Valine—pyruvate transaminase

From WikiMD's medical encyclopedia

Valine—pyruvate transaminase is an enzyme that catalyzes the chemical reaction between L-valine and pyruvate. This reaction is a part of the amino acid metabolism, specifically involved in the catabolism of branched-chain amino acids such as valine, which is crucial for energy production and synthesis of cellular components in various organisms.

Function

Valine—pyruvate transaminase facilitates the transfer of an amino group from L-valine, an essential amino acid, to pyruvate, a key intermediate in the glycolysis pathway, forming alpha-ketoisovalerate and L-alanine. This reaction is reversible and plays a significant role in the metabolic pathway that breaks down amino acids for energy production. The enzyme is part of the transaminase family, which is involved in the transfer of amino groups between amino acids and alpha-keto acids.

Structure

The structure of valine—pyruvate transaminase, like other transaminases, typically consists of a protein with a pyridoxal phosphate (PLP) cofactor attached. The PLP is essential for the enzyme's activity, acting as a carrier of amino groups during the transamination process. The enzyme's structure allows it to bind both substrates (L-valine and pyruvate) and facilitate the efficient transfer of the amino group.

Clinical Significance

Alterations in the activity of valine—pyruvate transaminase can have clinical implications, particularly in disorders related to amino acid metabolism such as Maple Syrup Urine Disease (MSUD). MSUD is a metabolic disorder characterized by a deficiency in the enzyme complex responsible for the catabolism of branched-chain amino acids, leading to an accumulation of these amino acids and their toxic by-products. Monitoring the activity of enzymes like valine—pyruvate transaminase can be crucial in the diagnosis and management of such conditions.

Genetic Regulation

The expression of the gene encoding valine—pyruvate transaminase is regulated by various factors, including nutritional status and hormonal signals. This regulation ensures that the enzyme's activity is modulated according to the body's metabolic needs, particularly in response to dietary intake of amino acids and energy demand.

See Also

References


Stub icon
   This article is a biochemistry stub. You can help WikiMD by expanding it!



Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Transform your life with W8MD's budget GLP-1 injections from $125.

W8mdlogo.png
W8MD weight loss doctors team

W8MD offers a medical weight loss program to lose weight in Philadelphia. Our physician-supervised medical weight loss provides:

NYC weight loss doctor appointments

Start your NYC weight loss journey today at our NYC medical weight loss and Philadelphia medical weight loss clinics.

Linkedin_Shiny_Icon Facebook_Shiny_Icon YouTube_icon_(2011-2013) Google plus


Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD