Tryptophan Oxidation in the UQCRC1 Subunit of Mitochondrial Complex III (Ubiquinol-Cytochrome C Reductase) in a Mouse Model of Myodegeneration Causes Large Structural Changes in the Complex: A Molecular Dynamics Simulation Study-Reference-Cited by-同舟云学术

Tryptophan Oxidation in the UQCRC1 Subunit of Mitochondrial Complex III (Ubiquinol-Cytochrome C Reductase) in a Mouse Model of Myodegeneration Causes Large Structural Changes in the Complex: A Molecular Dynamics Simulation Study

Published:2019-07-23 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Unni Sruthi,Thiyagarajan S.^ORCID,Srinivas Bharath M. M.,Padmanabhan B.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-47018-6.pdf

Reference22 articles.

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2. Ramadasan-Nair, R. et al. Mitochondrial alterations and oxidative stress in an acute transient mouse model of muscle degeneration: implications for muscular dystrophy and related muscle pathologies. J. Biol Chem. 289, 485–509 (2014).

3. Sunitha, B. et al. Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function. J. Neurochem. 138, 174–191 (2016).

4. Debashree, B. et al. Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder. J. Neurochem. 145(4), 323–341 (2018).

5. Renjini, R., Gayathri, N., Nalini, A. & Srinivas Bharath, M. M. Oxidative damage in muscular dystrophy correlates with the severity of the pathology: role of glutathione metabolism. Neurochem Res. 37, 885–898 (2012).

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