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  2. Pyruvate dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase

    Decreased activity of mitochondrial PDH with age has been shown in the heart as well as in certain regions of the brain (the striatum and brainstem). [6] Pyruvate dehydrogenase (PDH) deficiency is a congenital degenerative metabolic disease resulting from a mutation of the pyruvate dehydrogenase complex (PDC) located on the X chromosome.

  3. Pyruvate dehydrogenase complex - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_complex

    In eukaryotic cells the pyruvate decarboxylation occurs inside the mitochondrial matrix, after transport of the substrate, pyruvate, from the cytosol. The transport of pyruvate into the mitochondria is via the transport protein pyruvate translocase. Pyruvate translocase transports pyruvate in a symport fashion with a proton (across the inner ...

  4. Pyruvate dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase...

    They cannot, however, supply ATP to these cells and, therefore, phenotype depends largely on the nature/severity of the mutation. [5] [8] More rarely, mutations occur in the E2 (dihydrolipoyl transacetylase) or the E3 (dihydrolipoyl dehydrogenase) subunits of the PDC enzymatic complex, DLAT and DLD genes respectively. In these cases, PDCD ...

  5. Pyruvate dehydrogenase (lipoamide) alpha 1 - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_(l...

    Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial is an enzyme that in humans is encoded by the PDHA1 gene.The pyruvate dehydrogenase complex is a nuclear-encoded mitochondrial matrix multienzyme complex that provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle by catalyzing the irreversible conversion of pyruvate into acetyl-CoA.

  6. Pyruvate dehydrogenase kinase - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_kinase

    The primary sequencing between the four isozymes are conserved with 70% identity. The greatest differences occur near the N-terminus. [2] PDK1 is the largest of the four with 436 residues while PDK2, PDK3 and PDK4 have 407, 406, and 411 residues respectively. The isozymes have different activity and phosphorylation rates at each site.

  7. Pyruvate dehydrogenase (lipoamide) beta - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_dehydrogenase_(l...

    The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 beta subunit.

  8. The Nervous Mechanism of Plants - Wikipedia

    en.wikipedia.org/.../The_Nervous_Mechanism_of_Plants

    “The Nervous Mechanism of Plants”, published in 1926, is a botany book by Sir Jagadish Chandra Bose which summarises his most recent findings in the area of plant physiology. Bose had previously investigated this topic in books such as Plant response as a means of physiological investigation from 1906, or The physiology of photosynthesis ...

  9. Oxoglutarate dehydrogenase complex - Wikipedia

    en.wikipedia.org/wiki/Oxoglutarate_dehydrogenase...

    Stress in cells can cause a deregulation in the biosynthesis of the neurotransmitter glutamate. Glutamate toxicity in the brain is caused by a buildup of glutamate under times of stress. If oxoglutarate dehydrogenase activity is dysfunctional (no adaptive stress compensation), the build-up of glutamate cannot be fixed, and brain pathologies can ...