Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces
Radboud University Medical Center · Radboud University Nijmegen · +3 more institutions
Abstract
Many newly detected point mutations are located in protein-coding regions of the human genome. Knowledge of their effects on the protein's 3D structure provides insight into the protein's mechanism, can aid the design of further experiments, and eventually can lead to the development of new medicines and diagnostic tools.
In this article we describe HOPE, a fully automatic program that analyzes the structural and functional effects of point mutations. HOPE collects information from a wide range of information sources including calculations on the 3D coordinates of the protein by using WHAT IF Web services, sequence annotations from the UniProt database, and predictions by DAS services. Homology models are built with YASARA. Data is stored in a database and used in a decision scheme to identify the effects of a mutation on the protein's 3D structure and function. HOPE builds a report with text, figures, and animations that is easy to use and understandable for (bio)medical researchers.
Citation impact
- FWCI
- 11.05
- Percentile
- 100%
- References
- 27
Authors
5- HVHanka VenselaarCorresponding
Radboud University Medical Center, Radboud University Nijmegen
- TATim AH te Beek
Netherlands Bioinformatics Centre
- RKRemko Kuipers
Bio-Prodict (Netherlands), Wageningen University & Research
- MLMaarten L. Hekkelman
Radboud University Nijmegen, Radboud University Medical Center
- GVGert Vriend
Radboud University Medical Center, Radboud University Nijmegen
Topics & keywords
- UniProt
- Computer science
- Coding (social sciences)
- Protein structure database
- Structural bioinformatics
- Biological database
- Computational biology
- Protein structure