Predicting subcellular localization of proteins based on their N-terminal amino acid sequence.
By Olof Emanuelsson, Henrik Nielsen, Søren Brunak, G. von Heijne. Journal of Molecular Biology, 2000
4,387 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/bebaee82a5d98dd4b7cd2b41f669fec74c243f48
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Citations in the corpus
- Cell-PLoc 2.0: an improved package of web-servers for predicting subcellular localization of proteins in various organisms (2010, methodology): “For instance, the cutoff threshold to reduce the homology bias for the benchmark dataset used in Predotar [111] was set at 80%, meaning that only those sequences which have 80% pairwise sequence identity to any other in a same subset were excluded [111]; while for the benchmark dataset used in Tar”
- Comparing function and structure between entire proteomes (2001, background): “The following results are based on predictions that may be wrong.”
- Prediction of protein subcellular localization (2006, background): “The most used features are the short N-terminal amino acid sequences[6, 7, 14-16] (i.”
- iLoc-Euk: A Multi-Label Classifier for Predicting the Subcellular Localization of Singleplex and Multiplex Eukaryotic Proteins (2011, background): “, [11,12,13,14,15,16,17,18,19,20,21,22,23,24] as well as a long list”
- Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004, neutral): “Green boxes show internal viewers for the results of clustering (Clustering Viewer showing results by H-Inv, STACK, TIGR, UniGene, etc.), the prediction of subcellular localization (TOPOViewer showing results of TMHMM, SOSUI, TargetP, and PsortII), and the disease-related information (DiseaseInfo Vi”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, positive): “, 2004) and TargetP (Emanuelsson et al., 2000) clearly assigned PPR8522 to the chloroplast, and the SignalP (Emanuelsson et al.”
- IRT1, an Arabidopsis Transporter Essential for Iron Uptake from the Soil and for Plant Growth Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.001388. (2002, background): “IRT1 Is a Plasma Membrane Transporter The PsortI (Nakai and Kanehisa, 1992) and TargetP (Emanuelsson et al., 2000) programs predicted a plasma membrane localization of the IRT1 protein.”
- Predicting subcellular localization of proteins using machine-learned classifiers (2004, background): “Name Acc Coverage Technique PSORT-B .75 1443 GN bacterial combination LOCkey .87 1161 assorted homology .91 291 prokaryotic SubLoc .79 2427 eukaryotic AA composition .85 940 plantTargetP .90 2738 non-plant signal prediction .93 16284 animal .93 3420 plant .81 2104 fungal .92 3218 GN bacterial Proteo”
- Locating proteins in the cell using TargetP, SignalP and related tools (2007, background): “A successor of ChloroP is TargetP, which provides prediction of cTPs, mTPs and secretory SP”
- SUBA3: a database for integrating experimentation and prediction to define the SUBcellular location of proteins in Arabidopsis (2012, background): “These bioinformatic programs have become increasingly important for annotating newly sequenced genes and for providing testable hypotheses regarding protein localization and function (5).”
- MultiLoc2: integrating phylogeny and Gene Ontology terms improves subcellular protein localization prediction (2009, methodology): “The MultiLoc2 approach was compared with current stateof-the-art tools (BaCelLo [19], LOCtree [2], Protein Prowler [9], TargetP [5] and WoLF PSORT [22]) using independent datasets sharing very low sequence identity with the training datasets of all compared tools.”
- Better prediction of sub‐cellular localization by combining evolutionary and structural information (2003, methodology): “Additional methods: PSORT II: knowledge-based expert system using amino acid composition and sequence motifs, 46, (20); TargetP: combined method predicting extra-cellular (SignalP), chloroplast (ChloroP) and mitochondrial proteins.(21) Significant differences: For our networks the standard deviation”