| URL: | https://tbdb.io |
| Full name: | T-box Riboswitch Annotation Database |
| Description: | The T-box riboswitch annotation database (TBDB) is a database that attempts to annotate structural and genetic features of T-box leader sequences. The goal of this database is to enrich information available about T-box riboswitch sequences in order to facilitate research in this area. While >15,000 T-box riboswitch sequences have been discovered by genome mining, only a handful have been experimentally characterized. We hope that the information contained in this database will decrease the barrier to entry into this field. |
| Year founded: | 2021 |
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| Version: | |
| Accessibility: |
Accessible
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| Country/Region: | United States |
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| University/Institution: | Harvard University |
| Address: | Boston, MA 02115, USA |
| City: | Boston |
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| Country/Region: | United States |
| Contact name (PI/Team): | George M Church |
| Contact email (PI/Helpdesk): | gchurch@genetics.med.harvard.edu |
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TBDB: a database of structurally annotated T-box riboswitch:tRNA pairs. [PMID: 32882008]
T-box riboswitches constitute a large family of tRNA-binding leader sequences that play a central role in gene regulation in many gram-positive bacteria. Accurate inference of the tRNA binding to T-box riboswitches is critical to predict their cis-regulatory activity. However, there is no central repository of information on the tRNA binding specificities of T-box riboswitches, and de novo prediction of binding specificities requires advanced knowledge of computational tools to annotate riboswitch secondary structure features. Here, we present the T-box Riboswitch Annotation Database (TBDB, https://tbdb.io), an open-access database with a collection of 23,535 T-box riboswitch sequences, spanning the major phyla of 3,632 bacterial species. Among structural predictions, the TBDB also identifies specifier sequences, cognate tRNA binding partners, and downstream regulatory targets. To our knowledge, the TBDB presents the largest collection of feature, sequence, and structural annotations carried out on this important family of regulatory RNA. |