1x80: Difference between revisions

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[[Image:1x80.gif|left|200px]]
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{{STRUCTURE_1x80|  PDB=1x80  |  SCENE=  }}  
{{STRUCTURE_1x80|  PDB=1x80  |  SCENE=  }}  


'''Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase'''
===Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase===




==Overview==
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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.
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==Disease==
==Disease==
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[[Category: Phosphorylation]]
[[Category: Phosphorylation]]
[[Category: Thiamin diphosphate]]
[[Category: Thiamin diphosphate]]
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Revision as of 17:53, 28 July 2008

File:1x80.png

Template:STRUCTURE 1x80

Crystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenaseCrystal structure of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase

Template:ABSTRACT PUBMED 15576032

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

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