Furois-Corbin S, Pullman A
Institut de Biologie Physico-Chimique, C.N.R.S., Paris, France.
Biochim Biophys Acta. 1988 Oct 20;944(3):399-413. doi: 10.1016/0005-2736(88)90511-1.
Energy optimizations are carried out on the N-terminal fragment of trichorzianine in comparison to that of alamethicin. The results indicate that the helical character of the (Ac...Pro13) sequence of trichorzianine (TA IIIc) is essentially alpha with a bend in the helix axis in the end proline region, a structure comparable to the optimal alpha-helical structure of the corresponding segment (Ac...Pro14) of alamethicin AI. However, two weak n----n + 3 interactions coexist in trichorzianine with the alpha-helical n----n + 4 hydrogen bonds. The possible role of the glutamine side-chains in pairing such segments together is considered.
与短杆菌肽相比,对曲古抑菌素的N端片段进行了能量优化。结果表明,曲古抑菌素(TA IIIc)的(Ac...Pro13)序列的螺旋特征基本上是α螺旋,在脯氨酸末端区域的螺旋轴上有一个弯曲,该结构与短杆菌肽AI相应片段(Ac...Pro14)的最佳α螺旋结构相当。然而,在曲古抑菌素中,两个弱的n----n + 3相互作用与α螺旋的n----n + 4氢键共存。考虑了谷氨酰胺侧链在将这些片段配对在一起时可能发挥的作用。