Literature DB >> 17109407

MUPRED: a tool for bridging the gap between template based methods and sequence profile based methods for protein secondary structure prediction.

Rajkumar Bondugula1, Dong Xu.   

Abstract

Predicting secondary structures from a protein sequence is an important step for characterizing the structural properties of a protein. Existing methods for protein secondary structure prediction can be broadly classified into template based or sequence profile based methods. We propose a novel framework that bridges the gap between the two fundamentally different approaches. Our framework integrates the information from the fuzzy k-nearest neighbor algorithm and position-specific scoring matrices using a neural network. It combines the strengths of the two methods and has a better potential to use the information in both the sequence and structure databases than existing methods. We implemented the framework into a software system MUPRED. MUPRED has achieved three-state prediction accuracy (Q3) ranging from 79.2 to 80.14%, depending on which benchmark dataset is used. A higher Q3 can be achieved if a query protein has a significant sequence identity (>25%) to a template in PDB. MUPRED also estimates the prediction accuracy at the individual residue level more quantitatively than existing methods. The MUPRED web server and executables are freely available at http://digbio.missouri.edu/mupred. 2006 Wiley-Liss, Inc.

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Year:  2007        PMID: 17109407     DOI: 10.1002/prot.21177

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  13 in total

1.  Combining sequence and structural profiles for protein solvent accessibility prediction.

Authors:  Rajkumar Bondugula; Dong Xu
Journal:  Comput Syst Bioinformatics Conf       Date:  2008

Review 2.  From local structure to a global framework: recognition of protein folds.

Authors:  Agnel Praveen Joseph; Alexandre G de Brevern
Journal:  J R Soc Interface       Date:  2014-04-16       Impact factor: 4.118

3.  SPINE X: improving protein secondary structure prediction by multistep learning coupled with prediction of solvent accessible surface area and backbone torsion angles.

Authors:  Eshel Faraggi; Tuo Zhang; Yuedong Yang; Lukasz Kurgan; Yaoqi Zhou
Journal:  J Comput Chem       Date:  2011-11-02       Impact factor: 3.376

4.  MUFOLD: A new solution for protein 3D structure prediction.

Authors:  Jingfen Zhang; Qingguo Wang; Bogdan Barz; Zhiquan He; Ioan Kosztin; Yi Shang; Dong Xu
Journal:  Proteins       Date:  2010-04

Review 5.  Template-based protein modeling: recent methodological advances.

Authors:  Pankaj R Daga; Ronak Y Patel; Robert J Doerksen
Journal:  Curr Top Med Chem       Date:  2010       Impact factor: 3.295

6.  Improving protein secondary structure prediction based on short subsequences with local structure similarity.

Authors:  Hsin-Nan Lin; Ting-Yi Sung; Shinn-Ying Ho; Wen-Lian Hsu
Journal:  BMC Genomics       Date:  2010-12-02       Impact factor: 3.969

7.  Profiles and majority voting-based ensemble method for protein secondary structure prediction.

Authors:  Hafida Bouziane; Belhadri Messabih; Abdallah Chouarfia
Journal:  Evol Bioinform Online       Date:  2011-10-10       Impact factor: 1.625

8.  Improving prediction of secondary structure, local backbone angles, and solvent accessible surface area of proteins by iterative deep learning.

Authors:  Rhys Heffernan; Kuldip Paliwal; James Lyons; Abdollah Dehzangi; Alok Sharma; Jihua Wang; Abdul Sattar; Yuedong Yang; Yaoqi Zhou
Journal:  Sci Rep       Date:  2015-06-22       Impact factor: 4.379

9.  PSPP: a protein structure prediction pipeline for computing clusters.

Authors:  Michael S Lee; Rajkumar Bondugula; Valmik Desai; Nela Zavaljevski; In-Chul Yeh; Anders Wallqvist; Jaques Reifman
Journal:  PLoS One       Date:  2009-07-16       Impact factor: 3.240

10.  FIEFDom: a transparent domain boundary recognition system using a fuzzy mean operator.

Authors:  Rajkumar Bondugula; Michael S Lee; Anders Wallqvist
Journal:  Nucleic Acids Res       Date:  2008-12-04       Impact factor: 16.971

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