Return
MatrixDB, the extracellular matrix interaction database
DOI:10.1093/nar/gkq830.png)
Abstract
En 中文
MatrixDB (http://matrixdb.ibcp.fr) is a freely available database focused on interactions established by extracellular proteins and polysaccharides. Only few databases report protein-polysaccharide interactions and, to the best of our knowledge, there is no other database of extracellular interactions. MatrixDB takes into account the multimeric nature of several extracellular protein families for the curation of interactions, and reports interactions with individual polypeptide chains or with multimers, considered as permanent complexes, when appropriate. MatrixDB is a member of the International Molecular Exchange consortium (IMEx) and has adopted the PSI-MI standards for the curation and the exchange of interaction data. MatrixDB stores experimental data from our laboratory, data from literature curation, data imported from IMEx databases, and data from the Human Protein Reference Database. MatrixDB is focused on mammalian interactions, but aims to integrate interaction datasets of model organisms when available. MatrixDB provides direct links to databases recapitulating mutations in genes encoding extracellular proteins, to UniGene and to the Human Protein Atlas that shows expression and localization of proteins in a large variety of normal human tissues and cells. MatrixDB allows researchers to perform customized queries and to build tissue- and disease-specific interaction networks that can be visualized and analyzed with Cytoscape or Medusa.
Keywords:
I COLLAGEN
PROTEIN
DISEASES
CELL
AI Summary
Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.
Journal
IF:
13.1
Papers:
3.6W
Citations:
29.0W
Organization
Cited Papers
KEGG for representation and analysis of molecular networks involving diseases and drugs
NUCLEIC ACIDS RESEARCH
IF13.1
COLdb, a Database Linking Genetic Data to Molecular Function in Fibrillar Collagens
HUMAN MUTATION
IF3.7
Consortium for osteogeneslis imperfecta mutations in the helical domain of type I collagen:: Regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans
HUMAN MUTATION
IF3.7
The minimum information required for reporting a molecular interaction experiment (MIMIx)
NATURE BIOTECHNOLOGY
IF41.7

