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DPI states that, if X i interacts with X j through a random variable X k then I(X i, X j ) < min{ I(X i, X k ), I X j, X k )}.
In the Snf7 protofilament, the protomer (i) interacts with the next protomer (i+1) through both hydrophobic and electrostatic interactions, burying ~1060 Å of solvent-accessible surface area per protomer.
In this example, the atom i interacts with eight solvent atoms and five the other solute atoms.
The experience of the social world by the "I" thereby justifies and corroborates itself (as a being-in-the-world) through the experience of the others with whom the "I" interacts.
We construct a drug-target relationship matrix A whose element A i,j) is 1 if drug i interacts with target j, otherwise 0. The matrix is sparse; the total number of connections among the drugs and targets is only 2,557, with 687 drugs having at least one known target and with 628 proteins having at least one drug.
The oscillator at node i interacts with the network via an effective coupling strength = Kk i r i. CLRP is used to compare two weighted networks.
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For drug d i interacting with T i targets, t p i and t q i ~ denote the target interacting and not interacting with d i, respectively.
Because apoA-I interacts through protein PL and protein protein interactions at the HDL particle surface, it is likely that the many minor protein constituents of HDL detected by proteomics analysis also interact similarly and become transported in plasma as part of HDL.
These results confirm that RIG-I interacts only with RNAs that are agonists for signal transduction.
This suggests that the RIG-I interacts with dsR27 but not with cssR27.
RIG-I interacts with its ligands by means of its central ATP-binding helicase domain as well as its carboxyterminal regulatory domain (RD; see the schematic representation in Fig. 1A).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com