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.
DOI: 10.1039/c1mb05420a
PMID: 22134333