Krengel U, Schlichting I, Scherer A, Schumann R, Frech M, John J, Kabsch W, Pai E F, Wittinghofer A
Max-Planck-Institut für medizinische Forschung Abteilung Biophysik, Heidelberg, Federal Republic of Germany.
Cell. 1990 Aug 10;62(3):539-48. doi: 10.1016/0092-8674(90)90018-a.
The X-ray structures of the guanine nucleotide binding domains (amino acids 1-166) of five mutants of the H-ras oncogene product p21 were determined. The mutations described are Gly-12----Arg, Gly-12----Val, Gln-61----His, Gln-61----Leu, which are all oncogenic, and the effector region mutant Asp-38----Glu. The resolutions of the crystal structures range from 2.0 to 2.6 A. Cellular and mutant p21 proteins are almost identical, and the only significant differences are seen in loop L4 and in the vicinity of the gamma-phosphate. For the Gly-12 mutants the larger side chains interfere with GTP binding and/or hydrolysis. Gln-61 in cellular p21 adopts a conformation where it is able to catalyze GTP hydrolysis. This conformation has not been found for the mutants of Gln-61. Furthermore, Leu-61 cannot activate the nucleophilic water because of the chemical nature of its side chain. The D38E mutation preserves its ability to bind GAP.
测定了H-ras癌基因产物p21的五个突变体的鸟嘌呤核苷酸结合结构域(氨基酸1-166)的X射线结构。所描述的突变包括Gly-12→Arg、Gly-12→Val、Gln-61→His、Gln-61→Leu,这些都是致癌突变,以及效应区突变体Asp-38→Glu。晶体结构的分辨率在2.0至2.6埃之间。细胞型和突变型p21蛋白几乎相同,唯一显著的差异出现在环L4和γ-磷酸附近。对于Gly-12突变体,较大的侧链会干扰GTP结合和/或水解。细胞型p21中的Gln-61采取一种能够催化GTP水解的构象。在Gln-61的突变体中未发现这种构象。此外,由于其侧链的化学性质,Leu-61无法激活亲核水。D38E突变保留了其结合GAP的能力。