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Related Concept Videos

Protein and Protein Structure02:15

Protein and Protein Structure

Proteins are one of the most abundant organic molecules in living systems and have the most diverse range of functions of all macromolecules. Proteins may be structural, regulatory, contractile, or protective. They may serve in transport, storage, or membranes; or they may be toxins or enzymes. Their structures, like their functions, vary greatly. They are all, however, amino acid polymers arranged in a linear sequence.
A protein's shape is critical to its function. For example, an enzyme can...
Protein Folding01:22

Protein Folding

Overview
Protein Folding01:25

Protein Folding

Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
Protein Folding01:22

Protein Folding

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Protein and Protein Structures02:15

Protein and Protein Structures

Proteins are one of the most abundant organic molecules in living systems and have the most diverse range of functions of all macromolecules. Proteins may be structural, regulatory, contractile, or protective. They may serve in transport, storage, or membranes; or they may be toxins or enzymes. Their structures, like their functions, vary greatly. They are all, however, amino acid polymers arranged in a linear sequence.
A protein's shape is critical to its function. For example, an enzyme can...
Protein Organization01:24

Protein Organization

Proteins are polymers of amino acid residues. They are versatile and responsible for different cellular functions, including DNA replication, molecular transport, catalysis, and structural support. Proteins have a hierarchical structure comprising at least three levels of organization: primary, secondary, and tertiary structure. Some large proteins have a quaternary structure where individual protein subunits are linked together.
The primary structure of a protein is its amino acid sequence.

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Updated: Jun 4, 2026

A Protocol for Computer-Based Protein Structure and Function Prediction
16:41

A Protocol for Computer-Based Protein Structure and Function Prediction

Published on: November 3, 2011

FPGA accelerator for protein secondary structure prediction based on the GOR algorithm.

Fei Xia1, Yong Dou, Guoqing Lei

  • 1National Laboratory for Parallel&Distributed Processing, Department of Computer Science, National University of Defense Technology, ChangSha, 410073, China.

BMC Bioinformatics
|February 24, 2011
PubMed
Summary
This summary is machine-generated.

This study accelerates protein structure prediction using FPGA hardware for the GOR-IV algorithm, achieving over 430x speedup. The novel implementation significantly enhances computational efficiency while reducing power consumption compared to traditional CPUs.

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Last Updated: Jun 4, 2026

A Protocol for Computer-Based Protein Structure and Function Prediction
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Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
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10:58

Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules

Published on: July 25, 2013

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Biophysics

Background:

  • Protein structure dictates function, making prediction crucial.
  • The GOR algorithm is a key tool for protein secondary structure prediction.
  • Increasing protein data necessitates faster prediction methods.

Purpose of the Study:

  • To accelerate the GOR-IV algorithm for 2D protein structure prediction.
  • To develop a fine-grained parallel hardware implementation on FPGA.
  • To address the computational demands of large protein databases.

Main Methods:

  • Implemented a parallel hardware architecture on an FPGA (XC5VLX330).
  • Partitioned parameter tables for parallel access and exploited data reuse.
  • Pipelined computation to overlap sequence loading, computing, and back-writing.

Main Results:

  • Achieved a speedup of over 430x compared to the original GOR-IV.
  • Demonstrated a 110x speedup versus a multi-thread SIMD PC implementation.
  • Reduced power consumption to approximately 30% of general-purpose CPUs.

Conclusions:

  • FPGA acceleration offers significant performance gains for GOR-IV.
  • The proposed method provides a highly efficient and power-saving solution for protein structure prediction.
  • This approach is well-suited for accelerating bioinformatics algorithms.