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 Concept Videos

Ligand Binding and Linkage00:49

Ligand Binding and Linkage

6.0K
Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence...
6.0K
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

4.3K
4.3K
Conserved Binding Sites01:49

Conserved Binding Sites

5.3K
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...
5.3K
Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

9.4K
Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
9.4K
Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

2.8K
2.8K
Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

3.2K
3.2K

You might also read

Related Articles

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

Sort by
Same author

Simple and Thorough Detection of Related Sequences with Position-Varying Probabilities of Substitutions, Insertions, and Deletions.

Journal of computational biology : a journal of computational molecular cell biology·2026
Same author

Probability-Based Sequence Comparison Finds Pre-Eutherian Nuclear Mitochondrial DNA Segments in Mammalian Genomes.

Journal of computational biology : a journal of computational molecular cell biology·2026
Same author

Further varieties of ancient endogenous retrovirus in human DNA.

Mobile DNA·2025
Same author

Hybrid analysis with phylogeny and population modeling to estimate the recent founding date of a population: A case study in the origins of COVID-19 illustrates how a branching process approximation can simplify a hybrid analysis.

Mathematical biosciences·2025
Same author

Increasing Representativeness in the <i>All of Us</i> Cohort Using Inverse Probability Weighting.

medRxiv : the preprint server for health sciences·2025
Same author

The Statistics of Parametrized Syncmers in a Simple Mutation Process Without Spurious Matches.

Journal of computational biology : a journal of computational molecular cell biology·2024
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)·2026
Same journal

EDEL: Enhancing Dense Retrievers for Curation of Biomedical Knowledge Bases.

Bioinformatics (Oxford, England)·2026
Same journal

Informative Relational Learning for Adverse Reaction Prediction with Enhanced Generalization to Novel Drugs.

Bioinformatics (Oxford, England)·2026
Same journal

An interpretable deep learning framework uncovers features governing CRISPR-Cas9 genome-editing efficiency.

Bioinformatics (Oxford, England)·2026
Same journal

3DICE: Interpretable 3D Cross-Modal Learning for Drug-Target Interaction Prediction and Large-Scale Drug Discovery.

Bioinformatics (Oxford, England)·2026
See all related articles

Related Experiment Video

Updated: Apr 1, 2026

A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

36.3K

ALP & FALP: C++ libraries for pairwise local alignment E-values.

Sergey Sheetlin1, Yonil Park1, Martin C Frith2

  • 1National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, MD 20894, USA and.

Bioinformatics (Oxford, England)
|October 3, 2015
PubMed
Summary
This summary is machine-generated.

The Ascending Ladder Program (ALP) and Frameshift Ascending Ladder Program (FALP) provide rapid E-value calculations for DNA and protein sequence alignments. Source code is publicly available for integration into C++ bioinformatics programs.

More Related Videos

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

70.1K
Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine
10:40

Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine

Published on: December 22, 2017

11.1K

Related Experiment Videos

Last Updated: Apr 1, 2026

A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

36.3K
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

70.1K
Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine
10:40

Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine

Published on: December 22, 2017

11.1K

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Molecular Biology

Background:

  • Pairwise local alignment is a critical tool for molecular biologists.
  • Accurate E-value calculation is essential for sequence alignment interpretation.
  • Existing methods may lack speed or flexibility for diverse alignment types.

Purpose of the Study:

  • To introduce efficient algorithms for calculating E-values in sequence alignment.
  • To provide tools for both standard local alignments and frameshifted alignments.
  • To enable widespread adoption and integration of these computational methods.

Main Methods:

  • Development of the Ascending Ladder Program (ALP) for rapid E-value calculation.
  • Development of the Frameshift Ascending Ladder Program (FALP) for frameshifted alignments.
  • Implementation of algorithms to handle arbitrary substitution matrices, gap costs, and letter abundances.

Main Results:

  • ALP achieves real-time E-value calculations (approx. 1 second) for protein-protein and DNA-DNA local alignments.
  • FALP offers similar E-value calculations for frameshifted DNA-protein alignments, albeit with slightly longer computation times.
  • C++ source codes for both ALP and FALP are publicly available.

Conclusions:

  • ALP and FALP offer significant computational efficiencies for sequence alignment E-value determination.
  • The availability of source code facilitates the direct implementation of these algorithms by C++ programmers.
  • These tools enhance the capabilities of molecular biologists and bioinformaticians.