GenomewidePDB 2.0: A Newly Upgraded Versatile Proteogenomic Database for the Chromosome-Centric Human Proteome Project

被引:8
|
作者
Jeong, Seul-Ki [1 ,2 ]
Hancock, William S. [3 ,4 ]
Paik, Young-Ki [1 ,2 ,5 ]
机构
[1] Yonsei Proteome Res Ctr, Seoul 120749, South Korea
[2] Biomed Proteome Res Ctr, Seoul 120749, South Korea
[3] Northeastern Univ, Barnett Inst, Boston, MA 02115 USA
[4] Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USA
[5] Yonsei Univ, Dept Integrated Omics Biomed Sci, World Class Univ, Dept Biochem,Grad Program, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
Chromosome-Centric Human Proteome Project; database; proteomics; alternative splicing; GenomewidePDB; missing protein; SPLICE VARIANTS; PROTEINS; KNOWLEDGEBASE; TISSUE; DRAFT;
D O I
10.1021/acs.jproteome.5b00541
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Since the launch of the Chromosome-centric Human Proteome Project (C-HPP) in 2012, the number of "missing" proteins has fallen to 2932, down from similar to 5932 since the number was first counted in 2011. We compared the characteristics of missing proteins with those of already annotated proteins with respect to transcriptional expression pattern and the time periods in which newly identified proteins were annotated. We learned that missing proteins commonly exhibit lower levels of transcriptional expression and less tissue-specific expression compared with already annotated proteins. This makes it more difficult to identify missing proteins as time goes on. One of the C-HPP goals is to identify alternative spliced product of proteins (ASPs), which are usually difficult to find by shot-gun proteomic methods due to their sequence similarities with the representative proteins. To resolve this problem, it may be necessary to use a targeted proteomics approach (e.g., selected and multiple reaction monitoring [S/MRM] assays) and an innovative bioinformatics platform that enables the selection of target peptides for rarely expressed missing proteins or ASPs. Given that the success of efforts to identify missing proteins may rely on more informative public databases, it was necessary to upgrade the available integrative databases. To this end, we attempted to improve the features and utility of GenomewidePDB by integrating transcriptomic information (e.g., alternatively spliced transcripts), annotated peptide information, and an advanced search interface that can find proteins of interest when applying a targeted proteomics strategy. This upgraded version of the database, GenomewidePDB 2.0, may not only expedite identification of the remaining missing proteins but also enhance the exchange of information among the proteome community. GenomewidePDB 2.0 is available publicly at http://genomewidepdb.proteomix.org/.
引用
收藏
页码:3710 / 3719
页数:10
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