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An experimentally derived database of candidate Ras-interacting proteins.
Goldfinger, Lawrence E; Ptak, Celeste; Jeffery, Erin D; Shabanowitz, Jeffrey; Han, Jaewon; Haling, Jacob R; Sherman, Nicholas E; Fox, Jay W; Hunt, Donald F; Ginsberg, Mark H.
Affiliation
  • Goldfinger LE; Division of Rheumatology, Department of Medicine, University of California, San Diego, La Jolla, California 92093, USA. lgoldfinger@ucsd.edu
J Proteome Res ; 6(5): 1806-11, 2007 May.
Article in En | MEDLINE | ID: mdl-17439166
ABSTRACT
We used a TAP-tag approach to identify candidate binding proteins for the related Ras family GTPases H-Ras, R-Ras, and Rap1A. Protein complexes were isolated from mouse fibroblasts, and component proteins were identified by a combination of nanoflow HPLC and tandem mass spectrometry. H-Ras was found to associate with numerous cytoskeletal proteins including talin-1. R-Ras and Rap1A each associated with various signaling molecules, many of which are membrane-associated. Thus, we have established the first database of potential Ras interactors in mammalian cells.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, Affinity / Ras Proteins / Rap1 GTP-Binding Proteins / Databases, Protein Limits: Animals Language: En Journal: J Proteome Res Journal subject: BIOQUIMICA Year: 2007 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, Affinity / Ras Proteins / Rap1 GTP-Binding Proteins / Databases, Protein Limits: Animals Language: En Journal: J Proteome Res Journal subject: BIOQUIMICA Year: 2007 Document type: Article Affiliation country: