Literature DB >> 3818558

Radial locations of amino acid residues in a globular protein: correlation with the sequence.

K Nishikawa, T Ooi.   

Abstract

The location measure of a residue in a globular protein is defined as the number of C alpha atoms surrounding the residue located within a sphere of the radius of 14 A. This quantity is a measure of the exposure of a residue to solvent, and is related closely to the distance from the center of mass of a protein. In this work, the experimental value for each residue of a protein is obtained from the X-ray crystallographic data, and the quantity is also calculated from the amino acid sequence data by applying an empirical parameter set to it. The correlation between the experimental and computed quantities is as high as 0.50 on the average over 92 proteins of known three-dimensional structure. Therefore, the location measure of every residue in a globular protein is predictable with good accuracy from the sequence.

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Year:  1986        PMID: 3818558     DOI: 10.1093/oxfordjournals.jbchem.a121783

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  24 in total

1.  Improving prediction of helix-helix packing in membrane proteins using predicted contact numbers as restraints.

Authors:  Bian Li; Jeffrey Mendenhall; Elizabeth Dong Nguyen; Brian E Weiner; Axel W Fischer; Jens Meiler
Journal:  Proteins       Date:  2017-04-01

2.  Distance-constraint approach to higher-order structures of globular proteins with empirically determined distances between amino acid residues.

Authors:  H Wako; Y Kubota
Journal:  J Protein Chem       Date:  1991-04

3.  TOP-IDP-scale: a new amino acid scale measuring propensity for intrinsic disorder.

Authors:  Andrew Campen; Ryan M Williams; Celeste J Brown; Jingwei Meng; Vladimir N Uversky; A Keith Dunker
Journal:  Protein Pept Lett       Date:  2008       Impact factor: 1.890

4.  Improved genetic algorithm for the protein folding problem by use of a Cartesian combination operator.

Authors:  A A Rabow; H A Scheraga
Journal:  Protein Sci       Date:  1996-09       Impact factor: 6.725

5.  Segmentation of a protein into structural elements: analysis and classification of segments.

Authors:  H Nakashima; K Nishikawa; T Ooi
Journal:  J Protein Chem       Date:  1988-08

6.  De novo protein design using pairwise potentials and a genetic algorithm.

Authors:  D T Jones
Journal:  Protein Sci       Date:  1994-04       Impact factor: 6.725

7.  Structural determinants of limited proteolysis.

Authors:  Marat D Kazanov; Yoshinobu Igarashi; Alexey M Eroshkin; Piotr Cieplak; Boris Ratnikov; Ying Zhang; Zhanwen Li; Adam Godzik; Andrei L Osterman; Jeffrey W Smith
Journal:  J Proteome Res       Date:  2011-07-08       Impact factor: 4.466

8.  Molecular cloning of a cDNA of a camptothecin-resistant human DNA topoisomerase I and identification of mutation sites.

Authors:  H Tamura; C Kohchi; R Yamada; T Ikeda; O Koiwai; E Patterson; J D Keene; K Okada; E Kjeldsen; K Nishikawa
Journal:  Nucleic Acids Res       Date:  1991-01-11       Impact factor: 16.971

9.  Optimization of linear disorder predictors yields tight association between crystallographic disorder and hydrophobicity.

Authors:  Nathan B Holladay; Lisa N Kinch; Nick V Grishin
Journal:  Protein Sci       Date:  2007-10       Impact factor: 6.725

10.  Modelling a 3D structure for EgDf1 from Echinococcus granulosus: putative epitopes, phosphorylation motifs and ligand.

Authors:  M Paulino; A Esteves; M Vega; G Tabares; R Ehrlich; O Tapia
Journal:  J Comput Aided Mol Des       Date:  1998-07       Impact factor: 3.686

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