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Anna Maria Gallina

dblp:125/7431 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2013
—ORCID · none

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › structural bioinformatics
protein-ligand interaction analysis
0.212013
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
0.012013
PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures · Bioinform. 2013
Bioinformatics and computational biology
structural bioinformatics
0.012013
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
YearPublicationVenuePosition
2013 PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures
abstract
MOTIVATION: 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.1