Literature DB >> 16383657

Improvement on a simplified model for protein folding simulation.

Ming Zhang1, Changjun Chen, Yi He, Yi Xiao.   

Abstract

Improvements were made on a simplified protein model--the Ramachandran model-to achieve better computer simulation of protein folding. To check the validity of such improvements, we chose the ultrafast folding protein Engrailed Homeodomain as an example and explored several aspects of its folding. The engrailed homeodomain is a mainly alpha-helical protein of 61 residues from Drosophila melanogaster. We found that the simplified model of Engrailed Homeodomain can fold into a global minimum state with a tertiary structure in good agreement with its native structure.

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Year:  2005        PMID: 16383657     DOI: 10.1103/PhysRevE.72.051919

Source DB:  PubMed          Journal:  Phys Rev E Stat Nonlin Soft Matter Phys        ISSN: 1539-3755


  2 in total

1.  Refolding the engrailed homeodomain: structural basis for the accumulation of a folding intermediate.

Authors:  Michelle E McCully; David A C Beck; Alan R Fersht; Valerie Daggett
Journal:  Biophys J       Date:  2010-09-08       Impact factor: 4.033

2.  Stability and folding behavior analysis of zinc-finger using simple models.

Authors:  Shan Chang; Xiong Jiao; Jian-Ping Hu; Yan Chen; Xu-Hong Tian
Journal:  Int J Mol Sci       Date:  2010-10-19       Impact factor: 5.923

  2 in total

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