One of the common strategies to define a reference clustering for a set of molecular structures requires the involvement of expert knowledge.
While a calculation of the molecular structure is required to fully ascertain the possibility of PAI in each system, we expect that it occurs to varying degrees in, at least, Yb, Tm, Dy, Sr, and Ba MOTs.
The assembly of the SpaDEF precursors into a high-molecular-weight pilus structure requires the pilus-specific sortases SrtB and SrtC that are encoded within the spaDEF gene region of C. diphtheriae [ 55].
However, a mechanistic understanding of how individual molecular components work together in a system requires knowledge of molecular structures, and their interactions.
A mechanistic understanding of how individual molecular components work together in a system, and how the system is affected and adapted to individual changes, requires knowledge of molecular structures, their interactions, and their conformational dynamics [ 19].
Other genetic activities or molecular structures that are intrinsic to retrotransposons may be required as well.
In QSAR modeling and other cheminformatics applications however, molecular properties are typically calculated using 1D, 2D or 3D representations of molecular structures and thus access to accurate molecular structures is required.
The preparation of the chemical library for docking required different steps to generate accurate 3D molecular structures.
A structural understanding of the CFH mutations required a molecular structure for CFH, however intact CFH has not been crystallised to date.
Geometric models are used for numerous applications that require simple mathematical modeling of objects, such as buildings, industrial parts, and the molecular structures of chemicals.
