Literature DB >> 20946842

Kinetic studies of the yeast His-Asp phosphorelay signaling pathway.

Alla O Kaserer1, Babak Andi, Paul F Cook, Ann H West.   

Abstract

For both prokaryotic and eukaryotic His-Asp phosphorelay signaling pathways, the rates of protein phosphorylation and dephosphorylation determine the stimulus-to-response time frame. Thus, kinetic studies of phosphoryl group transfer between signaling partners are important for gaining a full understanding of how the system is regulated. In many cases, the phosphotransfer reactions are too fast for rates to be determined by manual experimentation. Rapid quench flow techniques thus provide a powerful method for studying rapid reactions that occur in the millisecond time frame. In this chapter, we describe experimental design and procedures for kinetic characterization of the yeast SLN1-YPD1-SSK1 osmoregulatory phosphorelay system using a rapid quench flow kinetic instrument.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20946842      PMCID: PMC2957298          DOI: 10.1016/S0076-6879(10)71004-1

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  29 in total

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Journal:  Methods Enzymol       Date:  2010-03-01       Impact factor: 1.600

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Authors:  Jade Mei-Yeh Lu; Robert J Deschenes; Jan S Fassler
Journal:  Eukaryot Cell       Date:  2003-12

4.  Effects of osmolytes on the SLN1-YPD1-SSK1 phosphorelay system from Saccharomyces cerevisiae.

Authors:  Alla O Kaserer; Babak Andi; Paul F Cook; Ann H West
Journal:  Biochemistry       Date:  2009-08-25       Impact factor: 3.162

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Authors:  J L Brown; S North; H Bussey
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6.  Crystal structure of a complex between the phosphorelay protein YPD1 and the response regulator domain of SLN1 bound to a phosphoryl analog.

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10.  Yeast Skn7p functions in a eukaryotic two-component regulatory pathway.

Authors:  J L Brown; H Bussey; R C Stewart
Journal:  EMBO J       Date:  1994-11-01       Impact factor: 11.598

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4.  Structural insights into the histidine-containing phospho-transfer protein and receiver domain of sensor histidine kinase suggest a complex model in the two-component regulatory system in Pseudomonas aeruginosa.

Authors:  Shao-Kang Chen; Hong-Hsiang Guan; Pei-Hsun Wu; Li-Ting Lin; Meng-Chun Wu; Hwan-You Chang; Nai-Chi Chen; Chien-Chih Lin; Phimonphan Chuankhayan; Yen-Chieh Huang; Pei-Ju Lin; Chun-Jung Chen
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  4 in total

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