pr0c00485_si_003.xls (501 kB)
Download fileResearch on the Human Proteome Reaches a Major Milestone: >90% of Predicted Human Proteins Now Credibly Detected, According to the HUPO Human Proteome Project
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posted on 2020-10-16, 17:39 authored by Gilbert S. Omenn, Lydie Lane, Christopher M. Overall, Ileana M. Cristea, Fernando J. Corrales, Cecilia Lindskog, Young-Ki Paik, Jennifer E. Van Eyk, Siqi Liu, Stephen R. Pennington, Michael P. Snyder, Mark S. Baker, Nuno Bandeira, Ruedi Aebersold, Robert L. Moritz, Eric W. DeutschAccording to the
2020 Metrics of the HUPO Human Proteome Project
(HPP), expression has now been detected at the protein level for >90%
of the 19 773 predicted proteins coded in the human genome.
The HPP annually reports on progress made throughout the world toward
credibly identifying and characterizing the complete human protein
parts list and promoting proteomics as an integral part of multiomics
studies in medicine and the life sciences. NeXtProt release 2020–01
classified 17 874 proteins as PE1, having strong protein-level
evidence, up 180 from 17 694 one year earlier. These represent
90.4% of the 19 773 predicted coding genes (all PE1,2,3,4 proteins
in neXtProt). Conversely, the number of neXtProt PE2,3,4 proteins,
termed the “missing proteins” (MPs), was reduced by
230 from 2129 to 1899 since the neXtProt 2019–01 release. PeptideAtlas
is the primary source of uniform reanalysis of raw mass spectrometry
data for neXtProt, supplemented this year with extensive data from
MassIVE. PeptideAtlas 2020–01 added 362 canonical proteins
between 2019 and 2020 and MassIVE contributed 84 more, many of which
converted PE1 entries based on non-MS evidence to the MS-based subgroup.
The 19 Biology and Disease-driven B/D-HPP teams continue to pursue
the identification of driver proteins that underlie disease states,
the characterization of regulatory mechanisms controlling the functions
of these proteins, their proteoforms, and their interactions, and
the progression of transitions from correlation to coexpression to
causal networks after system perturbations. And the Human Protein
Atlas published Blood, Brain, and Metabolic Atlases.