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Disorders of metabolism of sulfur-containing amino acids include homocystinuria, cystathionuria, and mercaptolactate-cysteine disulfiduria. These conditions impair the breakdown of methionine and cysteine, leading to the accumulation of toxic metabolites that can cause various symptoms such as intellectual disability, eye lens dislocation, and cardiovascular issues. Treatment typically involves dietary modifications and supplementation of specific nutrients.

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Q: What are the disorders of metabolism of sulphur containing amino acids?
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What has the author R A Chalmers written?

R. A. Chalmers has written: 'L-carnitine in the management of metabolic disorders in children' 'The role of l-carnitine in intermediary metabolism and human metabolic disorders' 'Microprocessors in Analytical Chemistry, Vol. 27' 'Organic acids in man' -- subject(s): Acidosis, Analysis, Carboxylic acids, Clinical chemistry, Diagnosis, Disorders, Inborn Errors Metabolism, Metabolism, Organic acids, Technique


Does bifidobacterium has sulfur chemical in it?

Bifidobacteria are bacteria and all bacteria contain protein. And as all protein containes sulphur-containing amino acids, all living creatures have many sulphur components in them.


How do you compare sulphur content in albumin and egg yolk?

Albumin typically has very low sulphur content compared to egg yolk, as the latter contains a higher concentration of sulphur-containing compounds such as cysteine and methionine. This is because egg yolk serves as a nutrient-rich environment for the developing embryo, requiring a diverse range of essential amino acids, including sulphur-containing ones.


What is the test for sulphur containing amino acids?

The cyanide-nitroprusside test can be used to detect sulphur. The test detects sulphhydryl group compounds and is used to test urine in screening tests for the metabolic diseases, cystinuria and homocystinuria.


Nitrogenous waste is the product of what metabolism?

Nitrogenous waste is the product of protein metabolism in animals, including humans. It is produced as a result of the breakdown of proteins into amino acids, which releases nitrogen-containing compounds that need to be excreted from the body.


What is the difference between amino acids and other acids?

Amino acids are molecules containing both amine and carboxyl functional groups. Amino acids are critical to life, and have a variety of roles in metabolism. One particularly important function is as the building blocks of proteins, which are linear chains of amino acids.


What are some disorders of nucleic acids?

Some disorders of nucleic acids include: Genetic disorders caused by mutations in DNA such as cystic fibrosis, Huntington's disease, and sickle cell anemia. RNA-related disorders like myotonic dystrophy and fragile X syndrome, which are caused by abnormal expansion of nucleotide repeats in the gene. Defects in enzymes involved in nucleic acid metabolism can lead to disorders like Lesch-Nyhan syndrome or SCID (severe combined immunodeficiency).


What is the job of sulfur in the body?

Sulfur is a key component in various amino acids and proteins, helping in the formation of disulfide bonds that contribute to the structure and function of proteins. It is also involved in various metabolic pathways and acts as an antioxidant, protecting cells from damage caused by free radicals.


Do all acids contain sulphur?

No. All acids contain Hydrogen. That is the only component they have in common.


Which molecule is common to the metabolism of carbohydrates fatty acids amino acids and alcohol?

Acetyl-CoA is the molecule common to the metabolism of carbohydrates, fatty acids, amino acids, and alcohol. It serves as a central molecule in cellular metabolism, being the entry point for the citric acid cycle and playing a key role in the production of energy through the metabolism of various nutrients.


Does anti acids have sulfa in them?

Sulphur is acidic, therefore not an ingredient of an antacid.


Which is not a fuel supply for energy in cellular metabolism?

Sunlight is not a fuel supply for energy in cellular metabolism. Common fuel supplies for cellular metabolism include glucose, fatty acids, and amino acids.