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Identification of hot spot residues at protein-protein interface
It is known that binding free energy of protein-protein interaction is mainly contributed by hot spot (high energy) interface residues. Here, we investigate the characteristics of hot spots by examining inter-atomic sidechain-sidechain interactions using a dataset of 296 alanine-mutated interface re...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics Publishing Group
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891667/ https://www.ncbi.nlm.nih.gov/pubmed/17597870 |
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author | Li, Lei Zhao, Bing Cui, Zhanhua Gan, Jacob Sakharkar, Meena Kishore Kangueane, Pandjassarame |
author_facet | Li, Lei Zhao, Bing Cui, Zhanhua Gan, Jacob Sakharkar, Meena Kishore Kangueane, Pandjassarame |
author_sort | Li, Lei |
collection | PubMed |
description | It is known that binding free energy of protein-protein interaction is mainly contributed by hot spot (high energy) interface residues. Here, we investigate the characteristics of hot spots by examining inter-atomic sidechain-sidechain interactions using a dataset of 296 alanine-mutated interface residues. Results show that hot spots participate in strong and energetically favorable sidechain-sidechain interactions. Subsequently, we describe a novel, yet simple ‘hot spot’ prediction model with an accuracy that is similar to many available approaches. The model is also shown to efficiently distinguish specific protein-protein interactions from non-specific interactions. |
format | Text |
id | pubmed-1891667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Biomedical Informatics Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-18916672007-06-27 Identification of hot spot residues at protein-protein interface Li, Lei Zhao, Bing Cui, Zhanhua Gan, Jacob Sakharkar, Meena Kishore Kangueane, Pandjassarame Bioinformation Hypothesis It is known that binding free energy of protein-protein interaction is mainly contributed by hot spot (high energy) interface residues. Here, we investigate the characteristics of hot spots by examining inter-atomic sidechain-sidechain interactions using a dataset of 296 alanine-mutated interface residues. Results show that hot spots participate in strong and energetically favorable sidechain-sidechain interactions. Subsequently, we describe a novel, yet simple ‘hot spot’ prediction model with an accuracy that is similar to many available approaches. The model is also shown to efficiently distinguish specific protein-protein interactions from non-specific interactions. Biomedical Informatics Publishing Group 2006-04-04 /pmc/articles/PMC1891667/ /pubmed/17597870 Text en © 2006 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 Li, Lei Zhao, Bing Cui, Zhanhua Gan, Jacob Sakharkar, Meena Kishore Kangueane, Pandjassarame Identification of hot spot residues at protein-protein interface |
title | Identification of hot spot residues at protein-protein interface |
title_full | Identification of hot spot residues at protein-protein interface |
title_fullStr | Identification of hot spot residues at protein-protein interface |
title_full_unstemmed | Identification of hot spot residues at protein-protein interface |
title_short | Identification of hot spot residues at protein-protein interface |
title_sort | identification of hot spot residues at protein-protein interface |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891667/ https://www.ncbi.nlm.nih.gov/pubmed/17597870 |
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