Literature DB >> 20223222

Deciphering the deformation modes associated with function retention and specialization in members of the Ras superfamily.

Francesco Raimondi1, Modesto Orozco, Francesca Fanelli.   

Abstract

The evolutionary and physical deformability patterns of members of the Ras GTPase superfamily were investigated by Principal Component and Elastic Network-Normal Mode analyses. The study helped to decipher the dynamics information encrypted into the conserved core and to separate the trans-family intrinsic flexibility associated with a common function from the protein motions related to functional specialization of selected families or family members. The conserved core is dynamically divided into two lobes. The deformation modes, which allow the Ras GTPases to accomplish their switching function, are conserved along evolution and are localized in lobe 1 portions close to the nucleotide. These modes lead to functional specialization when associated with evolution-driven deformations of protein portions essentially located in lobe 2, distal from the nucleotide, and involved in peculiar interactions with membrane, guanine nucleotide exchange factors, or effectors. Overall, a complete picture of the functional and evolutionary dynamics of the Ras superfamily emerges.

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Year:  2010        PMID: 20223222     DOI: 10.1016/j.str.2009.12.015

Source DB:  PubMed          Journal:  Structure        ISSN: 0969-2126            Impact factor:   5.006


  20 in total

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Review 2.  Lessons from computer simulations of Ras proteins in solution and in membrane.

Authors:  Priyanka Prakash; Alemayehu A Gorfe
Journal:  Biochim Biophys Acta       Date:  2013-07-30

3.  Oncogenic K-Ras Binds to an Anionic Membrane in Two Distinct Orientations: A Molecular Dynamics Analysis.

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Review 4.  Adaptability of protein structures to enable functional interactions and evolutionary implications.

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Journal:  Curr Opin Struct Biol       Date:  2015-08-06       Impact factor: 6.809

Review 5.  Membrane orientation dynamics of lipid-modified small GTPases.

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7.  Nucleotide binding switches the information flow in ras GTPases.

Authors:  Francesco Raimondi; Guillem Portella; Modesto Orozco; Francesca Fanelli
Journal:  PLoS Comput Biol       Date:  2011-03-03       Impact factor: 4.475

8.  Conformational and functional analysis of molecular dynamics trajectories by self-organising maps.

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9.  ProDy: protein dynamics inferred from theory and experiments.

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10.  Molecular dynamics of mesophilic-like mutants of a cold-adapted enzyme: insights into distal effects induced by the mutations.

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