Demo Data from EDBT 2026 / reviewers in the wild / expert
Daria V. Dibrova
dblp:70/8322
· DBLP profile ↗
1ranked-venue papers
1as first author
0since 2021 · last 2010
0000-0002-6954-6437ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
microbial genomics |
0.1 | 1 | 2010 | Characterization of the N-ATPase, a distinct, laterally transferred Na+-translocating form of the bacterial F-type membrane ATPase · Bioinform. 2010 |
Bioinformatics and computational biology › molecular evolution
horizontal gene transfer |
0.0 | 1 | 2010 | Characterization of the N-ATPase, a distinct, laterally transferred Na+-translocating form of the bacterial F-type membrane ATPase · Bioinform. 2010 |
Bioinformatics and computational biology
molecular evolution |
0.0 | 1 | 2010 | Characterization of the N-ATPase, a distinct, laterally transferred Na+-translocating form of the bacterial F-type membrane ATPase · Bioinform. 2010 |
Methods — techniques the papers use, named apart from their topics
phylogenetic analysis · 0.1genome comparison · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2010 | Characterization of the N-ATPase, a distinct, laterally transferred Na+-translocating form of the bacterial F-type membrane ATPaseabstractUNLABELLED: An analysis of the distribution of the Na(+)-translocating ATPases/ATP synthases among microbial genomes identified an atypical form of the F(1)F(o)-type ATPase that is present in the archaea Methanosarcina barkeri and M. acetivorans, in a number of phylogenetically diverse marine and halotolerant bacteria and in pathogens Burkholderia spp. In complete genomes, representatives of this form (referred to here as N-ATPase) are always present as second copies, in addition to the typical proton-translocating ATP synthases. The N-ATPase is encoded by a highly conserved atpDCQRBEFAG operon and its subunits cluster separately from the equivalent subunits of the typical F-type ATPases. N-ATPase c subunits carry a full set of sodium-binding residues, indicating that most of these enzymes are Na(+)-translocating ATPases that likely confer on their hosts the ability to extrude Na(+) ions. Other distinctive properties of the N-ATPase operons include the absence of the delta subunit from its cytoplasmic sector and the presence of two additional membrane subunits, AtpQ (formerly gene 1) and AtpR (formerly gene X). We argue that N-ATPases are an early-diverging branch of membrane ATPases that, similarly to the eukaryotic V-type ATPases, do not synthesize ATP. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Daria V. Dibrova, Michael Y. Galperin, Armen Y. Mulkidjanian |
Bioinform. | 1 |