Sandbox Reserved 1544

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== Disease ==
== Disease ==
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Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is a disorder dealing with fatty acid oxidation and can be characterized by hypoglycemic crisis during stressful conditions. MCADD is the most common metabolic defect of fatty acid oxidation. Medium-chain acyl-CoA dehydrogenase is a flavoprotein that catalyzes the first reaction in 𝛽-oxidation of fatty acids. The resulting effects include a decrease of ketone production and an increase in medium-chain fatty acid concentration.
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Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is a disorder that affects fatty acid oxidation and can be characterized by a hypoglycemic crisis during times of increased stressed. This deficiency is the most common metabolic defect of fatty acid oxidation. MCADD is a flavoprotein that catalyzes the first reaction in 𝛽-oxidation of fatty acids. Such metabolic reactions are necessary for energy production, especially during periods of fasting. Expression of MCADD results in a decrease of ketone production and an increase in medium-chain fatty acid concentration.
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MCADD is passed genetically through an autosomal recessive trait and it is caused by mutations in the medium-chain acyl- CoA dehydrogenase (ACADM) gene. The ACADM gene is located on chromosome 1p31.
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MCADD is a disorder inherited genetically through an autosomal recessive trait, and it is caused by mutations in the medium-chain acyl- CoA dehydrogenase (ACADM) gene. The ACADM gene is located on chromosome 1p31. There are over 90 different ACADM gene mutations known so far, most of which are missense mutations.
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The disorder can lead to symptoms such as a loss in appetite as well as vomiting and diarrhea. This can result in accumulated concentrations of acylcarnitine, which can be potentially toxic. People who are affected and not diagnosed are at a high risk of dying or experiencing permanent neurological damage during their first metabolic crisis. To prevent such events, immediate care should follow catabolic stress and fasting should be averted. Individuals living with MCADD are asymptomatic up until there is an increased demand for energy followed by a prolonged time of fasting. Newborn screening is now widely implemented through the use of liquid chromatography-tandem mass spectrometry.
== Relevance ==
== Relevance ==

Revision as of 16:14, 8 April 2019

This Sandbox is Reserved from May 28 through July 01, 2019 for use in the course Advanced Biochemistry BCHM 4100 taught by Tom Gluick at the Georgia Gwinnett College. This reservation includes Sandbox Reserved 1544 through Sandbox Reserved 1555.
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Structure

Acyl CoA Dehydrogenase

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References

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
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