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Updated: May 22, 2026

Investigating Protein Sequence-structure-dynamics Relationships with Bio3D-web
Published on: July 16, 2017
Mining the protein data bank to differentiate error from structural variation in clustered static structures: an
Balasubramanian Venkatakrishnan1, Miorel-Lucian Palii, Mavis Agbandje-McKenna
1Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL 32610, USA. balavenkat@ufl.edu
Abstract:
The Protein Data Bank (PDB) contains over 71,000 structures. Extensively studied proteins have hundreds of submissions available, including mutations, different complexes, and space groups, allowing for application of data-mining algorithms to analyze an array of static structures and gain insight about a protein's structural variation and possibly its dynamics. This investigation is a case study of HIV protease (PR) using in-house algorithms for data mining and structure superposition through generalized formulæ that account for multiple conformations and fractional occupancies. Temperature factors (B-factors) are compared with spatial displacement from the mean structure over the entire study set and separately over bound and ligand-free structures, to assess the significance of structural deviation in a statistical context. Space group differences are also examined.
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