J
Jimmy K. Eng
Researcher at University of Washington
Publications - 171
Citations - 37832
Jimmy K. Eng is an academic researcher from University of Washington. The author has contributed to research in topics: Mass spectrometry & Proteome. The author has an hindex of 77, co-authored 168 publications receiving 35701 citations. Previous affiliations of Jimmy K. Eng include Oregon Health & Science University & Fred Hutchinson Cancer Research Center.
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The Application of New Software Tools to Quantitative Protein Profiling Via Isotope-coded Affinity Tag (ICAT) and Tandem Mass Spectrometry II. Evaluation of Tandem Mass Spectrometry Methodologies for Large-Scale Protein Analysis, and the Application of Statistical Tools for Data Analysis and Interpretation
Priska D. von Haller,Eugene C. Yi,Samuel Donohoe,Kelly Vaughn,Andrew Keller,Alexey I. Nesvizhskii,Jimmy K. Eng,Xiao jun Li,David R. Goodlett,Ruedi Aebersold,Julian D. Watts +10 more
TL;DR: The isotope-coded affinity tag (ICAT) approach to quantitative protein profiling, in this case proteins that copurified with lipid raft plasma membrane domains isolated from control and stimulated Jurkat human T cells, was applied and the accuracy of peptide and protein identifications made was estimated.
Journal ArticleDOI
UniPep - a database for human N -linked glycosites: a resource for biomarker discovery
Hui Zhang,Paul Loriaux,Jimmy K. Eng,David S. Campbell,Andy Keller,Pat Moss,Richard Bonneau,Ning Zhang,Yong Zhou,Bernd Wollscheid,Kelly Cooke,Eugene C. Yi,Hookeun Lee,Elaine R. Peskind,Jing Zhang,Richard D. Smith,Reudi Aebersold +16 more
TL;DR: UniPep as discussed by the authors is a database of human N-linked glycosites for biomarker discovery, which represents the proteomes of plasma, the cell surface and secreted proteins at very low redundancy and provides a compelling link between the tissue and plasma proteomes.
Journal ArticleDOI
Protein Interactions, Post-translational Modifications and Topologies in Human Cells
TL;DR: The results presented here provide new details on the structures of known multi-protein complexes as well as evidence for new protein-protein interactions.
Journal ArticleDOI
Proteomics of rat liver Golgi complex: minor proteins are identified through sequential fractionation.
TL;DR: The data suggest that cell fractionation followed by biochemical dissection of specific classes of molecules provides a significant advantage for the identification of low abundance proteins in organelles.