The current understanding of created
"kinds" is related to higher taxonomic orders and it is not easy to
explain or define the created “kinds” like species. Taxonomy is the branch of science in which we study about the
classification of something but mostly it is related to the classification of
organisms.
Answer:
1. Space-filling
2. Ribbon model
3. Wire frame
4. Simple shape
5. Simplified diagram
Explanation:
"attached is the question"
A protein can be visualized using different types of models. The models you use will depend on what you want the viewer to understand. A space-filling model would show all the atoms that composes a protein. This type of model makes use of spheres, emphasizing the globular structure of the atoms. They are proportional to the actual size of the atom they represent. Each type of atom is a different color. Even the distances of the spheres are proportional to its size to help viewers better see the actual shape of the protein. Ribbon model is also a 3D representation of a protein. It shows the only the backbone of the protein. It highlights the folds and coils in a protein, generally the organization. Some versions show the α-helices as ribbons and β-strands are shown as arrows. Wire frame model is like the ribbon model but it also shows the side chains. It shows the different atoms that are involved. Thin wires show the bonds made between the atoms and the wires bend show the relative location of the atoms. A simple shape focuses more on the function of the protein overall rather than the internal structures. The shape does not represent a particular protein, merely using a general shape to represent a protein. A simplified diagram shows more detail than the simple shape. It shows the internal structures as well but like the simple shape model, it focuses more on the function of the protein. A version of it is a solid shape, which does not show the internal structure.
I think the correct answer is C. Hope this helps.
Answer:
B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.
A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.
Explanation:
As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.
The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.
As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.
For the second wig its decreasing
