4.7 Article

PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 21, Issue 3, Pages 1069-1079

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbz050

Keywords

post-translational modifications; mutation; functional impact; database; Bioinformatics

Funding

  1. National Health and Medical Research Council of Australia (NHMRC) [1144652, 1127948]
  2. Australian Research Council (ARC) [LP110200333, DP120104460]
  3. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [R01 AI111965]
  4. Monash Major Inter-Disciplinary Research (IDR)
  5. Key Research and Development Program of Shaanxi Province, China [2017GY-197]
  6. Fundamental Research Funds for the Central Universities [3132019175]
  7. Informatics Institute of the School of Medicine at UAB
  8. National Health and Medical Research Council of Australia [1144652, 1127948] Funding Source: NHMRC

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Post-translational modifications (PTMs) play very important roles in various cell signaling pathways and biological process. Due to PTMs' extremely important roles, many major PTMs have been studied, while the functional and mechanical characterization of major PTMs is well documented in several databases. However, most currently available databases mainly focus on protein sequences, while the real 3D structures of PTMs have been largely ignored. Therefore, studies of PTMs 3D structural signatures have been severely limited by the deficiency of the data. Here, we develop PRISMOID, a novel publicly available and free 3D structure database for a wide range of PTMs. PRISMOID represents an up-to-date and interactive online knowledge base with specific focus on 3D structural contexts of PTMs sites and mutations that occur on PTMs and in the close proximity of PTM sites with functional impact. The first version of PRISMOID encompasses 17 145 non-redundant modification sites on 3919 related protein 3D structure entries pertaining to 37 different types of PTMs. Our entry web page is organized in a comprehensive manner, including detailed PTM annotation on the 3D structure and biological information in terms of mutations affecting PTMs, secondary structure features and per-residue solvent accessibility features of PTM sites, domain context, predicted natively disordered regions and sequence alignments. In addition, high-definition JavaScript packages are employed to enhance information visualization in PRISMOID. PRISMOID equips a variety of interactive and customizable search options and data browsing functions; these capabilities allow users to access data via keyword, ID and advanced options combination search in an efficient and user-friendly way. A download page is also provided to enable users to download the SQL file, computational structural features and PTM sites' data. We anticipate PRISMOID will swiftly become an invaluable online resource, assisting both biologists and bioinformaticians to conduct experiments and develop applications supporting discovery efforts in the sequence-structural-functional relationship of PTMs and providing important insight into mutations and PTM sites interaction mechanisms. The PRISMOID database is freely accessible at http://prismoid.erc.monash.edu/. The database and web interface are implemented in MySQL, JSP, JavaScript and HTML with all major browsers supported.

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