NIAS-Server

NIAS-Server analyzes conformational preferences of amino acid residues and secondary structures in experimentally determined three-dimensional protein structures and computes probability densities for use in structure validation, prediction, fold and motif characterization, and protein design.


Key Features:

  • Conformational Preference Analysis: Extracts detailed conformational preferences of amino acid residues and secondary structures from experimentally determined three-dimensional protein structures.
  • Structure Validation and Prediction: Computes probability densities of amino acid conformations for assessing and comparing predicted and experimental protein models.
  • Characterization of Protein Folds and Motifs: Provides conformational data used to characterize protein folds and local structural motifs.
  • Applications in Protein Structure Prediction and Design: Supplies residue-specific conformational tendencies that inform protein structure prediction and rational protein design.

Scientific Applications:

  • Protein Structure Analysis: Analyzing detailed residue conformations within solved protein structures.
  • Molecular Folding Studies: Investigating how proteins fold into their functional three-dimensional shapes using residue conformational preferences.
  • Structure-Based Drug Design: Using conformational preference data to inform design of drugs that interact with specific protein structural features.

Methodology:

Analyzes a repository of experimentally determined protein structures to extract conformational preferences of amino acids and computes probability density distributions from the extracted data.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Borguesan B, Inostroza-Ponta M, Dorn M. NIAS-Server: Neighbors Influence of Amino acids and Secondary Structures in Proteins. Journal of Computational Biology. 2017;24(3):255-265. doi:10.1089/cmb.2016.0074. PMID:27494258.

Documentation

Links