Jove
Visualize
Contact Us

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.
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.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...

You might also read

Related Articles

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

Sort by
Same author

Fibril Structure of Desiccation-Protective Tardigrade Protein CAHS-8.

Angewandte Chemie (International ed. in English)·2025
Same author

Deciphering conformational dynamics in AFM data using fast nonlinear NMA and FFT-based search with AFMFit.

Communications biology·2025
Same author

Lipopolysaccharide nanoparticles: A biomimetic platform to study bacterial surface.

Biophysical journal·2025
Same author

Perspectives Toward an Integrative Structural Biology Pipeline With Atomic Force Microscopy Topographic Images.

Journal of molecular recognition : JMR·2024
Same author

PyFMLab: Open-source software for atomic force microscopy microrheology data analysis.

Open research Europe·2024
Same author

Cryo-EM structure of influenza helical nucleocapsid reveals NP-NP and NP-RNA interactions as a model for the genome encapsidation.

Science advances·2023
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 Video

Updated: May 7, 2026

Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis
08:49

Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis

Published on: June 20, 2025

DockAFM: benchmarking protein structures by docking under AFM topographs.

Rui C Chaves1, Jean-Luc Pellequer

  • 1CEA, iBEB, Service de Biochimie et Toxicologie Nucléaire, F-30207 Bagnols sur Cèze, France.

Bioinformatics (Oxford, England)
|October 1, 2013
PubMed
Summary
This summary is machine-generated.

We developed DockAFM, a server to compare 3D protein structures with atomic force microscopy data. This tool assesses protein structural variability and agreement with experimental topographical surfaces.

More Related Videos

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
05:08

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

Related Experiment Videos

Last Updated: May 7, 2026

Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis
08:49

Incorporating Target Protein Structure Flexibility and Dynamics in Computational Drug Discovery Using Ensemble-Based Docking Analysis

Published on: June 20, 2025

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
05:08

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

Area of Science:

  • Biophysics
  • Structural Biology
  • Computational Biology

Background:

  • Proteins exist in multiple conformations, influencing their function.
  • Experimental techniques like atomic force microscopy (AFM) provide topographical data of biomolecules.
  • Comparing theoretical 3D structures with experimental data is crucial for validation.

Purpose of the Study:

  • To present a computational server, DockAFM, for scoring the agreement between 3D atomic protein structures and experimental AFM envelopes.
  • To enable the assessment of protein structural variability using topographical data.

Main Methods:

  • Development of a server (DockAFM) that computes agreement scores.
  • Utilizing AFM-obtained experimental envelopes.
  • Testing with three distinct protein structures: immunoglobulins (IgG) and activated blood coagulation factor V.

Main Results:

  • Successfully computed the agreement between tested protein structures and topographical surfaces.
  • Demonstrated the server's capability to evaluate structural conformity with experimental data.

Conclusions:

  • The DockAFM server provides a straightforward method for comparing 3D protein structures with experimental AFM data.
  • This approach is valuable for investigating structural variability within protein families.