Literature DB >> 18186486

Hydrophobic clusters in protein structures.

J Arunachalam1, N Gautham.   

Abstract

Globular proteins fold such that the hydrophobic groups are packed inside forming hydrophobic clusters, and the hydrophilic groups are present on the surface. In this article we analyze clusters of hydrophobic groups of atoms in 781 protein structures selected from the PDB. Our analysis showed that every structure consists of two types of clusters: at least one large cluster that forms the hydrophobic core and probably dictates the protein fold; and numerous smaller clusters, which might be involved in the stabilization of the fold. We also analyzed the preference of the hydrophobic groups in each of the amino acids toward forming hydrophobic clusters. We find that hydrophobic groups from the hydrophilic amino acids also contribute toward cluster formation. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18186486     DOI: 10.1002/prot.21881

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


  2 in total

1.  Ca2+ and Mg2+ modulate conformational dynamics and stability of downstream regulatory element antagonist modulator.

Authors:  Khoa Pham; Gangadhar Dhulipala; Walter G Gonzalez; Bernard S Gerstman; Chola Regmi; Prem P Chapagain; Jaroslava Miksovska
Journal:  Protein Sci       Date:  2015-03-10       Impact factor: 6.725

2.  The origin of β-strand bending in globular proteins.

Authors:  Kazuo Fujiwara; Shinichi Ebisawa; Yuka Watanabe; Hiromi Fujiwara; Masamichi Ikeguchi
Journal:  BMC Struct Biol       Date:  2015-10-22
  2 in total

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