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PhosphoPOINT: a comprehensive human kinase interactome and phospho-protein database.
- Source :
-
Bioinformatics (Oxford, England) [Bioinformatics] 2008 Aug 15; Vol. 24 (16), pp. i14-20. - Publication Year :
- 2008
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Abstract
- Motivation: To fully understand how a protein kinase regulates biological processes, it is imperative to first identify its substrate(s) and interacting protein(s). However, of the 518 known human serine/threonine/tyrosine kinases, 35% of these have known substrates, while 14% of the kinases have identified substrate recognition motifs. In contrast, 85% of the kinases have protein-protein interaction (PPI) datasets, raising the possibility that we might reveal potential kinase-substrate pairs from these PPIs.<br />Results: PhosphoPOINT, a comprehensive human kinase interactome and phospho-protein database, is a collection of 4195 phospho-proteins with a total of 15 738 phosphorylation sites. PhosphoPOINT annotates the interactions among kinases, with their down-stream substrates and with interacting (phospho)-proteins to modulate the kinase-substrate pairs. PhosphoPOINT implements various gene expression profiles and Gene Ontology cellular component information to evaluate each kinase and their interacting (phospho)-proteins/substrates. Integration of cSNPs that cause amino acids change with the proteins with the phosphoprotein dataset reveals that 64 phosphorylation sites result in a disease phenotypes when changed; the linked phenotypes include schizophrenia and hypertension. PhosphoPOINT also provides a search function for all phospho-peptides using about 300 known kinase/phosphatase substrate/binding motifs. Altogether, PhosphoPOINT provides robust annotation for kinases, their downstream substrates and their interaction (phospho)-proteins and this should accelerate the functional characterization of kinomemediated signaling.<br />Availability: PhosphoPOINT can be freely accessed in http://kinase. bioinformatics.tw/.<br />Supplementary Information: Supplementary data are available at Bioinformatics online.
- Subjects :
- Binding Sites
Humans
Information Storage and Retrieval methods
Phosphoproteins chemistry
Phosphorylation
Phosphotransferases chemistry
Protein Binding
Proteome chemistry
User-Computer Interface
Databases, Protein
Phosphoproteins metabolism
Phosphotransferases metabolism
Protein Interaction Mapping methods
Proteome metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1367-4811
- Volume :
- 24
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Bioinformatics (Oxford, England)
- Publication Type :
- Academic Journal
- Accession number :
- 18689816
- Full Text :
- https://doi.org/10.1093/bioinformatics/btn297