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Molecular Mechanisms of Disease-Causing Missense Mutations

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 425, Issue 21, Pages 3919-3936

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2013.07.014

Keywords

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Funding

  1. National Institutes of Health [R01GM093937]
  2. Intramural Research Program of the National Library of Medicine at the US National Institutes of Health
  3. Grants-in-Aid for Scientific Research [13J03101] Funding Source: KAKEN

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Genetic variations resulting in a change of amino acid sequence can have a dramatic effect on stability, hydrogen bond network, conformational dynamics, activity and many other physiologically important properties of proteins. The substitutions of only one residue in a protein sequence, so-called missense mutations, can be related to many pathological conditions and may influence susceptibility to disease and drug treatment. The plausible effects of nnissense mutations range from affecting the macromolecular stability to perturbing macronnolecular interactions and cellular localization. Here we review the individual cases and genome-wide studies that illustrate the association between missense mutations and diseases. In addition, we emphasize that the molecular mechanisms of effects of mutations should be revealed in order to understand the disease origin. Finally, we report the current state-of-the-art methodologies that predict the effects of mutations on protein stability, the hydrogen bond network, pH dependence, conformational dynamics and protein function. Published by Elsevier Ltd.

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