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December 1, 1992Journal of Biological ChemistryOpen Access

Impaired tetramer assembly of variant medium-chain acyl-coenzyme A dehydrogenase with a glutamate or aspartate substitution for lysine 304 causing instability of the protein.

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Authors

IYIchiro YokotaShinshu UniversityTSTakahiko SaijoCentre for Advancing Health OutcomesJVJerry VockleyUniversity of Pittsburgh

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Cite This Study

Yokota et al. (1992) studied this question.

synapsesocial.com/papers/6a97e0c3cb7f2a2edc74cd39https://doi.org/10.1016/s0021-9258(18)35708-9
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation.1990 · 102 citations
  2. 2Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzyme-deficient human tissue.1987 · 122 citations
  3. 3Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat liver medium chain acyl coenzyme A dehydrogenase.1987 · 72 citations