| Accession | ARO:3000005 |
| CARD Short Name | vanD |
| Definition | VanD is a D-Ala-D-Ala ligase homolog similar to VanA, and can synthesize D-Ala-D-Lac, an alternative substrate for peptidoglycan synthesis that reduces vancomycin binding affinity. It is associated with both vancomycin and teicoplanin resistance. |
| AMR Gene Family | Van ligase, glycopeptide resistance gene cluster |
| Drug Class | glycopeptide antibiotic |
| Resistance Mechanism | antibiotic target alteration |
| Resistomes with Perfect Matches | Enterococcus faeciumwgs |
| Resistomes with Sequence Variants | Blautia productawgs, Enterocloster clostridioformisg+wgs, Enterococcus faecalisg+wgs, Enterococcus faeciumg+wgs, Ruthenibacterium lactatiformanswgs |
| Classification | 14 ontology terms | Show + process or component of antibiotic biology or chemistry + mechanism of antibiotic resistance + antibiotic target alteration [Resistance Mechanism] + restructuring of bacterial cell wall conferring antibiotic resistance + determinant of antibiotic resistance + protein(s) conferring antibiotic resistance via molecular bypass + antibiotic molecule + gene(s) or protein(s) associated with a glycopeptide resistance cluster + glycopeptide antibiotic [Drug Class] + antibiotic resistance gene cluster, cassette, or operon + Van ligase [AMR Gene Family] + glycopeptide resistance gene cluster [AMR Gene Family] + teicoplanin [Antibiotic] + vancomycin [Antibiotic] |
| Parent Term(s) | 2 ontology terms | Show |
| Publications | Casadewall B and Courvalin P. 1999. J Bacteriol 181(12): 3644-3648. Characterization of the vanD glycopeptide resistance gene cluster from Enterococcus faecium BM4339. (PMID 10368136) |
Prevalence of vanD among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 414 important pathogens (see methodological details and complete list of analyzed pathogens). Values reflect percentage of genomes, plasmids, genome islands, or whole-genome shotgun assemblies that have at least one hit to the AMR detection model. Default view includes percentages calculated based on Perfect plus Strict RGI hits. Select the checkbox to view percentages based on only Perfect matches to AMR reference sequences curated in CARD (note: this excludes resistance via mutation as references in protein variant models are often wild-type, sensitive sequences).
| Species | NCBI Chromosome | NCBI Plasmid | NCBI WGS | NCBI GI | GRDI-AMR2 |
|---|---|---|---|---|---|
| Blautia producta | 0% | 0% | 18.18% | 0% | 0% |
| Enterocloster clostridioformis | 100% | 0% | 53.49% | 0% | 0% |
| Enterococcus faecalis | 0.91% | 0% | 0.08% | 0% | 0% |
| Enterococcus faecium | 0.96% | 0% | 0.48% | 0% | 0% |
| Ruthenibacterium lactatiformans | 0% | 0% | 3.33% | 0% | 0% |
Model Type: protein homolog model
Model Definition: Protein Homolog Models (PHM) detect protein sequences based on their similarity to a curated reference sequence, using curated BLASTP bitscore cut-offs. Protein Homolog Models apply to all genes that confer resistance through their presence in an organism, such as the presence of a beta-lactamase gene on a plasmid. PHMs include a reference sequence and a bitscore cut-off for detection using BLASTP. A Perfect RGI match is 100% identical to the reference protein sequence along its entire length, a Strict RGI match is not identical but the bit-score of the matched sequence is greater than the curated BLASTP bit-score cutoff, Loose RGI matches have a bit-score less than the curated BLASTP bit-score cut-off.
Bit-score Cut-off (blastP): 350
| Curator | Description | Most Recent Edit |
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