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Data is also provided to analyze the effect of wave current interaction on structural loads.
Quantifying the impact of this interaction on structural vulnerability is critical for risk assessment and informed decision-making.
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Taken together, the E. cuniculi Mot1NTD TBP DNA NC2 crystal structure shows a high degree of evolutionary conservation of the TBP NC2 interaction on a structural level.
PRISM predicts protein interactions based on structural and evolutionary similarity to known protein interfaces.
Since then, the use of automatic learning methods to assign putative functions to genes, based not only on their expression profiles but also on protein protein interactions and on structural similarities, has led to a broad diversity of strategies and to a profuse bibliography [ 16– 20, 58].
Here, we introduce an implementation of interaction profiles [1] based on Structural Interaction Fingerprints (SIFt) [2], which allow precise and rapid binding site description.
The predictions for the examples MicA- ompA, OxyS- fhlA, RyhB- sodB and RyhB- uof-fur were compared with the interaction models based on structural mapping as described by Argaman and Altuvia (2000); Geissmann and Touati (2004); Udekwu et al. (2005) and Večerek et al. (2007).
The role of the long-ranged Coulombic interactions on the structural features and chain dynamics of the polymer were also examined.
Chemo-mechanical interactions on the structural level are investigated in the numerical simulation of a concrete beam subjected simultaneously to mechanical loads and deionized water.
While the biological actions of IGF-1-IGFBP-IGF-1R axis have been extensively studied, a complete understanding of IGF-IGFBP interactions on a structural level is lacking.
Protein domain information was extracted from InterPRO (drug-protein interactions are based on structural properties) [48].
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