Literature DB >> 15668520

Protein-protein interactions in the regulation of the extracellular signal-regulated kinase.

Dana Chuderland1, Rony Seger.   

Abstract

The extracellular signal-regulated kinase (ERK) cascade is a central intracellular signaling pathway that is activated by a variety of extracellular stimuli, and thereby regulates cellular processes such as proliferation, differentiation, and oncogenic transformation. To execute these functions, the signals of those stimuli are transmitted to the cytosolic and nuclear targets in a rapid and specific manner. In the last few years it has become clear that the specificity and the rapid function of the ERK cascade is largely determined by protein-protein interactions with various signaling components and substrates. This review describes interactions of ERK with its immediate regulators, scaffold proteins, substrates, and localizing proteins, and shows their involvement in the functioning of the ERK cascade. Understanding the full scope of ERK-interactions is important for the development of new drugs for the treatment of cancer and other diseases.

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Year:  2005        PMID: 15668520     DOI: 10.1385/MB:29:1:57

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  154 in total

1.  Rewiring MAP kinase pathways using alternative scaffold assembly mechanisms.

Authors:  Sang-Hyun Park; Ali Zarrinpar; Wendell A Lim
Journal:  Science       Date:  2003-01-02       Impact factor: 47.728

2.  The proliferative and antiapoptotic effects of substance P are facilitated by formation of a beta -arrestin-dependent scaffolding complex.

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Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

3.  Coupling of the RAS-MAPK pathway to gene activation by RSK2, a growth factor-regulated CREB kinase.

Authors:  J Xing; D D Ginty; M E Greenberg
Journal:  Science       Date:  1996-08-16       Impact factor: 47.728

4.  Multiple regions of MAP kinase phosphatase 3 are involved in its recognition and activation by ERK2.

Authors:  B Zhou; L Wu; K Shen; J Zhang; D S Lawrence; Z Y Zhang
Journal:  J Biol Chem       Date:  2000-12-04       Impact factor: 5.157

5.  Extracellular regulated kinase (ERK) interaction with actin and the calponin homology (CH) domain of actin-binding proteins.

Authors:  B D Leinweber; P C Leavis; Z Grabarek; C L Wang; K G Morgan
Journal:  Biochem J       Date:  1999-11-15       Impact factor: 3.857

Review 6.  New mechanisms in heptahelical receptor signaling to mitogen activated protein kinase cascades.

Authors:  K L Pierce; L M Luttrell; R J Lefkowitz
Journal:  Oncogene       Date:  2001-03-26       Impact factor: 9.867

7.  Isolation and characterization of two growth factor-stimulated protein kinases that phosphorylate the epidermal growth factor receptor at threonine 669.

Authors:  I C Northwood; F A Gonzalez; M Wartmann; D L Raden; R J Davis
Journal:  J Biol Chem       Date:  1991-08-15       Impact factor: 5.157

8.  A reinvestigation of the multisite phosphorylation of the transcription factor c-Jun.

Authors:  Simon Morton; Roger J Davis; Ann McLaren; Philip Cohen
Journal:  EMBO J       Date:  2003-08-01       Impact factor: 11.598

Review 9.  Specificity of receptor tyrosine kinase signaling: transient versus sustained extracellular signal-regulated kinase activation.

Authors:  C J Marshall
Journal:  Cell       Date:  1995-01-27       Impact factor: 41.582

10.  A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells.

Authors:  J Han; J D Lee; L Bibbs; R J Ulevitch
Journal:  Science       Date:  1994-08-05       Impact factor: 47.728

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  45 in total

1.  ERK1 and ERK2 regulate embryonic stem cell self-renewal through phosphorylation of Klf4.

Authors:  Myoung Ok Kim; Sung-Hyun Kim; Yong-Yeon Cho; Janos Nadas; Chul-Ho Jeong; Ke Yao; Dong Joon Kim; Dong-Hoon Yu; Young-Sam Keum; Kun-Yeong Lee; Zunnan Huang; Ann M Bode; Zigang Dong
Journal:  Nat Struct Mol Biol       Date:  2012-02-05       Impact factor: 15.369

2.  Tyrosine phosphorylation of CD13 regulates inflammatory cell-cell adhesion and monocyte trafficking.

Authors:  Jaganathan Subramani; Mallika Ghosh; M Mamunur Rahman; Leslie A Caromile; Claire Gerber; Karim Rezaul; David K Han; Linda H Shapiro
Journal:  J Immunol       Date:  2013-08-30       Impact factor: 5.422

Review 3.  The ERK cascade: a prototype of MAPK signaling.

Authors:  Hadara Rubinfeld; Rony Seger
Journal:  Mol Biotechnol       Date:  2005-10       Impact factor: 2.695

4.  Quantitative analysis of ERK2 interactions with substrate proteins: roles for kinase docking domains and activity in determining binding affinity.

Authors:  Kimberly A Burkhard; Fengming Chen; Paul Shapiro
Journal:  J Biol Chem       Date:  2010-11-22       Impact factor: 5.157

Review 5.  How do pleiotropic kinase hubs mediate specific signaling by TNFR superfamily members?

Authors:  Bärbel Schröfelbauer; Alexander Hoffmann
Journal:  Immunol Rev       Date:  2011-11       Impact factor: 12.988

6.  Nuclear extracellular signal-regulated kinase 1 and 2 translocation is mediated by casein kinase 2 and accelerated by autophosphorylation.

Authors:  Alexander Plotnikov; Dana Chuderland; Yael Karamansha; Oded Livnah; Rony Seger
Journal:  Mol Cell Biol       Date:  2011-07-05       Impact factor: 4.272

7.  Mechanisms of MPP⁺-induced PC12 cell apoptosis via reactive oxygen species.

Authors:  Qing Zhu; Jing Wang; Yunjian Zhang; Shenggang Sun
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2012-12-28

8.  mCSM-PPI2: predicting the effects of mutations on protein-protein interactions.

Authors:  Carlos H M Rodrigues; Yoochan Myung; Douglas E V Pires; David B Ascher
Journal:  Nucleic Acids Res       Date:  2019-07-02       Impact factor: 16.971

9.  Activation of the extracellular signal regulated kinase (ERK) pathway in human melanoma.

Authors:  L Zhuang; C S Lee; R A Scolyer; S W McCarthy; A A Palmer; X D Zhang; J F Thompson; L P Bron; P Hersey
Journal:  J Clin Pathol       Date:  2005-11       Impact factor: 3.411

10.  A preformed signaling complex mediates GnRH-activated ERK phosphorylation of paxillin and FAK at focal adhesions in L beta T2 gonadotrope cells.

Authors:  Masha Dobkin-Bekman; Michal Naidich; Liat Rahamim; Fiorenza Przedecki; Tal Almog; Stefan Lim; Philippa Melamed; Ping Liu; Thorsten Wohland; Zhong Yao; Rony Seger; Zvi Naor
Journal:  Mol Endocrinol       Date:  2009-07-23
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