Hart P A, Marshall C J
Institute of Cancer Research, Chester Beatty Laboratories, London, UK.
Oncogene. 1990 Jul;5(7):1099-101.
The GTPase activating protein (ras-GAP) has been shown to interact with p21ras at a domain defined by amino acids 32-40. The sequences of the rap family of ras related proteins (including a suppressor of ras transformation Krev-1/rap1A) are identical to ras in this region. Incubation of rap1A protein with ras-GAP does not accelerate the rate of GTP hydrolysis by p21rap1A. Rap proteins have threonine at amino acid 61, whereas ras proteins have glutamine at this site and mutation to threonine reduces the intrinsic GTPase of p21ras. We have, therefore, mutated thr61 of p21rap1A to glutamine and shown that ras-GAP is now able to accelerate the rate of hydrolysis of GTP. This demonstrates that ras-GAP can interact with rap and that the sensitivity to ras-GAP is determined in part by the amino acid at codon 61.
GTP酶激活蛋白(ras-GAP)已被证明可在由氨基酸32 - 40定义的结构域与p21ras相互作用。ras相关蛋白rap家族(包括ras转化抑制因子Krev-1/rap1A)的序列在该区域与ras相同。将rap1A蛋白与ras-GAP一起孵育并不会加速p21rap1A的GTP水解速率。Rap蛋白在氨基酸61处为苏氨酸,而ras蛋白在该位点为谷氨酰胺,突变为苏氨酸会降低p21ras的内在GTP酶活性。因此,我们将p21rap1A的thr61突变为谷氨酰胺,结果表明ras-GAP现在能够加速GTP的水解速率。这证明ras-GAP可与rap相互作用,并且对ras-GAP的敏感性部分由密码子61处的氨基酸决定。