Fukunaga Ryuya, Yokoyama Shigeyuki
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
J Mol Biol. 2007 Jun 29;370(1):128-41. doi: 10.1016/j.jmb.2007.04.050. Epub 2007 May 4.
In the ancient organisms, methanogenic archaea, lacking the canonical cysteinyl-tRNA synthetase, Cys-tRNA(Cys) is produced by an indirect pathway, in which O-phosphoseryl-tRNA synthetase ligates O-phosphoserine (Sep) to tRNA(Cys) and Sep-tRNA:Cys-tRNA synthase (SepCysS) converts Sep-tRNA(Cys) to Cys-tRNA(Cys). In this study, the crystal structure of SepCysS from Archaeoglobus fulgidus has been determined at 2.4 A resolution. SepCysS forms a dimer, composed of monomers bearing large and small domains. The large domain harbors the seven-stranded beta-sheet, which is typical of the pyridoxal 5'-phosphate (PLP)-dependent enzymes. In the active site, which is located near the dimer interface, PLP is covalently bound to the side-chain of the conserved Lys209. In the proximity of PLP, a sulfate ion is bound by the side-chains of the conserved Arg79, His103, and Tyr104 residues. The active site is located deep within the large, basic cleft to accommodate Sep-tRNA(Cys). On the basis of the surface electrostatic potential, the amino acid residue conservation mapping, the position of the bound sulfate ion, and the substrate amino acid binding manner in other PLP-dependent enzymes, a binding model of Sep-tRNA(Cys) to SepCysS was constructed. One of the three strictly conserved Cys residues (Cys39, Cys42, or Cys247), of one subunit may play a crucial role in the catalysis in the active site of the other subunit.
在古代生物中,产甲烷古菌缺乏典型的半胱氨酰 - tRNA合成酶,其半胱氨酰 - tRNA(Cys)通过间接途径产生,即O - 磷酸丝氨酰 - tRNA合成酶将O - 磷酸丝氨酸(Sep)连接到tRNA(Cys)上,然后Sep - tRNA:半胱氨酰 - tRNA合成酶(SepCysS)将Sep - tRNA(Cys)转化为半胱氨酰 - tRNA(Cys)。在本研究中,已确定来自嗜热栖热菌的SepCysS的晶体结构,分辨率为2.4埃。SepCysS形成二聚体,由具有大小结构域的单体组成。大结构域包含七股β - 折叠,这是依赖于磷酸吡哆醛(PLP)的酶的典型特征。在位于二聚体界面附近的活性位点中,PLP与保守的Lys209的侧链共价结合。在PLP附近,一个硫酸根离子由保守的Arg79、His103和Tyr104残基的侧链结合。活性位点位于大的碱性裂缝深处,以容纳Sep - tRNA(Cys)。基于表面静电势、氨基酸残基保守性图谱、结合的硫酸根离子的位置以及其他依赖PLP的酶中底物氨基酸的结合方式,构建了Sep - tRNA(Cys)与SepCysS的结合模型。一个亚基的三个严格保守的半胱氨酸残基(Cys39、Cys42或Cys247)之一可能在另一个亚基的活性位点催化中起关键作用。