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PMID: 11125133 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Collecting and harvesting biological data: the GPCRDB and NucleaRDB information systems.

Nucleic acids research ·Vol. 29 ·No. 1 ·2001-01-01 ·Pages 346-9

Horn F, Vriend G, Cohen FE

Abstract

The amount of genomic and proteomic data that is entered each day into databases and the experimental literature is outstripping the ability of experimental scientists to keep pace. While generic databases derived from automated curation efforts are useful, most biological scientists tend to focus on a class or family of molecules and their biological impact. Consequently, there is a need for molecular class-specific or other specialized databases. Such databases collect and organize data around a single topic or class of molecules. If curated well, such systems are extremely useful as they allow experimental scientists to obtain a large portion of the available data most relevant to their needs from a single source. We are involved in the development of two such databases with substantial pharmacological relevance. These are the GPCRDB and NucleaRDB information systems, which collect and disseminate data related to G protein-coupled receptors and intra-nuclear hormone receptors, respectively. The GPCRDB was a pilot project aimed at building a generic molecular class-specific database capable of dealing with highly heterogeneous data. A first version of the GPCRDB project has been completed and it is routinely used by thousands of scientists. The NucleaRDB was started recently as an application of the concept for the generalization of this technology. The GPCRDB is available via the WWW at http://www.gpcr.org/7tm/ and the NucleaRDB at http://www.receptors.org/NR/.

MeSH Terms
Binding, Competitive Databases, Factual GTP-Binding Proteins/metabolism Information Storage and Retrieval Internet Ligands Mutation Receptors, Cell Surface/genetics,metabolism Receptors, Cytoplasmic and Nuclear/genetics Sequence Alignment
Chemicals
Ligands Receptors, Cell Surface Receptors, Cytoplasmic and Nuclear GTP-Binding Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Horn F
Department of Cellular and Molecular Pharmacology, UCSF, Box 0450, San Francisco, CA 94143-0450, USA. horn@cmpharm.ucsf.edu
Vriend G
Cohen F E
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
1362-4962
Published
2001-01-01
Pages
346-9
Language
English
Region
England
NLM ID
0411011
PMCID
PMC29816
Subset
IM
Analysis Services
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