As part of its intracellular cycle, the first interaction of the parasite with the target cell is performed with the surface proteins known as the SRS superfamily (Surface Antigen Glycoprotein – Related Sequences).
In this modular organization the first interaction of a vesicle and its target membrane is termed tethering.
First, interaction of a virus glycoprotein with its receptor may convert the glycoprotein from its native state to a new metastable state resulting in a long-lived envelope protein-receptor intermediate.
Within the interactome of S. cerevisiae, the first interaction of a given protein increases its rate of gaining a new one by approximately 100%.
For example, the first interaction of Table 4 shows the switching mechanism of two genes, COX6C and UBA1, being controlled by a SNP in LARP4.
First, interaction of fear appeal dynamics with SOB caused the outcomes of meta-analyses so far to be biased; and second, in the case of threatening information, intention is not a reliable outcome measure.
For example, for COX6C and UBA1, the gene pair of the first interaction of Table 4, we found a switching mechanism in GDS2960_1 with the P-value of −3.9532, showing the statistical significance of this mechanism.
The first interaction of a phage particle and a bacterium is mediated through the specific recognition between the phage receptor binding protein (RBP), located at the tip of the tail, and the host cell receptor distributed over the cell surface.
First, interaction of a positively charged WLM domain with DNA may induce conformational changes facilitating displacement from the active site of the negatively charged C-terminal peptide bearing the inhibitory cysteine.
