Literature DB >> 11170211

Pex, analytical tools for PDB files. I. GF-Pex: basic file to describe a protein.

A Thomas1, O Bouffioux, D Geeurickx, R Brasseur.   

Abstract

Pex are created to extract numeric and string descriptions of protein structures from PDB files. This concerns covalent bond lengths and angles, secondary structures, residues in interaction, H-bond lengths and geometry, etc. Several kinds of Pex are generated: (1) general feature (GF-Pex); (2) H-bond (H-Pex); and (3) accessible surface (AS-Pex) and force potential (FP-Pex). We describe the general principles of Pex and detail the GF-Pex files. Using the GF-Pex of 131 proteins, we analyze the mean residue frequencies, the straight phi/psi distribution and the major kinds of secondary structures in proteins. Thomas et al. (this issue) analyzes the main chain H-bonds in those proteins. The GF-Pex and H-Pex files of the 131 proteins can be downloaded from the CBMN site (http://www.fsagx.ac.be/bp/). Proteins 2001;43:28-36. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11170211

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  5 in total

1.  "De novo" design of peptides with specific lipid-binding properties.

Authors:  L Lins; B Charloteaux; C Heinen; A Thomas; R Brasseur
Journal:  Biophys J       Date:  2005-11-04       Impact factor: 4.033

2.  Analysis of accessible surface of residues in proteins.

Authors:  Laurence Lins; Annick Thomas; Robert Brasseur
Journal:  Protein Sci       Date:  2003-07       Impact factor: 6.725

3.  A combination of compositional index and genetic algorithm for predicting transmembrane helical segments.

Authors:  Nazar Zaki; Salah Bouktif; Sanja Lazarova-Molnar
Journal:  PLoS One       Date:  2011-07-26       Impact factor: 3.240

4.  A new in-silico method for determination of helical transmembrane domains based on the PepLook scan: application to IL-2Rβ and IL-2Rγc receptor chains.

Authors:  Yan Charlois; Laurence Lins; Robert Brasseur
Journal:  BMC Struct Biol       Date:  2011-05-24

5.  Distantly related lipocalins share two conserved clusters of hydrophobic residues: use in homology modeling.

Authors:  Benoit Adam; Benoit Charloteaux; Jerome Beaufays; Luc Vanhamme; Edmond Godfroid; Robert Brasseur; Laurence Lins
Journal:  BMC Struct Biol       Date:  2008-01-11
  5 in total

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