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In contrast to this functional divergence, convergence of function is also seen in the superfamily, specifically concerning binding of tRNA, and structural mimics of tRNA.
Therefore, under the hypothesis that there is an underlying dynamics (i.e., fluctuation profile) for the three-dimensional (3-D) structure of a protein, which is crucial for the function, our metric dfi quantifies the contribution of each position to this functional dynamics and is designed to capture the key residues mediating the function through the residue interaction dynamics.
For results related to this functional, see [28, 29].
Moreover, the observed increased expression of tyrosine hydroxylase by cells transplanted with PAMs may contribute to this functional recovery.
Although central architectures that support robust oscillations have been extensively studied, networks containing the same core vary drastically in their potential to oscillate, and it remains elusive what peripheral modifications to the core contribute to this functional variation.
Linked to this, functional strategies are needed for community participation in decision-making processes that are not limited to post-disaster phases but implemented in day-to-day politics, as argued for the case of Sri Lanka (Khazai et al. 2006).
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It is difficult to see this functional coalition extending to other areas.
Systemic typology essentially belongs to this functional-typological tradition (see further below for details).
To achieve this, functional models relating customer preferences to engineering characteristics need to be developed.
To separate this functional phenomenon from a particular mechanism, we refer to it as specific immune priming.
A two-step procedure was used to prepare this functional porous structure.
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