Rould M A, Perona J J, Söll D, Steitz T A
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511.
Science. 1989 Dec 1;246(4934):1135-42. doi: 10.1126/science.2479982.
The crystal structure of Escherichia coli glutaminyl-tRNA synthetase (GlnRS) complexed with its cognate glutaminyl transfer RNA (tRNA(Gln] and adenosine triphosphate (ATP) has been derived from a 2.8 angstrom resolution electron density map and the known protein and tRNA sequences. The 63.4-kilodalton monomeric enzyme consists of four domains arranged to give an elongated molecule with an axial ratio greater than 3 to 1. Its interactions with the tRNA extend from the anticodon to the acceptor stem along the entire inside of the L of the tRNA. The complexed tRNA retains the overall conformation of the yeast phenylalanine tRNA (tRNA(Phe] with two major differences: the 3' acceptor strand of tRNA(Gln) makes a hairpin turn toward the inside of the L, with the disruption of the final base pair of the acceptor stem, and the anticodon loop adopts a conformation not seen in any of the previously determined tRNA structures. Specific recognition elements identified so far include (i) enzyme contacts with the 2-amino groups of guanine via the tRNA minor groove in the acceptor stem at G2 and G3; (ii) interactions between the enzyme and the anticodon nucleotides; and (iii) the ability of the nucleotides G73 and U1.A72 of the cognate tRNA to assume a conformation stabilized by the protein at a lower free energy cost than noncognate sequences. The central domain of this synthetase binds ATP, glutamine, and the acceptor end of the tRNA as well as making specific interactions with the acceptor stem.2+t is
大肠杆菌谷氨酰胺-tRNA合成酶(GlnRS)与其同源谷氨酰胺转移RNA(tRNA(Gln])及三磷酸腺苷(ATP)形成的复合物的晶体结构,是根据分辨率为2.8埃的电子密度图以及已知的蛋白质和tRNA序列推导出来的。这种63.4千道尔顿的单体酶由四个结构域组成,排列成一个轴向比大于3比1的细长分子。它与tRNA的相互作用从反密码子延伸到受体茎,沿着tRNA的L形结构的整个内侧。结合后的tRNA保留了酵母苯丙氨酸tRNA(tRNA(Phe])的整体构象,但有两个主要区别:tRNA(Gln)的3'受体链向L形结构内部形成一个发夹弯,受体茎的最后一对碱基对被破坏,并且反密码子环采用了在任何先前确定的tRNA结构中都未见过的构象。目前已确定的特异性识别元件包括:(i)酶通过受体茎中G2和G3处的tRNA小沟与鸟嘌呤的2-氨基接触;(ii)酶与反密码子核苷酸之间的相互作用;(iii)同源tRNA的核苷酸G73和U1.A72能够以比非同源序列更低的自由能成本形成由蛋白质稳定的构象。这种合成酶的中央结构域结合ATP、谷氨酰胺和tRNA的受体末端,并与受体茎进行特异性相互作用。2+t是