Literature DB >> 22809383

P.R.E.S.S.--an R-package for exploring residual-level protein structural statistics.

Yuanyuan Huang1, Stephen Bonett, Andrzej Kloczkowski, Robert Jernigan, Zhijun Wu.   

Abstract

P.R.E.S.S. is an R-package developed to allow researchers to get access to and manipulate a large set of statistical data on protein residue-level structural properties such as residue-level virtual bond lengths, virtual bond angles, and virtual torsion angles. A large set of high-resolution protein structures is downloaded and surveyed. Their residue-level structural properties are calculated and documented. The statistical distributions and correlations of these properties can be queried and displayed. Tools are also provided for modeling and analyzing a given structure in terms of its residue-level structural properties. In particular, new tools for computing residue-level statistical potentials and displaying residue-level Ramachandran-like plots are developed for structural analysis and refinement. P.R.E.S.S. has been released in R as an open source software package, with a user-friendly GUI, accessible and executable by a public user in any R environment. P.R.E.S.S. can also be downloaded directly at http://www.math.iastate.edu/press/.

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Year:  2012        PMID: 22809383      PMCID: PMC4373622          DOI: 10.1142/S0219720012420073

Source DB:  PubMed          Journal:  J Bioinform Comput Biol        ISSN: 0219-7200            Impact factor:   1.122


  17 in total

1.  Protein structure determination using a database of interatomic distance probabilities.

Authors:  M E Wall; S Subramaniam; G N Phillips
Journal:  Protein Sci       Date:  1999-12       Impact factor: 6.725

Review 2.  Rotamer libraries in the 21st century.

Authors:  Roland L Dunbrack
Journal:  Curr Opin Struct Biol       Date:  2002-08       Impact factor: 6.809

3.  BioMagResBank database with sets of experimental NMR constraints corresponding to the structures of over 1400 biomolecules deposited in the Protein Data Bank.

Authors:  Jurgen F Doreleijers; Steve Mading; Dimitri Maziuk; Kassandra Sojourner; Lei Yin; Jun Zhu; John L Markley; Eldon L Ulrich
Journal:  J Biomol NMR       Date:  2003-06       Impact factor: 2.835

4.  Refinement of NMR-determined protein structures with database derived distance constraints.

Authors:  Feng Cui; Robert Jernigan; Zhijun Wu
Journal:  J Bioinform Comput Biol       Date:  2005-12       Impact factor: 1.122

5.  Bio3d: an R package for the comparative analysis of protein structures.

Authors:  Barry J Grant; Ana P C Rodrigues; Karim M ElSawy; J Andrew McCammon; Leo S D Caves
Journal:  Bioinformatics       Date:  2006-08-29       Impact factor: 6.937

Review 6.  Protein-folding dynamics: overview of molecular simulation techniques.

Authors:  Harold A Scheraga; Mey Khalili; Adam Liwo
Journal:  Annu Rev Phys Chem       Date:  2007       Impact factor: 12.703

7.  Refinement of NMR-determined protein structures with database derived mean-force potentials.

Authors:  Di Wu; Robert Jernigan; Zhijun Wu
Journal:  Proteins       Date:  2007-07-01

8.  PRTAD: a database for protein residue torsion angle distributions.

Authors:  Xiaoyong Sun; Wu Di; Robert Jernigan; Zhijun Wu
Journal:  Int J Data Min Bioinform       Date:  2009       Impact factor: 0.667

9.  Refinement of under-determined loops of Human Prion Protein by database-derived distance constraints.

Authors:  Feng Cui; Kriti Mukhopadhyay; Won-Bin Young; Robert L Jernigan; Zhijun Wu
Journal:  Int J Data Min Bioinform       Date:  2009       Impact factor: 0.667

10.  PIDD: database for Protein Inter-atomic Distance Distributions.

Authors:  Di Wu; Feng Cui; Robert Jernigan; Zhijun Wu
Journal:  Nucleic Acids Res       Date:  2006-12-06       Impact factor: 16.971

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  1 in total

1.  Protein Structure Classification and Loop Modeling Using Multiple Ramachandran Distributions.

Authors:  Seyed Morteza Najibi; Mehdi Maadooliat; Lan Zhou; Jianhua Z Huang; Xin Gao
Journal:  Comput Struct Biotechnol J       Date:  2017-02-08       Impact factor: 7.271

  1 in total

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