0
What else can I help you with?
Do protein cause humans to get fat?
Consuming excess calories from any source, including protein, can contribute to weight gain. Protein itself does not directly cause weight gain, but overeating protein-rich foods without accounting for caloric intake can lead to fat accumulation. It's essential to balance protein intake with overall calorie expenditure to maintain a healthy weight.
Acids and bases denature a protein by disrupting?
the protein's structure through the alteration of its hydrogen bonding patterns. Acids can cause protonation of amino acid side chains, while bases can cause deprotonation. These chemical changes can lead to unfolding of the protein and loss of its function.
How does allel cause a trait an organism?
The allele causes a certain type of protein to form
Can a mutation cause a protein to be overexpressed?
Yes, mutations can potentially lead to overexpression of a protein by altering the regulation of gene expression or by affecting the stability of the protein. Mutations that occur in the regulatory regions of a gene can disrupt the normal control mechanisms, resulting in increased production of the protein.
Mutations that cause dramatic changes in protein structure are often?
Mutations that cause dramatic changes in protein structure are often deleterious and can lead to dysfunctional or nonfunctional proteins. These mutations can disrupt the overall folding, stability, and function of the protein, resulting in a loss of its normal biological activity or causing harmful effects on the organism.
What type of chemical is fibrillin?
Protein
What is the abnormal protein in Marfan's syndrome?
connective tissue protein fibrillin-1.
What is a Marfan Syndrome?
marfan syndrome is genetic disorder of connective tissue of the body. it cause a mutation of the gene that produces the protein fibrillin.
What is fibrillin?
Fibrillin is a glycoprotein, which is essential for the formation of elastic fibers found in connective tissue.[1] Fibrillin-1 is a major component of the microfibrils that form a sheath surrounding the amorphous elastin. It is believed that the microfibrils are composed of end-to-end polymers of fibrillin. To date, 3 forms of fibrillin have been described. The fibrillin-1 protein was isolated by Sakai in 1986,[2] and mutations in the gene have been linked to the Marfan syndrome. At present more than 100 different mutations have been described. Fibrillin-2 was isolated in 1994 by Zhang[3] and is thought to play a role in early elastogenesis. Mutations in the fibrillin-2 gene have been linked to Beal's Syndrome. More recently, fibrillin-3 was described and is believed to be located mainly in the brain.[4] Along with in the brain, fibrillin 1 has been localized in the gonads and ovaries of field mice.
What effect does Marfan syndrome have on the body?
It affects the body's production of fibrillin, which is a protein that is an important part of connective tissue.
What type of mutation causes marfan syndrome?
Marfan syndrome is typically caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. These mutations can result in the production of an abnormal fibrillin-1 protein, leading to the characteristic features of Marfan syndrome such as tall stature, long limbs, and cardiovascular issues.
What chromosome is gene located for marfan syndrome?
The gene associated with Marfan syndrome is located on chromosome 15. It is called the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Mutations in this gene can lead to the characteristic features of Marfan syndrome.
Does marfan syndrome affect the aorta?
Yes. Marfan syndrome is a congenital disorder affecting the formation of fibrillin. In Marfan syndrome, the abnormal fibrillin is responsible for many of the findings of the disease. Hyperextensibility/hyperelasticity of joints is one of the hallmark signs. Pectus excavatum is another. People with Marfan syndrome are typically very tall and thin, with very long fingers and toes (arachnodactyly). The fibrillin defect also affects the blood vessels, especially the large arteries, such as the aorta. Disordered fibrillin production causes these arteries to be weaker than normal, predisposing patients with Marfan syndrome to aortic dissections and rupture. This the major cause of death for patients with Marfan syndrome.
Why is it not possible to use the FBNI gene to diagnose Marfan syndrome?
The FBNI gene encodes for a protein called fibrillin-1, mutations of which are associated with Marfan syndrome. However, there are other genes also implicated in Marfan syndrome. Therefore, diagnosing Marfan syndrome solely based on FBNI gene mutations may not capture the full spectrum of genetic variations that can cause the condition. A comprehensive genetic testing panel is usually needed for an accurate diagnosis.
Can herpes cause high protein in blood?
Herpes does not cause high protein in the blood.
What is the name of the disease caused by not eating enough protein?
A lack of protein does not cause an eating disorder. Instead, that can cause anemia.
Is protein a mineral?
Is Mineral A Protein would be a real question cause MINERALS ARE A PROTEIN!
