Related Experiment Video
Updated: Jun 8, 2026

08:06
The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
Published on: February 1, 2018
SHV Lactamase Engineering Database: a reconciliation tool for SHV β-lactamases in public databases
1Institute of Technical Biochemistry, University of Stuttgart, Allmandring 31, 70569 Stuttgart, Germany.
BMC Genomics
|October 15, 2010
Summary
The SHV β-Lactamase Engineering Database (SHVED) consolidates SHV variant data from multiple sources. This resource aids in identifying new mutations and understanding antibiotic resistance mechanisms.
Area of Science:
- Microbiology
- Structural Biology
- Bioinformatics
Background:
- SHV β-lactamases are enzymes conferring antibiotic resistance through accumulating mutations.
- The number of known SHV variants is rapidly increasing, with 117 variants in the SHV mutation table.
- Information on SHV β-lactamases is available in the NCBI protein database, but inconsistencies exist.
Purpose of the Study:
- To develop the SHV β-Lactamase Engineering Database (SHVED) for collecting and reconciling SHV β-lactamase sequence data.
- To provide a centralized resource for identifying new SHV variants and amino acid substitutions.
- To detect and resolve inconsistencies in existing databases.
Main Methods:
- Collected SHV β-lactamase sequences from the NCBI protein database and the SHV mutation table.
- Developed the SHVED to store 200 distinct protein entries and 20 crystal structures.
- Reconciled 27 protein entries with inconsistent SHV name identification using data from the SHV mutation table.
Main Results:
- The SHVED contains 200 distinct protein entries and 20 crystal structures.
- Identified 82 sequences unique to the NCBI protein database, including 22 unclassified full-length sequences.
- Resolved inconsistencies in SHV naming conventions by cross-referencing with the SHV mutation table.
Conclusions:
- The SHVED provides reconciled annotation for SHV variants, enhancing data accuracy.
- Facilitates the detection of inconsistencies within the NCBI protein database.
- Supports the identification of novel mutations and SHV variants, aiding in the study of sequence-function relationships.
