Literature DB >> 14501138

Preliminary structure analysis of the DH/PH domains of leukemia-associated RhoGEF.

Romana Kristelly1, Brett T Earnest, Lakshmipriya Krishnamoorthy, John J G Tesmer.   

Abstract

Leukemia-associated RhoGEF (LARG) is a multidomain protein that relays signals from Galpha(12/13)-coupled heptahelical receptors to GTPases that regulate the cytoskeleton. To understand the molecular basis of LARG-mediated signal transduction, structural analysis of its DH/PH domains has been initiated. The LARG DH/PH domains have been overexpressed in Escherichia coli as a TEV protease-cleavable fusion protein containing maltose-binding protein and a hexahistidine tag at the N- and C-termini, respectively. Crystals of the DH/PH domains were obtained (space group C2; unit-cell parameters a = 195.5, b = 46.0, c = 75.1 A, beta = 105.0 degrees ) and xenon and NaBr derivatives were generated which should allow the structure to be determined by MIRAS.

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Year:  2003        PMID: 14501138     DOI: 10.1107/s0907444903018067

Source DB:  PubMed          Journal:  Acta Crystallogr D Biol Crystallogr        ISSN: 0907-4449


  14 in total

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10.  High-throughput screening for small-molecule inhibitors of LARG-stimulated RhoA nucleotide binding via a novel fluorescence polarization assay.

Authors:  Chris R Evelyn; Timothy Ferng; Rafael J Rojas; Martha J Larsen; John Sondek; Richard R Neubig
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