Literature DB >> 20129805

Sphericity of a protein via the beta-complex.

Deok-Soo Kim1, Jae-Kwan Kim, Chung-In Won, Chong-Min Kim, Joon Young Park, Jong Bhak.   

Abstract

Molecular shape is a fundamental factor in determining the function of a molecule. As proteins tend to fold into globular shapes, the shape descriptor for protein sphericity is important in understanding molecular functions. In this paper, a definition of protein sphericity is introduced based on the recently developed geometric constructs of the beta-complex and beta-shape of a protein. The beta-complex represents the Euclidean proximity among all the atoms in a protein, and the beta-shape is the polyhedron contained within the boundary of the corresponding beta-complex. Hence, the beta-shape determines the proximity among the atoms on the boundary of a protein. Given the volume of a beta-shape, the ratio between the surface area of a sphere with this volume and the surface area of the beta-shape itself is a good measure to classify the sphericity of a protein, especially when the radius of a probe is 3.0 A. The presented measure is invariant to translation and rotation. (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20129805     DOI: 10.1016/j.jmgm.2010.01.001

Source DB:  PubMed          Journal:  J Mol Graph Model        ISSN: 1093-3263            Impact factor:   2.518


  1 in total

1.  Use of circular variance to quantify the deviation of a macromolecule from the spherical shape.

Authors:  Mihaly Mezei
Journal:  J Math Chem       Date:  2015-08-20       Impact factor: 2.357

  1 in total

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