Abstract
2-oxo acid dehydrogenase complexes are a ubiquitous family of multienzyme systems that catalyse the oxidative decarboxylation of various 2-oxo acid substrates. They play a key role in the primary energy metabolism: in glycolysis (pyruvate dehydrogenase complex), the citric acid cycle (2-oxoglutarate dehydrogenase complex) and in amino acid catabolism (branched-chain 2-oxo acid dehydrogenase complex). Malfunctioning of any of these complexes leads to a broad variety of clinical mani-festations. Deficiency of the pyruvate dehydrogenase complex predominantly leads to lactic acidosis combined with impairment of neurological function and / or delayed growth and development. Maple urine disease is an inborn metabolic error caused by dysfunction of the branched-chain 2-oxo acid dehydrogenase complex. An association between both Alzheimer disease and Parkinsons disease and the 2-oxoglutarate dehydrogenase gene has been reported. Currently a wealth of both genetic and structural information is available. Three-dimensional structures of three components of the complex are presently available: of the pyruvate dehydrogenase component (E1), of the dihydrolipoyl acyltransferase component (E2) and of the lipoamide dehydrogenase component (E3). Moreover, detailed information on the reaction mechanism, regulation and the interactions between the different components of the complex is now at hand. Although only one of the structures is of human origin (E1b), model building by homology modelling allows us to investigate the causes of dysfunction. In this review we have combined this knowledge to gain more insight into the structural basis of the dysfunctioning of the 2-oxo acid dehydrogenase complexes.
Keywords: Human 2-Oxo Acid Dehydrogenase, Alzheimer disease, dihydrolipoamide dehydrogenase component (E3), heterotetrameric, amino-pyrimidine moiety, Protein-Protein Interactions, Dihydrolipoamide dehydrogenase component, Chloramphenicol acetyltransferase, Maple Syrup, Transketolase
Current Medicinal Chemistry
Title: Structural Basis of the Dysfunctioning of Human 2-Oxo Acid Dehydrogenase Complexes
Volume: 9 Issue: 4
Author(s): A. F. Hengeveld and A. de Kok
Affiliation:
Keywords: Human 2-Oxo Acid Dehydrogenase, Alzheimer disease, dihydrolipoamide dehydrogenase component (E3), heterotetrameric, amino-pyrimidine moiety, Protein-Protein Interactions, Dihydrolipoamide dehydrogenase component, Chloramphenicol acetyltransferase, Maple Syrup, Transketolase
Abstract: 2-oxo acid dehydrogenase complexes are a ubiquitous family of multienzyme systems that catalyse the oxidative decarboxylation of various 2-oxo acid substrates. They play a key role in the primary energy metabolism: in glycolysis (pyruvate dehydrogenase complex), the citric acid cycle (2-oxoglutarate dehydrogenase complex) and in amino acid catabolism (branched-chain 2-oxo acid dehydrogenase complex). Malfunctioning of any of these complexes leads to a broad variety of clinical mani-festations. Deficiency of the pyruvate dehydrogenase complex predominantly leads to lactic acidosis combined with impairment of neurological function and / or delayed growth and development. Maple urine disease is an inborn metabolic error caused by dysfunction of the branched-chain 2-oxo acid dehydrogenase complex. An association between both Alzheimer disease and Parkinsons disease and the 2-oxoglutarate dehydrogenase gene has been reported. Currently a wealth of both genetic and structural information is available. Three-dimensional structures of three components of the complex are presently available: of the pyruvate dehydrogenase component (E1), of the dihydrolipoyl acyltransferase component (E2) and of the lipoamide dehydrogenase component (E3). Moreover, detailed information on the reaction mechanism, regulation and the interactions between the different components of the complex is now at hand. Although only one of the structures is of human origin (E1b), model building by homology modelling allows us to investigate the causes of dysfunction. In this review we have combined this knowledge to gain more insight into the structural basis of the dysfunctioning of the 2-oxo acid dehydrogenase complexes.
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Cite this article as:
Hengeveld F. A. and Kok de A., Structural Basis of the Dysfunctioning of Human 2-Oxo Acid Dehydrogenase Complexes, Current Medicinal Chemistry 2002; 9 (4) . https://dx.doi.org/10.2174/0929867023370996
DOI https://dx.doi.org/10.2174/0929867023370996 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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