EDBT 2026 Demo / reviewers in the wild / expert
Maurizio Bergamino
dblp:28/10470
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2013
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
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 › structural bioinformatics
protein-ligand interaction analysis |
0.2 | 1 | 2013 | PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures · Bioinform. 2013 |
Bioinformatics and computational biology › structural bioinformatics › protein structure database
protein structure database mining |
0.0 | 1 | 2013 | PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures · Bioinform. 2013 |
Bioinformatics and computational biology
structural bioinformatics |
0.0 | 1 | 2013 | PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures · Bioinform. 2013 |
Methods — techniques the papers use, named apart from their topics
web services · 0.2database curation · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2013 | PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structuresabstractMOTIVATION: A large fraction of the entries contained in the Protein Data Bank describe proteins in complex with low molecular weight molecules such as physiological compounds or synthetic drugs. In many cases, the same molecule is found in distinct protein-ligand complexes. There is an increasing interest in Medicinal Chemistry in comparing protein binding sites to get insight on interactions that modulate the binding specificity, as this structural information can be correlated with other experimental data of biochemical or physiological nature and may help in rational drug design. RESULTS: The web service protein-ligand interaction presented here provides a tool to analyse and compare the binding pockets of homologous proteins in complex with a selected ligand. The information is deduced from protein-ligand complexes present in the Protein Data Bank and stored in the underlying database. AVAILABILITY: Freely accessible at http://bioinformatics.istge.it/pli/. Anna Maria Gallina, Paola Bisignano, Maurizio Bergamino, Domenico Bordo |
Bioinform. | 3 |