Standardized Residue Numbering and Secondary Structure Nomenclature in the Class D β-Lactamases

Over 1370 class D β-lactamases are currently known, and they pose a serious threat to the effective treatment of many infectious diseases, particularly in some pathogenic bacteria where evolving carbapenemase activity has been reported. Detailed understanding of their molecular biology, enzymology, and structural biology are critically important, but the lack of a standardized residue numbering scheme and inconsistent secondary structure annotation has made comparative analyses sometimes difficult and cumbersome. Compounding this, in the post-AlphaFold world where we currently find ourselves, an extraordinary wealth of detailed structural information on these enzymes is literally at our fingertips; therefore it is vitally important that a standard numbering system is in place to facilitate the accurate and straightforward analysis of their structures. Here we present a residue numbering and secondary structure scheme for the class D enzymes based on the sequence and structure of OXA-48 and apply it to test targets to demonstrate the ease with which it can be used.

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Publication Details

Journal
ACS Infectious Diseases
Published
2025-03-17
DOI
https://doi.org/10.1021/acsinfecdis.5c00060
Citations
4
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
2.36

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article

Standardized Residue Numbering and Secondary Structure Nomenclature in the Class D β-Lactamases

Clyde A. Smith, Anastasiya Stasyuk
4 citations
ACS Infectious Diseases
Antibiotic Resistance in Bacteria
2.36
article

Standardized Residue Numbering and Secondary Structure Nomenclature in the Class D β-Lactamases

Clyde A. Smith, Anastasiya Stasyuk
article en
4 citations

Abstract

Over 1370 class D β-lactamases are currently known, and they pose a serious threat to the effective treatment of many infectious diseases, particularly in some pathogenic bacteria where evolving carbapenemase activity has been reported. Detailed understanding of their molecular biology, enzymology, and structural biology are critically important, but the lack of a standardized residue numbering scheme and inconsistent secondary structure annotation has made comparative analyses sometimes difficult and cumbersome. Compounding this, in the post-AlphaFold world where we currently find ourselves, an extraordinary wealth of detailed structural information on these enzymes is literally at our fingertips; therefore it is vitally important that a standard numbering system is in place to facilitate the accurate and straightforward analysis of their structures. Here we present a residue numbering and secondary structure scheme for the class D enzymes based on the sequence and structure of OXA-48 and apply it to test targets to demonstrate the ease with which it can be used.

ACS Infectious DiseasesVol. 11(4)
SLAC National Accelerator Laboratory (US), Stanford Synchrotron Radiation Lightsource (US), Stanford University (US)
Office of Science, National Institute of General Medical Sciences, Biological and Environmental Research
Zero hunger
Openalex Percentile: Top 12%
Antibiotic Resistance in Bacteria
2.36
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