iLoc-Cell

iLoc-Cell predicts the subcellular localization of human proteins, including proteins that occupy multiple distinct subcellular sites.


Key Features:

  • Multiplex Localization Prediction: Identifies both single-location and multiple-location assignments for human proteins, addressing proteins that occupy two or more subcellular sites.
  • Comprehensive Coverage: Covers 14 subcellular sites: centrosome, cytoplasm, cytoskeleton, endoplasmic reticulum, endosome, extracellular space, Golgi apparatus, lysosome, microsome, mitochondrion, nucleus, peroxisome, plasma membrane, and synapse.
  • High Accuracy: Achieved an overall success rate of 76% in jackknife cross-validation on datasets containing proteins assigned to two, three, or four locations, with subsets constrained to no more than 25% pairwise sequence identity.
  • Independent Validation: Performance was confirmed using two independent datasets, with success rates reported as superior to existing predictors capable of handling multi-location proteins.

Scientific Applications:

  • Functional Genomics: Facilitates assignment of proteins to cellular compartments to infer functional roles within cellular contexts.
  • Protein Engineering and Drug Design: Provides subcellular localization information useful for targeting or modifying proteins for therapeutic or engineering purposes.
  • Cell Biology Research: Supports studies of cellular dynamics and interactions by mapping proteins to their respective cellular sites.

Methodology:

Benchmark tests employed jackknife cross-validation on datasets of proteins annotated with two, three, or four locations (with ≤25% pairwise sequence identity within subsets) and validation was performed on two independent datasets.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Chou K, Wu Z, Xiao X. iLoc-Hum: using the accumulation-label scale to predict subcellular locations of human proteins with both single and multiple sites. Mol. BioSyst.. 2012;8(2):629-641. doi:10.1039/c1mb05420a. PMID:22134333.

Documentation

Links