Literature DB >> 33164889

Functional effects of protein variants.

Mauno Vihinen1.   

Abstract

Genetic and other variations frequently affect protein functions. Scientific articles can contain confusing descriptions about which function or property is affected, and in many cases the statements are pure speculation without any experimental evidence. To clarify functional effects of protein variations of genetic or non-genetic origin, a systematic conceptualisation and framework are introduced. This framework describes protein functional effects on abundance, activity, specificity and affinity, along with countermeasures, which allow cells, tissues and organisms to tolerate, avoid, repair, attenuate or resist (TARAR) the effects. Effects on abundance discussed include gene dosage, restricted expression, mis-localisation and degradation. Enzymopathies, effects on kinetics, allostery and regulation of protein activity are subtopics for the effects of variants on activity. Variation outcomes on specificity and affinity comprise promiscuity, specificity, affinity and moonlighting. TARAR mechanisms redress variations with active and passive processes including chaperones, redundancy, robustness, canalisation and metabolic and signalling rewiring. A framework for pragmatic protein function analysis and presentation is introduced. All of the mechanisms and effects are described along with representative examples, most often in relation to diseases. In addition, protein function is discussed from evolutionary point of view. Application of the presented framework facilitates unambiguous, detailed and specific description of functional effects and their systematic study.
Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.

Keywords:  Abundance; Activity; Affinity; Bioinformatics; Mutation; Protein function; Protein functional effect; Protein variation; Specificity

Mesh:

Substances:

Year:  2020        PMID: 33164889     DOI: 10.1016/j.biochi.2020.10.009

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  7 in total

1.  Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants.

Authors:  Souhrid Mukherjee; Thomas A Cassini; Ningning Hu; Tao Yang; Bian Li; Wangzhen Shen; Christopher W Moth; David C Rinker; Jonathan H Sheehan; Joy D Cogan; John H Newman; Rizwan Hamid; Robert L Macdonald; Dan M Roden; Jens Meiler; Georg Kuenze; John A Phillips; John A Capra
Journal:  HGG Adv       Date:  2022-07-19

2.  When a Synonymous Variant Is Nonsynonymous.

Authors:  Mauno Vihinen
Journal:  Genes (Basel)       Date:  2022-08-19       Impact factor: 4.141

Review 3.  Individual Genetic Heterogeneity.

Authors:  Mauno Vihinen
Journal:  Genes (Basel)       Date:  2022-09-10       Impact factor: 4.141

4.  Molecular Dynamic Simulation Reveals Structure Differences in APOL1 Variants and Implication in Pathogenesis of Chronic Kidney Disease.

Authors:  Richard Mayanja; Christopher Kintu; Oudou Diabate; Opeyemi Soremekun; Olugbenga Oluseun Oluwagbemi; Mamadou Wele; Robert Kalyesubula; Daudi Jjingo; Tinashe Chikowore; Segun Fatumo
Journal:  Genes (Basel)       Date:  2022-08-16       Impact factor: 4.141

5.  Generic model for biological regulation.

Authors:  Mauno Vihinen
Journal:  F1000Res       Date:  2022-04-13

Review 6.  Computational approaches for predicting variant impact: An overview from resources, principles to applications.

Authors:  Ye Liu; William S B Yeung; Philip C N Chiu; Dandan Cao
Journal:  Front Genet       Date:  2022-09-29       Impact factor: 4.772

7.  Pathogenic variation types in human genes relate to diseases through Pfam and InterPro mapping.

Authors:  Giulia Babbi; Castrense Savojardo; Davide Baldazzi; Pier Luigi Martelli; Rita Casadio
Journal:  Front Mol Biosci       Date:  2022-09-16
  7 in total

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