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Annual Review of Biochemistry 6: 41-66.Google Scholar REBOUCHE, C.J

Crystal structure of BDK shows that an allosteric inhibitor such as (S)--chloro-phenylpropionic acid [(S)-CPP] binds to a site in the N-terminal domain to cause a movement of the helix-bundle and a conformational change in BDK to promote full activation and dephosphorylation of BCKDH (Figure 7) (Popov et al., 1991

Johnson et al., 2019), limited information is available regarding bioenergetics within the cerebrovasculature, particularly in relation to both FA uptake and fatty acid oxidation (FAO) capabilities within the context of aging and different APOE genotypes, despite the fact that cerebrovascular FAO has been suggested to be an essential process in maintaining its transport functions (Goldstein, 1979)

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