toc/2399-3642 doi:10.1038/s42003-023-05718-w 2399-3642 https://doaj.org/article/c0e738ae06f14b90a8e16af6ae031f55 Communications Biology, Vol 7, Iss 1, Pp 1-9 (2024) Biology (General) QH301-705.5 article 2024 ftdoajarticles https://doi.org/10.1038/s42003-023-05718-w 2024-01-14T01:51:52Z Abstract The formation of a stable complex between proteins lies at the core of a wide variety of biological processes and has been the focus of countless experiments. The huge amount of information contained in the protein structural interactome in the Protein Data Bank can now be used to characterise and classify the existing biological interfaces. We here introduce ARCTIC-3D, a fast and user-friendly data mining and clustering software to retrieve data and rationalise the interface information associated with the protein input data. We demonstrate its use by various examples ranging from showing the increased interaction complexity of eukaryotic proteins, 20% of which on average have more than 3 different interfaces compared to only 10% for prokaryotes, to associating different functions to different interfaces. In the context of modelling biomolecular assemblies, we introduce the concept of “recognition entropy”, related to the number of possible interfaces of the components of a protein-protein complex, which we demonstrate to correlate with the modelling difficulty in classical docking approaches. The identified interface clusters can also be used to generate various combinations of interface-specific restraints for integrative modelling. The ARCTIC-3D software is freely available at github.com/haddocking/arctic3d and can be accessed as a web-service at wenmr.science.uu.nl/arctic3d. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Communications Biology 7 1 |
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Open Polar |
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Directory of Open Access Journals: DOAJ Articles |
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ftdoajarticles |
language |
English |
topic |
Biology (General) QH301-705.5 |
spellingShingle |
Biology (General) QH301-705.5 Marco Giulini Rodrigo V. Honorato Jesús L. Rivera Alexandre M. J. J. Bonvin ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
topic_facet |
Biology (General) QH301-705.5 |
description |
Abstract The formation of a stable complex between proteins lies at the core of a wide variety of biological processes and has been the focus of countless experiments. The huge amount of information contained in the protein structural interactome in the Protein Data Bank can now be used to characterise and classify the existing biological interfaces. We here introduce ARCTIC-3D, a fast and user-friendly data mining and clustering software to retrieve data and rationalise the interface information associated with the protein input data. We demonstrate its use by various examples ranging from showing the increased interaction complexity of eukaryotic proteins, 20% of which on average have more than 3 different interfaces compared to only 10% for prokaryotes, to associating different functions to different interfaces. In the context of modelling biomolecular assemblies, we introduce the concept of “recognition entropy”, related to the number of possible interfaces of the components of a protein-protein complex, which we demonstrate to correlate with the modelling difficulty in classical docking approaches. The identified interface clusters can also be used to generate various combinations of interface-specific restraints for integrative modelling. The ARCTIC-3D software is freely available at github.com/haddocking/arctic3d and can be accessed as a web-service at wenmr.science.uu.nl/arctic3d. |
format |
Article in Journal/Newspaper |
author |
Marco Giulini Rodrigo V. Honorato Jesús L. Rivera Alexandre M. J. J. Bonvin |
author_facet |
Marco Giulini Rodrigo V. Honorato Jesús L. Rivera Alexandre M. J. J. Bonvin |
author_sort |
Marco Giulini |
title |
ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
title_short |
ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
title_full |
ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
title_fullStr |
ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
title_full_unstemmed |
ARCTIC-3D: automatic retrieval and clustering of interfaces in complexes from 3D structural information |
title_sort |
arctic-3d: automatic retrieval and clustering of interfaces in complexes from 3d structural information |
publisher |
Nature Portfolio |
publishDate |
2024 |
url |
https://doi.org/10.1038/s42003-023-05718-w https://doaj.org/article/c0e738ae06f14b90a8e16af6ae031f55 |
geographic |
Arctic |
geographic_facet |
Arctic |
genre |
Arctic |
genre_facet |
Arctic |
op_source |
Communications Biology, Vol 7, Iss 1, Pp 1-9 (2024) |
op_relation |
https://doi.org/10.1038/s42003-023-05718-w https://doaj.org/toc/2399-3642 doi:10.1038/s42003-023-05718-w 2399-3642 https://doaj.org/article/c0e738ae06f14b90a8e16af6ae031f55 |
op_doi |
https://doi.org/10.1038/s42003-023-05718-w |
container_title |
Communications Biology |
container_volume |
7 |
container_issue |
1 |
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1790596389558812672 |