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Related Concept Videos

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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Conserved Binding Sites01:49

Conserved Binding Sites

Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
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Evolutionary Relationships through Genome Comparisons

Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Nucleic Acid Structure

The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
DNA Structure
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Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.

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Analyzing and Building Nucleic Acid Structures with 3DNA
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Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

DNA reference alignment benchmarks based on tertiary structure of encoded proteins.

Hyrum Carroll1, Wesley Beckstead, Timothy O'Connor

  • 1Computer Science Department, Brigham Young University, Provo, Utah 84602, USA. hyrumdc@gmail.com

Bioinformatics (Oxford, England)
|August 10, 2007
PubMed
Summary

Researchers have developed the first multiple DNA sequence alignment benchmarks, crucial for evaluating bioinformatics tools. These new DNA sequence alignment databases enable accurate assessment of multiple sequence alignment (MSA) programs for DNA.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Multiple sequence alignments (MSAs) are fundamental in bioinformatics.
  • Existing benchmarks primarily focus on protein sequences, leaving a gap for DNA sequence analysis.
  • Accurate evaluation of multiple DNA sequence alignment (MDSA) programs is hindered by the lack of standardized DNA benchmarks.

Purpose of the Study:

  • To introduce the first comprehensive benchmarks for multiple DNA sequence alignment.
  • To provide a resource for quantitatively evaluating the performance of MDSA applications.
  • To facilitate the development and validation of novel algorithms for DNA sequence alignment.

Main Methods:

  • Construction of DNA benchmarks using protein-coding DNA regions.
  • Incorporation of biological features, including tertiary structures of encoded proteins, into benchmark design.
  • Development of two database versions (mdsa_100s and mdsa_all) with varying sequence identity thresholds.

Main Results:

  • Creation of reference DNA databases comprising 3545 alignments and 68,581 sequences.
  • The databases are structured to enable rigorous benchmarking of MDSA tools.
  • A case study demonstrating the utility of the benchmarks for evaluating MSA performance is provided.

Conclusions:

  • The developed benchmarks address a critical need for evaluating DNA sequence alignment tools.
  • These resources will significantly advance the field of bioinformatics by enabling standardized performance assessment.
  • The availability of these benchmarks is expected to spur innovation in multiple DNA sequence alignment methodologies.