| Literature DB >> 26947772 |
Joseph Markowitz1,2, Tapas K Mal3, Chunhua Yuan3, Nicholas B Courtney2, Mitra Patel2, Andrew R Stiff2, James Blachly2, Christopher Walker2, Ann-Kathrin Eisfeld2, Albert de la Chapelle2, William E Carson2,4.
Abstract
It was recently discovered that the NRAS isoform 5 (20 amino acids) is expressed in melanoma and results in a more aggressive cell phenotype. This novel isoform is responsible for increased phosphorylation of downstream targets such as AKT, MEK, and ERK as well as increased cellular proliferation. This structure report describes the NMR solution structure of NRAS isoform 5 to be used as a starting point to understand its biophysical interactions. The isoform is highly flexible in aqueous solution, but forms a helix-turn-coil structure in the presence of trifluoroethanol as determined by NMR and CD spectroscopy.Entities:
Keywords: NMR; NRAS; isoform; melanoma
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Year: 2016 PMID: 26947772 PMCID: PMC4838646 DOI: 10.1002/pro.2916
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725