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

4.9K
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...
4.9K

You might also read

Related Articles

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

Sort by
Same author

Mutasynthesis and Antibiotic Activity of Mupirocin Analogues.

Chembiochem : a European journal of chemical biology·2026
Same author

Characterization of GUA-1, a chromosomally encoded ESBL from <i>Pseudomonas guariconensis-like</i>.

Antimicrobial agents and chemotherapy·2026
Same author

<i>In vitro</i> activity of aztreonam-avibactam and comparators against <i>Enterobacterales</i> isolated from bloodstream infections: ATLAS/ surveillance, 2021-2022.

Microbiology spectrum·2026
Same author

The Novel Carbapenem, JDB/PQ-1-219, Has Potent Broad Spectrum Activity against Multi-Drug Resistant <i>Acinetobacter baumannii</i>.

ACS infectious diseases·2026
Same author

Enhancing clinical utility of AI-based antimicrobial resistance models: a perspective.

mBio·2026
Same author

Linezolid Acts as a Selective Inhibitor of the JAK2 <sup>V617F</sup> Mutation.

bioRxiv : the preprint server for biology·2026
Same journal

Isavuconazole for invasive mold disease in patients with hematological malignancies: a multicenter real-world study from China on efficacy, safety, and competing risks.

Antimicrobial agents and chemotherapy·2026
Same journal

An Achilles' heel for methicillin-resistant <i>Staphylococcus aureus</i>? Re-evaluating β-lactam susceptibility of MRSA.

Antimicrobial agents and chemotherapy·2026
Same journal

Essential role of glycogen synthase kinase 3 in regulating growth, drug response, and infectivity in <i>Leishmania infantum</i>.

Antimicrobial agents and chemotherapy·2026
Same journal

<i>In vitro</i> antibacterial activity of gepotidacin in combination with other antimicrobial agents against <i>Neisseria gonorrhoeae</i> isolates.

Antimicrobial agents and chemotherapy·2026
Same journal

Development of domain-specific probes of <i>Plasmodium falciparum</i> heat shock protein 70-1.

Antimicrobial agents and chemotherapy·2026
Same journal

Addressing therapeutic options for KPC-3-producing ST307-<i>Klebsiella pneumoniae</i>: insights from <i>in vitro</i> evolution and mutant prevention strategies.

Antimicrobial agents and chemotherapy·2026
See all related articles

Related Experiment Video

Updated: Sep 20, 2025

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing
11:36

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing

Published on: July 3, 2016

11.0K

SAND: a comprehensive annotation of class D β-lactamases using structural alignment-based numbering.

Fedaa Attana1, Soobin Kim1, James Spencer2

  • 1UCL School of Pharmacy, University College London, London, United Kingdom.

Antimicrobial Agents and Chemotherapy
|May 27, 2025
PubMed
Summary
This summary is machine-generated.

Class D β-lactamases cause antibiotic resistance. A new standardized naming system (SAND) unifies residue and secondary structure annotations for class D β-lactamases, improving data comparison and accelerating research.

Keywords:
OXASANDclass Dsecondary structure annotationstructure-based sequence alignmentβ-lactamases

More Related Videos

The Use of a &#946;-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
08:06

The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions

Published on: February 1, 2018

9.1K
Creating and Applying a Reference to Facilitate the Discussion and Classification of Proteins in a Diverse Group
07:49

Creating and Applying a Reference to Facilitate the Discussion and Classification of Proteins in a Diverse Group

Published on: August 16, 2017

7.2K

Related Experiment Videos

Last Updated: Sep 20, 2025

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing
11:36

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing

Published on: July 3, 2016

11.0K
The Use of a &#946;-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
08:06

The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions

Published on: February 1, 2018

9.1K
Creating and Applying a Reference to Facilitate the Discussion and Classification of Proteins in a Diverse Group
07:49

Creating and Applying a Reference to Facilitate the Discussion and Classification of Proteins in a Diverse Group

Published on: August 16, 2017

7.2K

Area of Science:

  • Biochemistry
  • Structural Biology
  • Microbiology

Background:

  • Class D β-lactamases are crucial enzymes conferring antibiotic resistance by degrading β-lactam antibiotics.
  • Previous research has advanced understanding of their mechanisms and specificity through molecular biology and structural analysis.
  • Inconsistent residue numbering and secondary structure annotations hinder data comparison and interpretation across studies.

Purpose of the Study:

  • To introduce SAND (Standardized ANnotation system for beta-lactamase Domains), a novel naming system for residues and secondary structures.
  • To establish a unified framework for class D β-lactamase data, facilitating cross-study comparisons and interpretation.
  • To enable efficient data mining using AI-driven natural language processing (NLP) for accelerated research.

Main Methods:

  • Comprehensive structural alignment of all documented class D β-lactamase sequences.
  • Inclusion of experimentally obtained crystal structures for accurate annotation.
  • Development of a standardized naming convention for residues and secondary structure elements.

Main Results:

  • A proposed standardized naming system (SAND) for class D β-lactamase residues and secondary structures.
  • A unified framework that addresses inconsistencies in current annotation practices.
  • Facilitation of direct comparison and enhanced interpretation of diverse β-lactamase data.

Conclusions:

  • The SAND system provides a crucial tool for standardizing class D β-lactamase research.
  • This standardization will streamline data integration and interpretation, accelerating the discovery of new insights.
  • The framework is expected to enhance AI-driven analysis of scientific literature, speeding up advancements in antibiotic resistance research.