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2013;144(5):S999

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

Chung B, Segrest J, Smith K, Griffin F, Brouillette C

Olykor, ezek tartalmazhatnak tves informcikat: a kpek tjkoztat jellegek s tartalmazhatnak tartozkokat, amelyek nem szerepelnek az alapcsomagban, egyes lersok vagy az rak elzetes rtests nlkl megvltozhatnak a gyrtk ltal, vagy hibkat tartalmazhatnak

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