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Structural analysis in a membrane revealed that all extracellular loops of rhomboid make stabilizing interactions with substrate, but mainly through backbone interactions, explaining rhomboid's broad sequence selectivity.
From each analysis, the number of markers and their interactions explaining the variation in gene expression was determined and used in further analysis.
Here, we were able to report specific examples of interactions explaining noticeable fractions of variation in human gene expression, with in many cases the interaction contributing more than the marginal effects to overall variance.
The presence of additional +2 subsite interactions (explaining the more beneficial turnover of xylotriose in WXyn43 compared with the L. brevis enzymes) is unclear, but may in WXyn43 include interaction with a loop (Val505 Gly510).
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These interactions explain the spherical growth and inhibition in some planes.
Here, even the simple LM method performs nearly optimal due to the simplified higher-layer interactions explained in Section 4.2.
The chemical and structural complexity of enzymes, as well as their interactions, explains why an enzyme's activity can be affected in both subtle and substantial ways.
"Explained perturbed interactions" indicates the number of perturbed interactions explained by the links in the BPLN.
Predicted domain-domain interactions explain all interactions in about 25% of such complexes.
Five additive x dominant interactions explained on average 0.79% (maximum 1.33%) and four dominant x additive interactions explained 0.24% (maximum 0.67%).
Figure 4 shows the dense network of interactions explained by this link.
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CEO of Professional Science Editing for Scientists @ prosciediting.com