Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009:2009:bap004.
doi: 10.1093/database/bap004. Epub 2009 Apr 17.

The Homeodomain Resource: a comprehensive collection of sequence, structure, interaction, genomic and functional information on the homeodomain protein family

Affiliations

The Homeodomain Resource: a comprehensive collection of sequence, structure, interaction, genomic and functional information on the homeodomain protein family

R Travis Moreland et al. Database (Oxford). 2009.

Abstract

The Homeodomain Resource is a curated collection of sequence, structure, interaction, genomic and functional information on the homeodomain family. The current version builds upon previous versions by the addition of new, complete sets of homeodomain sequences from fully sequenced genomes, the expansion of existing curated homeodomain information and the improvement of data accessibility through better search tools and more complete data integration. This release contains 1534 full-length homeodomain-containing sequences, 93 experimentally derived homeodomain structures, 101 homeodomain protein-protein interactions, 107 homeodomain DNA-binding sites and 206 homeodomain proteins implicated in human genetic disorders.Database URL: The Homeodomain Resource is freely available and can be accessed at http://research.nhgri.nih.gov/homeodomain/

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
HDR relational framework. The relational design connecting the Homeodomain Resource's 14 primary tables are illustrated in the figure. Primary keys are indicated in red, foreign keys in green and keys characterized as both primary and foreign in blue. The new database design is centered around data found in the ‘Proteins’ table. All proteins are lineage-specific and linked to the ‘Organisms’ table. A single protein may contain one or more homeodomains related to the ‘Proteins_Homeodomains’ table. DNA-binding targets, protein–protein interactions, 3D structures and homeodomains implicated in human disorders are normalized and linked to the ‘Proteins’ table. External annotation from multiple databases are integrated via the ‘External_Ids’ table. Database entries are referenced with their primary citation via the ‘Publications’ table.
Figure 2.
Figure 2.
The Homeodomain Resource provides a simple search query interface, allowing the user to either query part or all of the Resource (top). Selecting ‘Entire Database’ from the pull-down menu returns a summary screen, indicating how many entries of each type were identified (bottom). Clicking on any of the hyperlinked numbers in the table takes the user directly to that set of results. In addition, overall navigation within the site has been improved with the addition of sidebar tools and links to complete datasets in each homeodomain category.
Figure 3.
Figure 3.
Search results from a query of protein–protein interactions data for the interaction of homeodomain proteins Lhx2 and Msx1 (SEARCH ‘Protein-Protein Interactions’ FOR ‘MSX1’) (top). Each protein–protein interaction entry within the Homeodomain Resource is hyperlinked to the corresponding entry in BIND, which provides additional details on the mechanism(s) of interaction (bottom). See text for additional details.

Similar articles

Cited by

References

    1. Gehring WJ, Affolter M, Burglin T. Homeodomain proteins. Annu. Rev. Biochem. 1994;63:487–526. - PubMed
    1. Ceska TA, Lamers M, Monaci P, et al. The X-ray structure of an atypical homeodomain present in the rat liver transcription factor LFB1/HNF1 and implications for DNA binding. EMBO J. 1993;12:1805–1810. - PMC - PubMed
    1. Dekker N, Cox M, Boelens R, et al. Solution structure of the POU-specific DNA-binding domain of Oct-1. Nature. 1993;362:852–855. - PubMed
    1. Endo T, Ohta K, Saito T, et al. Structure of the rat thyroid transcription factor-1 (TTF-1) gene. Biochem. Biophys. Res. Commun. 1994;204:1358–1363. - PubMed
    1. Kissinger CR, Liu BS, Martin-Blanco E, et al. Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions. Cell. 1990;63:579–590. - PubMed