Literature DB >> 23215161

The state of the human proteome in 2012 as viewed through PeptideAtlas.

Terry Farrah1, Eric W Deutsch, Michael R Hoopmann, Janice L Hallows, Zhi Sun, Chung-Ying Huang, Robert L Moritz.   

Abstract

The Human Proteome Project was launched in September 2010 with the goal of characterizing at least one protein product from each protein-coding gene. Here we assess how much of the proteome has been detected to date via tandem mass spectrometry by analyzing PeptideAtlas, a compendium of human derived LC-MS/MS proteomics data from many laboratories around the world. All data sets are processed with a consistent set of parameters using the Trans-Proteomic Pipeline and subjected to a 1% protein FDR filter before inclusion in PeptideAtlas. Therefore, PeptideAtlas contains only high confidence protein identifications. To increase proteome coverage, we explored new comprehensive public data sources for data likely to add new proteins to the Human PeptideAtlas. We then folded these data into a Human PeptideAtlas 2012 build and mapped it to Swiss-Prot, a protein sequence database curated to contain one entry per human protein coding gene. We find that this latest PeptideAtlas build includes at least one peptide for each of ~12500 Swiss-Prot entries, leaving ~7500 gene products yet to be confidently cataloged. We characterize these "PA-unseen" proteins in terms of tissue localization, transcript abundance, and Gene Ontology enrichment, and propose reasons for their absence from PeptideAtlas and strategies for detecting them in the future.

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Year:  2012        PMID: 23215161      PMCID: PMC3928036          DOI: 10.1021/pr301012j

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  55 in total

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4.  Protein identification false discovery rates for very large proteomics data sets generated by tandem mass spectrometry.

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Review 5.  Targeted proteomic strategy for clinical biomarker discovery.

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Review 6.  A guided tour of the Trans-Proteomic Pipeline.

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Journal:  Proteomics       Date:  2010-03       Impact factor: 3.984

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Review 9.  Location, location, location...site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling.

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Journal:  Trends Pharmacol Sci       Date:  2008-07-06       Impact factor: 14.819

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Journal:  Genome Biol       Date:  2009-11-17       Impact factor: 13.583

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  50 in total

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Review 2.  The Structural and Functional Diversity of Intrinsically Disordered Regions in Transmembrane Proteins.

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Journal:  J Membr Biol       Date:  2019-05-28       Impact factor: 1.843

3.  Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources.

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Review 4.  Trans-Proteomic Pipeline, a standardized data processing pipeline for large-scale reproducible proteomics informatics.

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Journal:  Proteomics Clin Appl       Date:  2015-04-02       Impact factor: 3.494

5.  MOPED enables discoveries through consistently processed proteomics data.

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Journal:  J Proteome Res       Date:  2013-12-18       Impact factor: 4.466

6.  AP-SWATH Reveals Direct Involvement of VCP/p97 in Integrated Stress Response Signaling Through Facilitating CReP/PPP1R15B Degradation.

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Journal:  Mol Cell Proteomics       Date:  2018-03-29       Impact factor: 5.911

7.  Mass Spectrometry-Based Plasma Proteomics: Considerations from Sample Collection to Achieving Translational Data.

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Journal:  J Proteome Res       Date:  2019-10-11       Impact factor: 4.466

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9.  Plasma proteomics, the Human Proteome Project, and cancer-associated alternative splice variant proteins.

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10.  Metrics for the Human Proteome Project 2013-2014 and strategies for finding missing proteins.

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Journal:  J Proteome Res       Date:  2013-12-23       Impact factor: 4.466

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