Anselme J, Härtlein M
European Molecular Biology Laboratory, Grenoble, France.
FEBS Lett. 1991 Mar 11;280(1):163-6. doi: 10.1016/0014-5793(91)80228-u.
Sequence comparisons of the E. coli asparaginyl-tRNA synthetase (NRSEC) with aminocyl-tRNA synthetase sequences of class II enzymes show significant homologies with aspartyl- and lysyl-tRNA synthetases. Three conserved regions were found, one of which is located in the C-terminal part of the NRSEC sequence. Site-directed mutagenesis was performed in this conserved region. A single point mutation Tyr-426----Ser results in a 15-fold increase in the Km for ATP, while all the other kinetic parameters remain unchanged. The replacement of this Tyr-426 by a Phe does not affect the kinetic behaviour of the enzyme. These data indicate that Tyr-426 is part of the ATP binding site.
将大肠杆菌天冬酰胺-tRNA合成酶(NRSEC)与II类酶的氨酰-tRNA合成酶序列进行序列比较,发现它与天冬氨酸和赖氨酰-tRNA合成酶有显著的同源性。发现了三个保守区域,其中一个位于NRSEC序列的C末端部分。在这个保守区域进行了定点诱变。单点突变Tyr-426→Ser导致ATP的Km增加15倍,而所有其他动力学参数保持不变。用苯丙氨酸取代这个Tyr-426不会影响该酶的动力学行为。这些数据表明Tyr-426是ATP结合位点的一部分。