Ma P C, Rould M A, Weintraub H, Pabo C O
Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02139.
Cell. 1994 May 6;77(3):451-9. doi: 10.1016/0092-8674(94)90159-7.
The crystal structure of a MyoD basic-helix-loop-helix (bHLH) domain-DNA complex has been solved and refined at 2.8 A resolution. This structure proves that bHLH and bHLH-leucine zipper (bHLH-ZIP) proteins are remarkably similar; it helps us understand subtle differences in binding preferences for these proteins; and it has surprising implications for our understanding of transcription. Specifically, Ala-114 and Thr-115, which are required for positive control in the myogenic proteins, are buried at the protein-DNA interface. These residues are not available for direct protein-protein contacts, but they may determine the conformation of Arg-111. Comparisons with Max suggest that the conformation of this arginine, which is different in the two structures, may play an important role in myogenic transcription.
肌分化因子(MyoD)碱性螺旋-环-螺旋(bHLH)结构域与DNA复合物的晶体结构已被解析,并在2.8埃分辨率下进行了精修。该结构证明bHLH蛋白和bHLH-亮氨酸拉链(bHLH-ZIP)蛋白非常相似;有助于我们理解这些蛋白在结合偏好上的细微差异;并且对我们理解转录有着惊人的启示。具体而言,在肌源性蛋白中对正向调控所必需的丙氨酸-114和苏氨酸-115,埋藏在蛋白质与DNA的界面处。这些残基无法用于直接的蛋白质-蛋白质接触,但它们可能决定精氨酸-111的构象。与Max的比较表明,这个精氨酸在两种结构中不同的构象,可能在肌源性转录中起重要作用。