Improved contact predictions using the recognition of protein like contact patterns.
Given sufficient large protein families, and using a global statistical inference approach, it is possible to obtain sufficient accuracy in protein residue contact predictions to predict the structure of many proteins. However, these approaches do not consider the fact that the contacts in a protein...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2014-11-01
|
Series: | PLoS Computational Biology |
Online Access: | http://europepmc.org/articles/PMC4222596?pdf=render |
id |
doaj-bf3ee7bc23c24adf947d0a973eb0912b |
---|---|
record_format |
Article |
spelling |
doaj-bf3ee7bc23c24adf947d0a973eb0912b2020-11-24T21:51:04ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582014-11-011011e100388910.1371/journal.pcbi.1003889Improved contact predictions using the recognition of protein like contact patterns.Marcin J SkwarkDaniele RaimondiMirco MichelArne ElofssonGiven sufficient large protein families, and using a global statistical inference approach, it is possible to obtain sufficient accuracy in protein residue contact predictions to predict the structure of many proteins. However, these approaches do not consider the fact that the contacts in a protein are neither randomly, nor independently distributed, but actually follow precise rules governed by the structure of the protein and thus are interdependent. Here, we present PconsC2, a novel method that uses a deep learning approach to identify protein-like contact patterns to improve contact predictions. A substantial enhancement can be seen for all contacts independently on the number of aligned sequences, residue separation or secondary structure type, but is largest for β-sheet containing proteins. In addition to being superior to earlier methods based on statistical inferences, in comparison to state of the art methods using machine learning, PconsC2 is superior for families with more than 100 effective sequence homologs. The improved contact prediction enables improved structure prediction.http://europepmc.org/articles/PMC4222596?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marcin J Skwark Daniele Raimondi Mirco Michel Arne Elofsson |
spellingShingle |
Marcin J Skwark Daniele Raimondi Mirco Michel Arne Elofsson Improved contact predictions using the recognition of protein like contact patterns. PLoS Computational Biology |
author_facet |
Marcin J Skwark Daniele Raimondi Mirco Michel Arne Elofsson |
author_sort |
Marcin J Skwark |
title |
Improved contact predictions using the recognition of protein like contact patterns. |
title_short |
Improved contact predictions using the recognition of protein like contact patterns. |
title_full |
Improved contact predictions using the recognition of protein like contact patterns. |
title_fullStr |
Improved contact predictions using the recognition of protein like contact patterns. |
title_full_unstemmed |
Improved contact predictions using the recognition of protein like contact patterns. |
title_sort |
improved contact predictions using the recognition of protein like contact patterns. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Computational Biology |
issn |
1553-734X 1553-7358 |
publishDate |
2014-11-01 |
description |
Given sufficient large protein families, and using a global statistical inference approach, it is possible to obtain sufficient accuracy in protein residue contact predictions to predict the structure of many proteins. However, these approaches do not consider the fact that the contacts in a protein are neither randomly, nor independently distributed, but actually follow precise rules governed by the structure of the protein and thus are interdependent. Here, we present PconsC2, a novel method that uses a deep learning approach to identify protein-like contact patterns to improve contact predictions. A substantial enhancement can be seen for all contacts independently on the number of aligned sequences, residue separation or secondary structure type, but is largest for β-sheet containing proteins. In addition to being superior to earlier methods based on statistical inferences, in comparison to state of the art methods using machine learning, PconsC2 is superior for families with more than 100 effective sequence homologs. The improved contact prediction enables improved structure prediction. |
url |
http://europepmc.org/articles/PMC4222596?pdf=render |
work_keys_str_mv |
AT marcinjskwark improvedcontactpredictionsusingtherecognitionofproteinlikecontactpatterns AT danieleraimondi improvedcontactpredictionsusingtherecognitionofproteinlikecontactpatterns AT mircomichel improvedcontactpredictionsusingtherecognitionofproteinlikecontactpatterns AT arneelofsson improvedcontactpredictionsusingtherecognitionofproteinlikecontactpatterns |
_version_ |
1725880701053566976 |