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Probing the ligand binding domain of the GluR2 receptor by proteolysis and deletion mutagenesis defines domain boundaries and yields a crystallizable construct.
Chen GQ, Sun Y, Jin R, Gouaux E. Chen GQ, et al. Among authors: gouaux e. Protein Sci. 1998 Dec;7(12):2623-30. doi: 10.1002/pro.5560071216. Protein Sci. 1998. PMID: 9865957 Free PMC article.
To identify the proteolytic fragments, Maldi mass spectrometry and N-terminal amino acid sequencing were employed. Trypsin digestion of HS1S2 (Chen GQ, Gouaux E. 1997. Proc Natl Acad Sci USA 94:13431-13436) in the presence and absence of glutamate showed that the li …
To identify the proteolytic fragments, Maldi mass spectrometry and N-terminal amino acid sequencing were employed. Trypsin digestion of HS1S …
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