Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

TOPPR

General information

URL: http://iomics.ugent.be/toppr/
Full name: The Online Protein Processing Resource
Description: TOPPR is an online database that contains thousands of published proteolytically processed sites in human and mouse proteins.
Year founded: 2013
Last update: NA
Version:
Accessibility:
Accessible
Country/Region: Belgium

Classification & Tag

Data type:
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: Ghent University
Address: Department of Medical Protein Research,VIB,A. Baertsoenkaai 3,B-9000 Ghent,Belgium
City: Ghent
Province/State:
Country/Region: Belgium
Contact name (PI/Team): Kris Gevaert
Contact email (PI/Helpdesk): kris.gevaert@vib-ugent.be

Publications

23093603
The Online Protein Processing Resource (TOPPR): a database and analysis platform for protein processing events. [PMID: 23093603]
Colaert N, Maddelein D, Impens F, Van Damme P, Plasman K, Helsens K, Hulstaert N, Vandekerckhove J, Gevaert K, Martens L.

We here present The Online Protein Processing Resource (TOPPR; http://iomics.ugent.be/toppr/), an online database that contains thousands of published proteolytically processed sites in human and mouse proteins. These cleavage events were identified with COmbinded FRActional DIagonal Chromatography proteomics technologies, and the resulting database is provided with full data provenance. Indeed, TOPPR provides an interactive visual display of the actual fragmentation mass spectrum that led to each identification of a reported processed site, complete with fragment ion annotations and search engine scores. Apart from warehousing and disseminating these data in an intuitive manner, TOPPR also provides an online analysis platform, including methods to analyze protease specificity and substrate-centric analyses. Concretely, TOPPR supports three ways to retrieve data: (i) the retrieval of all substrates for one or more cellular stimuli or assays; (ii) a substrate search by UniProtKB/Swiss-Prot accession number, entry name or description; and (iii) a motif search that retrieves substrates matching a user-defined protease specificity profile. The analysis of the substrates is supported through the presence of a variety of annotations, including predicted secondary structure, known domains and experimentally obtained 3D structure where available. Across substrates, substrate orthologs and conserved sequence stretches can also be shown, with iceLogo visualization provided for the latter.

Nucleic Acids Res. 2013:41(Database issue) | 14 Citations (from Europe PMC, 2026-04-04)

Ranking

All databases:
4980/6932 (28.174%)
Pathway:
312/454 (31.498%)
4980
Total Rank
14
Citations
1.077
z-index

Community reviews

Not Rated
Data quality & quantity:
Content organization & presentation
System accessibility & reliability:

Word cloud

Related Databases

Citing
Cited by

Record metadata

Created on: 2015-06-20
Curated by:
Lina Ma [2018-07-04]
Mengwei Li [2016-02-16]
Guangyu Wang [2015-12-06]
Guangyu Wang [2015-06-26]