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On the other hand, the channel can be further categorized on the basis of time selectivity conditions.
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Consequently, the time selectivity of the channel would be decreased as the frequency selectivity increasing.
This series was evaluated on the basis of potency, selectivity, and rat pharmacokinetic parameters.
The molecular basis of this selectivity remains unknown.
To examine the structural basis of this selectivity, we compared the sequences and structures of these two proteins.
Based on our observations, we suggest that conserved residues along with residue variations at conserved positions form the basis of TR selectivity and specificity.
The structural basis of VRAC selectivity is currently unknown.
The NIPs have been divided into three groups on the basis of their selectivity filter structure.
Using molecular modelling and biochemical studies, we explain the basis of this selectivity.
The molecular basis of substrate selectivity in AHL synthases, however, remains poorly understood.
Further analysis of the critical targets of the oncogenic ETS factors is needed to reveal the basis of this selectivity.
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