Literature DB >> 14744431

Specificity in signal transduction: from phosphotyrosine-SH2 domain interactions to complex cellular systems.

Tony Pawson1.   

Abstract

Over the last two decades, a new and unifying concept of cellular organization has emerged in which modular protein-protein interactions provide an underlying framework through which signaling pathways are assembled and controlled. In this scheme, posttranslational modifications such as phosphorylation commonly exert their biological effects by regulating molecular interactions, exemplified by the ability of phosphotyrosine sites to bind selectively to SH2 domains. Although these interactions are rather simple in isolation, they can nonetheless be exploited to generate complex cellular systems. Here, I discuss experiments that have led to this view of dynamic cellular behavior and identify some current and future areas of interest in cell signaling.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14744431     DOI: 10.1016/s0092-8674(03)01077-8

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  266 in total

1.  Tyrosine residues at the carboxyl terminus of Vav1 play an important role in regulation of its biological activity.

Authors:  Galit Lazer; Liron Pe'er; Marganit Farago; Kazuya Machida; Bruce J Mayer; Shulamit Katzav
Journal:  J Biol Chem       Date:  2010-05-10       Impact factor: 5.157

2.  RACK1 regulates G1/S progression by suppressing Src kinase activity.

Authors:  Vidya Mamidipudi; Jian Zhang; Kelly C Lee; Christine A Cartwright
Journal:  Mol Cell Biol       Date:  2004-08       Impact factor: 4.272

3.  Purification, crystallization and preliminary X-ray diffraction analysis of the Fyn SH2 domain and its complex with a phosphotyrosine peptide.

Authors:  Radu Huculeci; Lieven Buts; Tom Lenaerts; Nico A J van Nuland; Abel Garcia-Pino
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-02-29

4.  Data-driven modelling of receptor tyrosine kinase signalling networks quantifies receptor-specific potencies of PI3K- and Ras-dependent ERK activation.

Authors:  Murat Cirit; Jason M Haugh
Journal:  Biochem J       Date:  2012-01-01       Impact factor: 3.857

Review 5.  Quantitative phosphoproteomics: New technologies and applications in the DNA damage response.

Authors:  Huilin Zhou; Claudio P Albuquerque; Jason Liang; Raymond T Suhandynata; Stephanie Weng
Journal:  Cell Cycle       Date:  2010-09-26       Impact factor: 4.534

6.  A combination of multisite phosphorylation and substrate sequestration produces switchlike responses.

Authors:  Xinfeng Liu; Lee Bardwell; Qing Nie
Journal:  Biophys J       Date:  2010-04-21       Impact factor: 4.033

7.  Loops govern SH2 domain specificity by controlling access to binding pockets.

Authors:  Tomonori Kaneko; Haiming Huang; Bing Zhao; Lei Li; Huadong Liu; Courtney K Voss; Chenggang Wu; Martin R Schiller; Shawn Shun-Cheng Li
Journal:  Sci Signal       Date:  2010-05-04       Impact factor: 8.192

8.  The structural and energetic basis for high selectivity in a high-affinity protein-protein interaction.

Authors:  Nicola A G Meenan; Amit Sharma; Sarel J Fleishman; Colin J Macdonald; Bertrand Morel; Ruth Boetzel; Geoffrey R Moore; David Baker; Colin Kleanthous
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-17       Impact factor: 11.205

Review 9.  Current status of molecularly targeted therapy for hepatocellular carcinoma: basic science.

Authors:  Shinji Tanaka; Shigeki Arii
Journal:  Int J Clin Oncol       Date:  2010-05-27       Impact factor: 3.402

10.  Src binds cortactin through an SH2 domain cystine-mediated linkage.

Authors:  Jason V Evans; Amanda G Ammer; John E Jett; Chris A Bolcato; Jason C Breaux; Karen H Martin; Mark V Culp; Peter M Gannett; Scott A Weed
Journal:  J Cell Sci       Date:  2012-10-24       Impact factor: 5.285

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.