PhosphoELM database

PhosphoELM provides a relational database of experimentally verified phosphorylation sites in eukaryotic proteins to support studies of protein phosphorylation and its roles in cellular signaling.


Key Features:

  • Extensive data collection: Houses 42,574 non-redundant phosphorylation sites on serine, threonine, and tyrosine residues curated from in vivo and in vitro experiments and phosphoproteomic studies.
  • Enhanced data annotation: Annotates phosphosites with structural disorder/order information and residue accessibility.
  • Conservation analysis: Provides a conservation score for each phosphosite computed from multiple sequence alignments and a visualization overlay of conservation on those alignments.
  • Integration with external resources: Links phosphosites to external databases and protein–protein interaction networks to enable network-level analyses.

Scientific Applications:

  • Functional genomics: Interpreting the functional roles of phosphorylation in gene regulation and signal transduction pathways.
  • Proteomics research: Identifying phosphorylation sites as potential biomarkers or therapeutic targets in diseases such as cancer.
  • Structural biology: Investigating how phosphorylation affects protein structure, stability, and interactions.
  • Network analysis: Enabling protein–protein interaction and network analyses of phosphorylation-mediated signaling.

Methodology:

Stores curated phosphosite data in a relational database, computes conservation scores from multiple sequence alignments, and links entries to external databases and interaction networks.

Topics

Collections

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
10/7/2015
Last Updated:
4/13/2021

Operations

Data Inputs & Outputs

Other operations do not define inputs or outputs.

Publications

Dinkel H, Chica C, Via A, Gould CM, Jensen LJ, Gibson TJ, Diella F. Phospho.ELM: a database of phosphorylation sites--update 2011. Nucleic Acids Research. 2010;39(Database):D261-D267. doi:10.1093/nar/gkq1104. PMID:21062810. PMCID:PMC3013696.

Documentation