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Effects of glycosylation on peptide conformation: a synergistic experimental and computational study
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All sequence-specific effects are restricted to a single local length scale, denoted as l^sub s^
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Lower concentration rates of protein to trypsin were used (100:1, 200:1, and 300:1), but in all these experiments the amount of nondigested EI^sup sc^ in the absence of effectors was insignificant after 1 min of reaction (data not shown)
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Taken together, these data suggest that there were structural changes, which partially solvent-exposed the indole moiety and/or tyrosine residues, and modified the ellipticity at 222 nm (41,42)
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Binding of the catabolite repressor protein to its DNA target is regulated by phopshorylation of its co-represser HPr
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Time-resolved fluorescenceTime-resolved measurements of tryptophan (Trp) fluorescence were recorded using an IBH (Glasgow, UK) 5000 U fluorescence lifetime spectrometer system with 1 nm resolved excitation and emission monochromators (5000 M)
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The proportions decreased front 0
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, Uppsala, Swedent as follows: 3 mL of monoclonal antibodies solution (hybridoma supernatant solution) obtained in this study was added to 0
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The loss of phenotypic traits by differentiated cells in vitro
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