Literature DB >> 17238691

Applying sequential forward floating selection to protein structure prediction with a study of HIV-1 PR.

Jeff Reneker1, Chi-Ren Shyu.   

Abstract

Accurate structural models of target proteins are an essential component to structure-based drug design methods. To aid in this effort, the sequential forward floating selection (SFFS) algorithm is being applied to protein structure prediction. This algorithm demonstrates a reasonable balance between optimity of feature selection and efficiency while using large datasets such as the protein databank (PDB). The resulting protein structure predictions will be used in a study of HIV-1 PR.

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Year:  2006        PMID: 17238691      PMCID: PMC1839351     

Source DB:  PubMed          Journal:  AMIA Annu Symp Proc        ISSN: 1559-4076


  3 in total

Review 1.  Inhibitors of HIV-1 protease: a major success of structure-assisted drug design.

Authors:  A Wlodawer; J Vondrasek
Journal:  Annu Rev Biophys Biomol Struct       Date:  1998

2.  Structure-based inhibitor design by using protein models for the development of antiparasitic agents.

Authors:  C S Ring; E Sun; J H McKerrow; G K Lee; P J Rosenthal; I D Kuntz; F E Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

3.  Limited sequence diversity of the HIV type 1 protease gene from clinical isolates and in vitro susceptibility to HIV protease inhibitors.

Authors:  D L Winslow; S Stack; R King; H Scarnati; A Bincsik; M J Otto
Journal:  AIDS Res Hum Retroviruses       Date:  1995-01       Impact factor: 2.205

  3 in total

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