Both the scientific and colloquial name of the bird are related to its use of human-made structures.
Towards this goal, we first identified possible pockets in the set of Mtb and human structures, using PD, a validated algorithm that was recently developed in our lab.
While basal polarity and growth-arrest are routinely used as features of the differentiation of human epithelial structures in 3D culture, the presence of apical polarity is less often emphasized.
The most common methods used in the study of human population structure are clustering approaches [5] [7] and principal components analysis (PCA) [1], [8], [9].
Two sets of simulations of these three states were performed: the first set using the crystal structure of human CLIC1 as the starting structure and the second set using the same structure, but with the C-terminal residues 234 241 modeled in an α-helical conformation (see below).
For ACAD9 the human structure of ACADVL was used to predict the chameleon structure (PDB 2UXW, unpublished).
Using crystal structures of human Sirt2, 3, 5, and 6, we identified potential ligands for the peptide binding grove through a docking screen with a small molecule library.
In addition to this earlier work, there has been considerable growing attention on simulating the brain dynamics and its relation to self-organized criticality using the structure of human connectome from the DTI based measurements [ 32].
We took advantage of this conservation and used the human crystal structure as a template to generate a ScKrs1 homology model.
The sequence data were used to model the structure of the LDH-b onto the known human structure (Figure 1b, c; and see below).
