Cook W J, Walter L J, Walter M R
Department of Pathology, University of Alabama at Birmingham 35294.
Biochemistry. 1994 Dec 27;33(51):15259-65. doi: 10.1021/bi00255a006.
The crystal structure of calmodulin (CaM) bound to trifluoperazine (TFP) has been determined and refined to a resolution of 2.45 A. Only one TFP is bound to CaM, but that is sufficient to cause distortion of the central alpha-helix and juxtaposition of the N- and C-terminal domains similar to that seen in CaM-polypeptide complexes. The drug makes extensive contacts with residues in the C-terminal domain of CaM but only a few contacts with one residue in the N-terminal domain. The structure suggests that substrate binding to the C-terminal domain is sufficient to cause the conformational changes in calmodulin that lead to activation of its targets.
已确定与三氟拉嗪(TFP)结合的钙调蛋白(CaM)的晶体结构,并将其精修至2.45埃的分辨率。只有一个TFP与CaM结合,但这足以导致中央α-螺旋扭曲以及N端和C端结构域并列,类似于在CaM-多肽复合物中看到的情况。该药物与CaM C端结构域中的残基有广泛接触,但与N端结构域中的一个残基只有少量接触。该结构表明,底物与C端结构域的结合足以引起钙调蛋白的构象变化,从而导致其靶标的激活。