• A PYRIDOXAL PHOSPHATE containing enzyme that catalyzes the reversible transamination of branched-chain AMINO ACIDS to 2-oxoglutarate. (lookformedical.com)
  • The enzyme deficient in MSUD, the branched-chain alpha-keto acid dehydrogenase (BCKAD) complex, is a mitochondrial multienzyme complex consisting of at least six distinct subunits. (nih.gov)
  • This gene encodes the E2 subunit of the branched-chain α-keto acid dehydrogenase (BCKDH) complex, a core component of branched-chain amino acid (BCAA) metabolism. (nih.gov)
  • Our study implicates the BCKDH complex and BCAA metabolism in arsenic responses, demonstrating the power of C. elegans natural genetic diversity to identify novel mechanisms by which environmental toxins affect organismal physiology.This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. (nih.gov)
  • Catalyzes the phosphorylation and inactivation of the branched-chain alpha-ketoacid dehydrogenase complex, the key regulatory enzyme of the valine, leucine and isoleucine catabolic pathways. (nih.gov)
  • The branched-chain alpha-ketoacid dehydrogenase complex (BCKD) is an important regulator of the valine, leucine, and isoleucine catabolic pathways. (nih.gov)
  • 10/2/2003) TOTAL DESCRIPTORS = 666 MH - Acalculous Cholecystitis UI - D042101 MN - C6.130.564.263.249 MS - Inflammation of the GALLBLADDER wall in the absence of GALLSTONES. (nih.gov)
  • part of family of 3'-to5' exonucleases. (lbl.gov)