Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.

Computational prediction of residues that participate in protein-protein interactions is a difficult task, and state of the art methods have shown only limited success in this arena. One possible problem with these methods is that they try to predict interacting residues without incorporating inform...

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Main Authors: Shandar Ahmad, Kenji Mizuguchi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22194998/pdf/?tool=EBI
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spelling doaj-50c7f09e77ce4581ad20f6acaaba44b22021-03-04T01:15:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01612e2910410.1371/journal.pone.0029104Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.Shandar AhmadKenji MizuguchiComputational prediction of residues that participate in protein-protein interactions is a difficult task, and state of the art methods have shown only limited success in this arena. One possible problem with these methods is that they try to predict interacting residues without incorporating information about the partner protein, although it is unclear how much partner information could enhance prediction performance. To address this issue, the two following comparisons are of crucial significance: (a) comparison between the predictability of inter-protein residue pairs, i.e., predicting exactly which residue pairs interact with each other given two protein sequences; this can be achieved by either combining conventional single-protein predictions or making predictions using a new model trained directly on the residue pairs, and the performance of these two approaches may be compared: (b) comparison between the predictability of the interacting residues in a single protein (irrespective of the partner residue or protein) from conventional methods and predictions converted from the pair-wise trained model. Using these two streams of training and validation procedures and employing similar two-stage neural networks, we showed that the models trained on pair-wise contacts outperformed the partner-unaware models in predicting both interacting pairs and interacting single-protein residues. Prediction performance decreased with the size of the conformational change upon complex formation; this trend is similar to docking, even though no structural information was used in our prediction. An example application that predicts two partner-specific interfaces of a protein was shown to be effective, highlighting the potential of the proposed approach. Finally, a preliminary attempt was made to score docking decoy poses using prediction of interacting residue pairs; this analysis produced an encouraging result.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22194998/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Shandar Ahmad
Kenji Mizuguchi
spellingShingle Shandar Ahmad
Kenji Mizuguchi
Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
PLoS ONE
author_facet Shandar Ahmad
Kenji Mizuguchi
author_sort Shandar Ahmad
title Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
title_short Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
title_full Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
title_fullStr Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
title_full_unstemmed Partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
title_sort partner-aware prediction of interacting residues in protein-protein complexes from sequence data.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Computational prediction of residues that participate in protein-protein interactions is a difficult task, and state of the art methods have shown only limited success in this arena. One possible problem with these methods is that they try to predict interacting residues without incorporating information about the partner protein, although it is unclear how much partner information could enhance prediction performance. To address this issue, the two following comparisons are of crucial significance: (a) comparison between the predictability of inter-protein residue pairs, i.e., predicting exactly which residue pairs interact with each other given two protein sequences; this can be achieved by either combining conventional single-protein predictions or making predictions using a new model trained directly on the residue pairs, and the performance of these two approaches may be compared: (b) comparison between the predictability of the interacting residues in a single protein (irrespective of the partner residue or protein) from conventional methods and predictions converted from the pair-wise trained model. Using these two streams of training and validation procedures and employing similar two-stage neural networks, we showed that the models trained on pair-wise contacts outperformed the partner-unaware models in predicting both interacting pairs and interacting single-protein residues. Prediction performance decreased with the size of the conformational change upon complex formation; this trend is similar to docking, even though no structural information was used in our prediction. An example application that predicts two partner-specific interfaces of a protein was shown to be effective, highlighting the potential of the proposed approach. Finally, a preliminary attempt was made to score docking decoy poses using prediction of interacting residue pairs; this analysis produced an encouraging result.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22194998/pdf/?tool=EBI
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