Literature DB >> 21465136

Sequence conservation in the prediction of catalytic sites.

Yongchao Dou1, Xingbo Geng, Hongyun Gao, Jialiang Yang, Xiaoqi Zheng, Jun Wang.   

Abstract

Predicting catalytic sites of a given enzyme is an important open problem of Bioinformatics. Recently, many machine learning-based methods have been developed which have the advantage that they can account for many sequential or structural features. We found that although many kinds of features are incorporated, protein sequence conservation is the main part of information they used and should play an important role in the future. So we tested several conservation features in their ability to predict catalytic sites by using the Support Vector Machine classifier. Our results suggest that position specific scoring matrix performs better than other features and incorporating conservation information of sequentially adjacent sites is more effective than that of structurally adjacent ones. Moreover, although conservation information is effective in predicting catalytic sites, it is a difficult problem to optimize the combination of conservation features and other ones.

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Year:  2011        PMID: 21465136     DOI: 10.1007/s10930-011-9324-2

Source DB:  PubMed          Journal:  Protein J        ISSN: 1572-3887            Impact factor:   2.371


  36 in total

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Authors:  Fredrik Johansson; Hiroyuki Toh
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3.  An improved prediction of catalytic residues in enzyme structures.

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Journal:  Protein Eng Des Sel       Date:  2008-02-20       Impact factor: 1.650

4.  Prediction of protein functional residues from sequence by probability density estimation.

Authors:  J D Fischer; C E Mayer; J Söding
Journal:  Bioinformatics       Date:  2008-01-02       Impact factor: 6.937

5.  Robustness of the residue conservation score reflecting both frequencies and physicochemistries.

Authors:  X-S Liu; W-L Guo
Journal:  Amino Acids       Date:  2008-01-04       Impact factor: 3.520

6.  Improving position-specific predictions of protein functional sites using phylogenetic motifs.

Authors:  Bahadur K C Dukka; Dennis R Livesay
Journal:  Bioinformatics       Date:  2008-08-21       Impact factor: 6.937

7.  Several appropriate background distributions for entropy-based protein sequence conservation measures.

Authors:  Yongchao Dou; Xiaoqi Zheng; Jun Wang
Journal:  J Theor Biol       Date:  2009-10-04       Impact factor: 2.691

8.  Incorporating background frequency improves entropy-based residue conservation measures.

Authors:  Kai Wang; Ram Samudrala
Journal:  BMC Bioinformatics       Date:  2006-08-17       Impact factor: 3.169

9.  Active site prediction using evolutionary and structural information.

Authors:  Sriram Sankararaman; Fei Sha; Jack F Kirsch; Michael I Jordan; Kimmen Sjölander
Journal:  Bioinformatics       Date:  2010-01-14       Impact factor: 6.937

10.  Estimating residue evolutionary conservation by introducing von Neumann entropy and a novel gap-treating approach.

Authors:  S-W Zhang; Y-L Zhang; Q Pan; Y-M Cheng; K-C Chou
Journal:  Amino Acids       Date:  2007-08-21       Impact factor: 3.520

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  3 in total

1.  iCataly-PseAAC: Identification of Enzymes Catalytic Sites Using Sequence Evolution Information with Grey Model GM (2,1).

Authors:  Xuan Xiao; Meng-Juan Hui; Zi Liu; Wang-Ren Qiu
Journal:  J Membr Biol       Date:  2015-06-16       Impact factor: 1.843

2.  CLIPS-1D: analysis of multiple sequence alignments to deduce for residue-positions a role in catalysis, ligand-binding, or protein structure.

Authors:  Jan-Oliver Janda; Markus Busch; Fabian Kück; Mikhail Porfenenko; Rainer Merkl
Journal:  BMC Bioinformatics       Date:  2012-04-05       Impact factor: 3.169

3.  A new bioinformatics approach to natural protein collections: permutation structure contrasts of viral and cellular systems.

Authors:  Daniel J Graham
Journal:  Protein J       Date:  2013-04       Impact factor: 4.000

  3 in total

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