Literature DB >> 21630291

PROCOS: computational analysis of protein-protein complexes.

Florian Fink1, Jochen Hochrein, Vincent Wolowski, Rainer Merkl, Wolfram Gronwald.   

Abstract

One of the main challenges in protein-protein docking is a meaningful evaluation of the many putative solutions. Here we present a program (PROCOS) that calculates a probability-like measure to be native for a given complex. In contrast to scores often used for analyzing complex structures, the calculated probabilities offer the advantage of providing a fixed range of expected values. This will allow, in principle, the comparison of models corresponding to different targets that were solved with the same algorithm. Judgments are based on distributions of properties derived from a large database of native and false complexes. For complex analysis PROCOS uses these property distributions of native and false complexes together with a support vector machine (SVM). PROCOS was compared to the established scoring schemes of ZRANK and DFIRE. Employing a set of experimentally solved native complexes, high probability values above 50% were obtained for 90% of these structures. Next, the performance of PROCOS was tested on the 40 binary targets of the Dockground decoy set, on 14 targets of the RosettaDock decoy set and on 9 targets that participated in the CAPRI scoring evaluation. Again the advantage of using a probability-based scoring system becomes apparent and a reasonable number of near native complexes was found within the top ranked complexes. In conclusion, a novel fully automated method is presented that allows the reliable evaluation of protein-protein complexes.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21630291     DOI: 10.1002/jcc.21837

Source DB:  PubMed          Journal:  J Comput Chem        ISSN: 0192-8651            Impact factor:   3.376


  9 in total

1.  Protein docking model evaluation by 3D deep convolutional neural networks.

Authors:  Xiao Wang; Genki Terashi; Charles W Christoffer; Mengmeng Zhu; Daisuke Kihara
Journal:  Bioinformatics       Date:  2020-04-01       Impact factor: 6.937

2.  Protein-protein interaction specificity is captured by contact preferences and interface composition.

Authors:  Francesca Nadalin; Alessandra Carbone
Journal:  Bioinformatics       Date:  2018-02-01       Impact factor: 6.937

3.  NPPD: A Protein-Protein Docking Scoring Function Based on Dyadic Differences in Networks of Hydrophobic and Hydrophilic Amino Acid Residues.

Authors:  Edward S C Shih; Ming-Jing Hwang
Journal:  Biology (Basel)       Date:  2015-03-24

4.  The scoring of poses in protein-protein docking: current capabilities and future directions.

Authors:  Iain H Moal; Mieczyslaw Torchala; Paul A Bates; Juan Fernández-Recio
Journal:  BMC Bioinformatics       Date:  2013-10-01       Impact factor: 3.169

5.  Disentangling constraints using viability evolution principles in integrative modeling of macromolecular assemblies.

Authors:  Giorgio Tamò; Andrea Maesani; Sylvain Träger; Matteo T Degiacomi; Dario Floreano; Matteo Dal Peraro
Journal:  Sci Rep       Date:  2017-03-22       Impact factor: 4.379

6.  A machine learning approach for ranking clusters of docked protein-protein complexes by pairwise cluster comparison.

Authors:  Erik Pfeiffenberger; Raphael A G Chaleil; Iain H Moal; Paul A Bates
Journal:  Proteins       Date:  2017-01-20

7.  iScore: a novel graph kernel-based function for scoring protein-protein docking models.

Authors:  Cunliang Geng; Yong Jung; Nicolas Renaud; Vasant Honavar; Alexandre M J J Bonvin; Li C Xue
Journal:  Bioinformatics       Date:  2020-01-01       Impact factor: 6.937

8.  Classification and prediction of protein-protein interaction interface using machine learning algorithm.

Authors:  Subhrangshu Das; Saikat Chakrabarti
Journal:  Sci Rep       Date:  2021-01-19       Impact factor: 4.379

9.  Protein Docking Model Evaluation by Graph Neural Networks.

Authors:  Xiao Wang; Sean T Flannery; Daisuke Kihara
Journal:  Front Mol Biosci       Date:  2021-05-25
  9 in total

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