Literature DB >> 33300029

MitImpact 3: modeling the residue interaction network of the Respiratory Chain subunits.

Stefano Castellana1, Tommaso Biagini1, Francesco Petrizzelli1,2, Luca Parca1, Noemi Panzironi2, Viviana Caputo2, Angelo Luigi Vescovi3, Massimo Carella4, Tommaso Mazza1.   

Abstract

Numerous lines of evidence have shown that the interaction between the nuclear and mitochondrial genomes ensures the efficient functioning of the OXPHOS complexes, with substantial implications in bioenergetics, adaptation, and disease. Their interaction is a fascinating and complex trait of the eukaryotic cell that MitImpact explores with its third major release. MitImpact expands its collection of genomic, clinical, and functional annotations of all non-synonymous substitutions of the human mitochondrial genome with new information on putative Compensated Pathogenic Deviations and co-varying amino acid sites of the Respiratory Chain subunits. It further provides evidence of energetic and structural residue compensation by techniques of molecular dynamics simulation. MitImpact is freely accessible at http://mitimpact.css-mendel.it.
© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

Entities:  

Year:  2021        PMID: 33300029      PMCID: PMC7779045          DOI: 10.1093/nar/gkaa1032

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  68 in total

1.  The Amber biomolecular simulation programs.

Authors:  David A Case; Thomas E Cheatham; Tom Darden; Holger Gohlke; Ray Luo; Kenneth M Merz; Alexey Onufriev; Carlos Simmerling; Bing Wang; Robert J Woods
Journal:  J Comput Chem       Date:  2005-12       Impact factor: 3.376

Review 2.  Structures of mitochondrial oxidative phosphorylation supercomplexes and mechanisms for their stabilisation.

Authors:  Yuriy Chaban; Egbert J Boekema; Natalya V Dudkina
Journal:  Biochim Biophys Acta       Date:  2013-10-30

3.  SNPdryad: predicting deleterious non-synonymous human SNPs using only orthologous protein sequences.

Authors:  Ka-Chun Wong; Zhaolei Zhang
Journal:  Bioinformatics       Date:  2014-01-02       Impact factor: 6.937

Review 4.  Mitochondrial DNA variation in human radiation and disease.

Authors:  Douglas C Wallace
Journal:  Cell       Date:  2015-09-24       Impact factor: 41.582

5.  Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.

Authors:  Tobias B Haack; Birgit Haberberger; Eva-Maria Frisch; Thomas Wieland; Arcangela Iuso; Matteo Gorza; Valentina Strecker; Elisabeth Graf; Johannes A Mayr; Ulrike Herberg; Julia B Hennermann; Thomas Klopstock; Klaus A Kuhn; Uwe Ahting; Wolfgang Sperl; Ekkehard Wilichowski; Georg F Hoffmann; Marketa Tesarova; Hana Hansikova; Jiri Zeman; Barbara Plecko; Massimo Zeviani; Ilka Wittig; Tim M Strom; Markus Schuelke; Peter Freisinger; Thomas Meitinger; Holger Prokisch
Journal:  J Med Genet       Date:  2012-04       Impact factor: 6.318

6.  I-COMS: Interprotein-COrrelated Mutations Server.

Authors:  Javier Iserte; Franco L Simonetti; Diego J Zea; Elin Teppa; Cristina Marino-Buslje
Journal:  Nucleic Acids Res       Date:  2015-06-01       Impact factor: 16.971

7.  High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE.

Authors:  Stefano Castellana; Caterina Fusilli; Gianluigi Mazzoccoli; Tommaso Biagini; Daniele Capocefalo; Massimo Carella; Angelo Luigi Vescovi; Tommaso Mazza
Journal:  PLoS Comput Biol       Date:  2017-06-22       Impact factor: 4.475

8.  SWISS-MODEL: homology modelling of protein structures and complexes.

Authors:  Andrew Waterhouse; Martino Bertoni; Stefan Bienert; Gabriel Studer; Gerardo Tauriello; Rafal Gumienny; Florian T Heer; Tjaart A P de Beer; Christine Rempfer; Lorenza Bordoli; Rosalba Lepore; Torsten Schwede
Journal:  Nucleic Acids Res       Date:  2018-07-02       Impact factor: 16.971

9.  Self-consistency test reveals systematic bias in programs for prediction change of stability upon mutation.

Authors:  Dinara R Usmanova; Natalya S Bogatyreva; Joan Ariño Bernad; Aleksandra A Eremina; Anastasiya A Gorshkova; German M Kanevskiy; Lyubov R Lonishin; Alexander V Meister; Alisa G Yakupova; Fyodor A Kondrashov; Dmitry N Ivankov
Journal:  Bioinformatics       Date:  2018-11-01       Impact factor: 6.937

10.  Disease-causing mutations in subunits of OXPHOS complex I affect certain physical interactions.

Authors:  Gilad Barshad; Nicol Zlotnikov-Poznianski; Lihi Gal; Maya Schuldiner; Dan Mishmar
Journal:  Sci Rep       Date:  2019-07-10       Impact factor: 4.379

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  4 in total

1.  Identification of Somatic Mitochondrial DNA Mutations, Heteroplasmy, and Increased Levels of Catenanes in Tumor Specimens Obtained from Three Endometrial Cancer Patients.

Authors:  Matthew J Young; Ravi Sachidanandam; Dale B Hales; Laurent Brard; Kathy Robinson; Md Mostafijur Rahman; Pabitra Khadka; Kathleen Groesch; Carolyn K J Young
Journal:  Life (Basel)       Date:  2022-04-09

2.  Compensatory epistasis explored by molecular dynamics simulations.

Authors:  Sérgio F Sousa; Luísa Azevedo; Catarina Serrano; Carla S S Teixeira; David N Cooper; João Carneiro; Mónica Lopes-Marques; Peter D Stenson; António Amorim; Maria J Prata
Journal:  Hum Genet       Date:  2021-06-26       Impact factor: 4.132

3.  Common methods in mitochondrial research (Review).

Authors:  Yiyuan Yin; Haitao Shen
Journal:  Int J Mol Med       Date:  2022-08-25       Impact factor: 5.314

4.  A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome.

Authors:  Yoshihito Kishita; Kaori Ishikawa; Kazuto Nakada; Jun-Ichi Hayashi; Takuya Fushimi; Masaru Shimura; Masakazu Kohda; Akira Ohtake; Kei Murayama; Yasushi Okazaki
Journal:  Sci Rep       Date:  2021-05-27       Impact factor: 4.379

  4 in total

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