Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Sequence walkers: a graphical method to display how binding proteins interact with DNA or RNA sequences

T D Schneider1

  • 1National Cancer Institute, Frederick Cancer Research and Development Center, Laboratory of Mathematical Biology, Frederick, MD 21702-1201, USA.

Nucleic Acids Research
|October 23, 1997
PubMed
Summary

This study introduces a graphical method using sequence "walkers" to visualize macromolecule interactions with nucleotide sequences, aiding in binding site identification and engineering.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Strong minor groove base conservation in sequence logos implies DNA distortion or base flipping during replication and transcription initiation.

Nucleic acids research·2001
Same author

The P1 phage replication protein RepA contacts an otherwise inaccessible thymine N3 proton by DNA distortion or base flipping.

Nucleic acids research·2001
Same author

Anatomy of Escherichia coli ribosome binding sites.

Journal of molecular biology·2001
Same author

Computation-directed identification of OxyR DNA binding sites in Escherichia coli.

Journal of bacteriology·2001
Same author

The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.

Nucleic acids research·2001
Same author

Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A>G; IVS11-2A>G; L78833, 37698, A>G.

Human mutation·2000

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Molecular Biology

Background:

  • Understanding protein-nucleic acid interactions is crucial for deciphering gene regulation.
  • Current methods for analyzing these interactions can be complex and lack intuitive visualization.

Purpose of the Study:

  • To present a novel graphical method for visualizing macromolecule binding to nucleotide sequences.
  • To enable quantitative analysis and engineering of binding sites.
  • To facilitate the identification of database anomalies and prediction of sequence variations.

Main Methods:

  • Development of sequence 'walkers' that graphically represent favorable/unfavorable base contacts.
  • Utilizing letter orientation and height to denote contact type and contribution to sequence conservation.

Related Experiment Videos

  • Stepping walkers along sequence data for visual searching and mapping.
  • Sequence alteration for engineering binding sites and predicting variations.
  • Main Results:

    • The graphical method provides an intuitive display of binding interactions.
    • Sequence walkers allow for visual searching and quantitative mapping of binding sites.
    • The method enables quantitative engineering of binding sites.
    • Visualization of database anomalies and prediction of polymorphisms versus mutations is possible.

    Conclusions:

    • The sequence walker method offers a powerful and versatile tool for analyzing and manipulating DNA-protein interactions.
    • This approach enhances the understanding of molecular recognition and facilitates applications in genetic engineering and data analysis.