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Non-discriminating and discriminating aspartyl-tRNA synthetases differ in the anticodon-binding domain

机译:非区分性和区分性天冬氨酰-tRNA合成酶在反密码子结合域方面有所不同

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摘要

In most organisms, tRNA aminoacylation is ensured by 20 aminoacyl-tRNA synthetases (aaRSs). In eubacteria, however, synthetases can be duplicated as in Thermus thermophilus, which contains two distinct AspRSs. While AspRS-1 is specific, AspRS-2 is non-discriminating and aspartylates tRNAAsp and tRNAAsn. The structure at 2.3 Å resolution of AspRS-2, the first of a non-discriminating synthetase, was solved. It differs from that of AspRS-1 but has resemblance to that of discriminating and archaeal AspRS from Pyrococcus kodakaraensis. The protein presents non-conventional features in its OB-fold anticodon-binding domain, namely the absence of a helix inserted between two β-strands of this fold and a peculiar L1 loop differing from the large loops known to interact with tRNAAsp identity determinant C36 in conventional AspRSs. In AspRS-2, this loop is small and structurally homologous to that in AsnRSs, including conservation of a proline. In discriminating Pyrococcus AspRS, the L1 loop, although small, lacks this proline and is not superimposable with that of AspRS-2 or AsnRS. Its particular status is demonstrated by a loop-exchange experiment that renders the Pyrococcus AspRS non-discriminating.
机译:在大多数生物中,通过20种氨酰基-tRNA合成酶(aaRSs)确保tRNA氨酰化。但是,在真细菌中,合成酶可以像嗜热菌(Thermus thermophilus)一样复制,其中包含两个不同的AspRS。尽管AspRS-1是特异性的,但AspRS-2却是非歧视性的,可以使tRNA Asp 和tRNA Asn 天冬酰胺化。解决了第一个非歧视性合成酶AspRS-2在2.3Å分辨率下的结构。它不同于AspRS-1,但与区分和古柯热球菌的古细菌AspRS相似。该蛋白质在其OB折叠反密码子结合结构域中表现出非常规特征,即在此折叠的两个β链之间不插入螺旋,并且没有一个独特的L1环,该环不同于已知与tRNA相互作用的大环。传统AspRSs中Asp 同一性决定因素C36。在AspRS-2中,此环很小,在结构上与AsnRS中的环同源,包括脯氨酸的保守。在区分火球菌AspRS时,L1环虽然很小,但缺少脯氨酸,并且不能与AspRS-2或AsnRS重叠。它的特殊状态通过循环交换实验得以证明,该实验使热球菌AspRS不受歧视。

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