Literature DB >> 26420231

The discovery of modular binding domains: building blocks of cell signalling.

Bruce J Mayer1.   

Abstract

Cell signalling - the ability of a cell to process information from the environment and change its behaviour in response - is a central property of life. Signalling depends on proteins that are assembled from a toolkit of modular domains, each of which confers a specific activity or function. The discovery of modular protein- and lipid-binding domains was a crucial turning point in understanding the logic and evolution of signalling mechanisms.

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Year:  2015        PMID: 26420231     DOI: 10.1038/nrm4068

Source DB:  PubMed          Journal:  Nat Rev Mol Cell Biol        ISSN: 1471-0072            Impact factor:   94.444


  94 in total

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Review 3.  Reading protein modifications with interaction domains.

Authors:  Bruce T Seet; Ivan Dikic; Ming-Ming Zhou; Tony Pawson
Journal:  Nat Rev Mol Cell Biol       Date:  2006-07       Impact factor: 94.444

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Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-15       Impact factor: 11.205

5.  Crystal structure of the Src family tyrosine kinase Hck.

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Journal:  Nature       Date:  1997-02-13       Impact factor: 49.962

Review 6.  Signals past, present, and future.

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Journal:  Cell       Date:  1985-04       Impact factor: 41.582

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Journal:  Cell       Date:  1996-03-22       Impact factor: 41.582

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Authors:  D Anderson; C A Koch; L Grey; C Ellis; M F Moran; T Pawson
Journal:  Science       Date:  1990-11-16       Impact factor: 47.728

10.  Comparative analysis of Saccharomyces cerevisiae WW domains and their interacting proteins.

Authors:  Jay R Hesselberth; John P Miller; Anna Golob; Jason E Stajich; Gregory A Michaud; Stanley Fields
Journal:  Genome Biol       Date:  2006-04-10       Impact factor: 13.583

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2.  DLC2 inhibits development of glioma through regulating the expression ratio of TAp73α/TAp73β.

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Journal:  Biology (Basel)       Date:  2017-12-06

4.  MC159 of Molluscum Contagiosum Virus Suppresses Autophagy by Recruiting Cellular SH3BP4 via an SH3 Domain-Mediated Interaction.

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5.  Direct Phosphorylation of SRC Homology 3 Domains by Tyrosine Kinase Receptors Disassembles Ligand-Induced Signaling Networks.

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6.  SOS1 interacts with Grb2 through regions that induce closed nSH3 conformations.

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7.  Bitopic Inhibition of ATP and Substrate Binding in Ser/Thr Kinases through a Conserved Allosteric Mechanism.

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Review 10.  Novel Roles of SH2 and SH3 Domains in Lipid Binding.

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