1x80: Difference between revisions
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'''Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase''' | '''Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase''' | ||
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==Reference== | ==Reference== | ||
Molecular mechanism for regulation of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex by phosphorylation., Wynn RM, Kato M, Machius M, Chuang JL, Li J, Tomchick DR, Chuang DT, Structure. 2004 Dec;12(12):2185-96. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15576032 15576032] | Molecular mechanism for regulation of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex by phosphorylation., Wynn RM, Kato M, Machius M, Chuang JL, Li J, Tomchick DR, Chuang DT, Structure. 2004 Dec;12(12):2185-96. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15576032 15576032] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
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[[Category: Tomchick, D R.]] | [[Category: Tomchick, D R.]] | ||
[[Category: Wynn, R M.]] | [[Category: Wynn, R M.]] | ||
[[Category: | [[Category: Acylation]] | ||
[[Category: | [[Category: Branched-chain]] | ||
[[Category: | [[Category: Flavoprotein]] | ||
[[Category: | [[Category: Multi-enzyme complex]] | ||
[[Category: | [[Category: Oxidative decarboxylation maple syrup urine disease]] | ||
[[Category: | [[Category: Oxidoreductase,ketoacid dehydrogenase]] | ||
[[Category: | [[Category: Phosphorylation]] | ||
[[Category: | [[Category: Thiamin diphosphate]] | ||
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Revision as of 14:41, 3 May 2008
Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase
OverviewOverview
The human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex (BCKDC) is a 4 MDa macromolecular machine comprising three catalytic components (E1b, E2b, and E3), a kinase, and a phosphatase. The BCKDC overall activity is tightly regulated by phosphorylation in response to hormonal and dietary stimuli. We report that phosphorylation of Ser292-alpha in the E1b active site channel results in an order-to-disorder transition of the conserved phosphorylation loop carrying the phosphoryl serine. The conformational change is triggered by steric clashes of the phosphoryl group with invariant His291-alpha that serves as an indispensable anchor for the phosphorylation loop through bound thiamin diphosphate. Phosphorylation of Ser292-alpha does not severely impede the E1b-dependent decarboxylation of alpha-ketoacids. However, the disordered loop conformation prevents phosphorylated E1b from binding the E2b lipoyl-bearing domain, which effectively shuts off the E1b-catalyzed reductive acylation reaction and therefore completely inactivates BCKDC. This mechanism provides a paradigm for regulation of mitochondrial alpha-ketoacid dehydrogenase complexes by phosphorylation.
DiseaseDisease
Known disease associated with this structure: Maple syrup urine disease, type Ia OMIM:[608348], Maple syrup urine disease, type Ib OMIM:[248611]
About this StructureAbout this Structure
1X80 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
Molecular mechanism for regulation of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex by phosphorylation., Wynn RM, Kato M, Machius M, Chuang JL, Li J, Tomchick DR, Chuang DT, Structure. 2004 Dec;12(12):2185-96. PMID:15576032 Page seeded by OCA on Sat May 3 14:41:14 2008
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCA- Pages with broken file links
- Homo sapiens
- Protein complex
- Chuang, D T.
- Chuang, J L.
- Kato, M.
- Li, J.
- Machius, M.
- Tomchick, D R.
- Wynn, R M.
- Acylation
- Branched-chain
- Flavoprotein
- Multi-enzyme complex
- Oxidative decarboxylation maple syrup urine disease
- Oxidoreductase,ketoacid dehydrogenase
- Phosphorylation
- Thiamin diphosphate