{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,14]],"date-time":"2026-02-14T02:40:24Z","timestamp":1771036824456,"version":"3.50.1"},"reference-count":16,"publisher":"Oxford University Press (OUP)","issue":"19","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Summary: Domain mapping of disease mutations (DMDM) is a database in which each disease mutation can be displayed by its gene, protein or domain location. DMDM provides a unique domain-level view where all human coding mutations are mapped on the protein domain. To build DMDM, all human proteins were aligned to a database of conserved protein domains using a Hidden Markov Model-based sequence alignment tool (HMMer). The resulting protein-domain alignments were used to provide a domain location for all available human disease mutations and polymorphisms. The number of disease mutations and polymorphisms in each domain position are displayed alongside other relevant functional information (e.g. the binding and catalytic activity of the site and the conservation of that domain location). DMDM's protein domain view highlights molecular relationships among mutations from different diseases that might not be clearly observed with traditional gene-centric visualization tools.<\/jats:p>\n               <jats:p>Availability: Freely available at http:\/\/bioinf.umbc.edu\/dmdm<\/jats:p>\n               <jats:p>Contact: \u00a0mkann@umbc.edu<\/jats:p>","DOI":"10.1093\/bioinformatics\/btq447","type":"journal-article","created":{"date-parts":[[2010,8,5]],"date-time":"2010-08-05T03:27:36Z","timestamp":1280978856000},"page":"2458-2459","source":"Crossref","is-referenced-by-count":52,"title":["DMDM: domain mapping of disease mutations"],"prefix":"10.1093","volume":"26","author":[{"given":"Thomas A.","family":"Peterson","sequence":"first","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Asa","family":"Adadey","sequence":"additional","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ivette","family":"Santana-Cruz","sequence":"additional","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yanan","family":"Sun","sequence":"additional","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew","family":"Winder","sequence":"additional","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maricel G.","family":"Kann","sequence":"additional","affiliation":[{"name":"1Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2010,8,4]]},"reference":[{"key":"2023012508171223500_B1","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1093\/nar\/gkg095","article-title":"The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003","volume":"31","author":"Boeckmann","year":"2003","journal-title":"Nucleic Acids Res."},{"key":"2023012508171223500_B2","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1007\/s00018-004-4416-1","article-title":"The evolution of domain arrangements in proteins and interaction networks","volume":"62","author":"Bornberg-Bauer","year":"2005","journal-title":"Cell. 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