2VWF

Grb2 SH3C (2)

Summary for 2VWF

• Entry DOI: 10.2210/pdb2vwf/pdb
• Related: 1AZE 1BM2 1BMB 1CJ1 1FHS 1FYR 1GCQ 1GFC 1GFD 1GHU 1GRI 1IO6 1JYQ 1JYR 1JYU 1QG1 1TZE 1X0N 1ZFP 2AOA 2AOB 2H46 2VVK
• Descriptor: GROWTH FACTOR RECEPTOR-BOUND PROTEIN 2, GRB2-ASSOCIATED-BINDING PROTEIN 2 (3 entities in total)
• Functional Keywords: polymorphism, phosphoprotein, golgi apparatus, grb2, alternative splicing, host-virus interaction, sh3c, signaling, sh2 domain, sh3 domain, protein-binding, protein binding
• Biological source: HOMO SAPIENS (HUMAN); More
• Cellular location: Golgi apparatus (By similarity): P62993; Cytoplasm: Q9UQC2
• Total number of polymer chains: 2
• Total formula weight: 8388.32

Authors

Harkiolaki, M.,Tsirka, T.,Feller, S.M. (deposition date: 2008-06-24, release date: 2009-05-19, Last modification date: 2023-12-13)

Primary citation

Harkiolaki, M.,Tsirka, T.,Lewitzky, M.,Simister, P.C.,Joshi, D.,Bird, L.E.,Jones, E.Y.,O'Reilly, N.,Feller, S.M.
Distinct Binding Modes of Two Epitopes in Gab2 that Interact with the Sh3C Domain of Grb2.
Structure, 17:809-, 2009

PubMed Abstract: Grb2 and Gab2 form a complex implicated in normal cell signaling and cancer development. Binding of the Grb2SH3C domain to Gab2 is essential for the interaction, but molecular details remained undefined. Using peptide arrays and isothermal titration calorimetry, two Grb2SH3C binding sites in Gab2 (Gab2a and Gab2b) were confirmed and characterized. Gab2a bears similarity to a p27Kip1 epitope that also binds Grb2SH3C. Crystal structures of both Gab2 epitopes complexed with Grb2SH3C reveal that Gab2b contains a 3(10) helix that positions the arginine and lysine of the core-binding motif RxxK in parallel orientation. In contrast, the Gab2a RxxK motif is embedded in a PPII helix with Arg and Lys in staggered orientation. A similar interaction mode is also present in a new complex of Mona/GadsSH3C with an RxxxxK epitope from the putative phosphatase HD-PTP. In summary, our study reveals interaction types of SH3 domains, highlighting their great versatility.

PubMed: 19523899
DOI: 10.1016/J.STR.2009.03.017

Experimental method

X-RAY DIFFRACTION (1.58 Å)