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Grb2 - Wikipedia, the free encyclopedia

Grb2

From Wikipedia, the free encyclopedia

Grb2 is an adaptor protein involved in signal transduction/cell communication. The name Grb2 is an abbreviation of Growth factor receptor-bound protein 2.

Growth factor receptor-bound protein 2
PDB rendering based on 1aze.
Available structures: 1aze, 1bm2, 1bmb, 1cj1, 1fhs, 1fyr, 1gbq, 1gbr, 1gcq, 1gfc, 1gfd, 1ghu, 1gri, 1io6, 1jyq, 1jyr, 1jyu, 1qg1, 1tze, 1x0n, 1zfp, 2aoa, 2aob, 2gbq, 2h46, 2h5k, 2huw, 2huy, 3gbq, 4gbq
Identifiers
Symbol(s) GRB2; ASH; EGFRBP-GRB2; Grb3-3; MST084; MSTP084
External IDs OMIM: 108355 MGI95805 HomoloGene1576
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 2885 14784
Ensembl ENSG00000177885 ENSMUSG00000059923
Uniprot P62993 Q3U1Q4
Refseq NM_002086 (mRNA)
NP_002077 (protein)
NM_008163 (mRNA)
NP_032189 (protein)
Location Chr 17: 70.83 - 70.91 Mb Chr 11: 115.46 - 115.52 Mb
Pubmed search [1] [2]

The protein encoded by this gene binds the epidermal growth factor receptor and contains one SH2 domain and two SH3 domains. Its two SH3 domains direct complex formation with proline-rich regions of other proteins, and its SH2 domain binds tyrosine phosphorylated sequences. This gene is similar to the Sem5 gene of Caenorhabditis elegans, which is involved in the signal transduction pathway. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene.[1]

Contents

[edit] Function and expression

Grb2 is widely expressed and is essential for multiple cellular functions. Inhibition of Grb2 function impairs developmental processes in various organisms and blocks transformation and proliferation of various cell types, and so it is not surprising that a targeted gene disruption of Grb2 in mouse is lethal at an early embryonic stage. Grb2 is best known for its ability to link the epidermal growth factor receptor tyrosine kinase to the activation of Ras and its downstream kinases, ERK1,2. Grb2 is composed of an SH2 domain flanked on each side by an SH3 domain. Grb2 has two closely related proteins with similar domain organizations, Gads and Grap. Gads and Grap are expressed specifically in hematopoietic cells and function in the coordination of tyrosine kinase mediated signal transduction.

[edit] Domains

The SH2 domain of Grb2 binds to phosphorylated tyrosine containing peptides on receptors or scaffold proteins with a preference for pY-X-N-X, where X is generally a hydrophobic residue such as valine (see The SH2 Website).

The N-terminal SH3 domain binds to proline-rich peptide peptides and can bind to the Ras-guanine exchange factor SOS.

The C-terminal SH3 domain binds to peptides conforming to a P-X-I/L/V/-D/N-R-X-X-K-P motif that allows it to specifically bind to proteins such as Gab-1.[2]

[edit] References

  1. ^ Entrez Gene: GRB2 growth factor receptor-bound protein 2.
  2. ^ Berry DM, Nash P, Liu SK, Pawson T, McGlade CJ (2002). "A high-affinity Arg-X-X-Lys SH3 binding motif confers specificity for the interaction between Gads and SLP-76 in T cell signaling". Curr. Biol. 12 (15): 1336–41. PMID 12176364. 

[edit] Further reading

  • Colledge M, Froehner SC (1998). "Interaction between the nicotinic acetylcholine receptor and Grb2. Implications for signaling at the neuromuscular junction.". Ann. N. Y. Acad. Sci. 841: 17–27. PMID 9668219. 
  • Ramesh N, Antón IM, Martínez-Quiles N, Geha RS (1999). "Waltzing with WASP.". Trends Cell Biol. 9 (1): 15–9. PMID 10087612. 
  • O'Sullivan E, Kinnon C, Brickell P (1999). "Wiskott-Aldrich syndrome protein, WASP.". Int. J. Biochem. Cell Biol. 31 (3-4): 383–7. PMID 10224664. 
  • Schlaepfer DD, Hauck CR, Sieg DJ (1999). "Signaling through focal adhesion kinase.". Prog. Biophys. Mol. Biol. 71 (3-4): 435–78. PMID 10354709. 
  • Vidal M, Liu WQ, Gril B, et al. (2004). "[Design of new anti-tumor agents interrupting deregulated signaling pathways induced by tyrosine kinase proteins. Inhibition of protein-protein interaction involving Grb2]". J. Soc. Biol. 198 (2): 133–7. PMID 15368963. 


[edit] External links

[edit] External links

[edit] See also


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