Turkenburg Johan P, Lamers Marieke B A C, Brzozowski A Marek, Wright Lisa M, Hubbard Roderick E, Sturt Simone L, Williams David H
York Structural Biology Laboratory, Chemistry Department, University of York, Heslington, York YO10 5DD, England.
Acta Crystallogr D Biol Crystallogr. 2002 Mar;58(Pt 3):451-5. doi: 10.1107/s0907444901021825. Epub 2002 Feb 21.
Cathepsin S (EC 3.4.22.27), a cysteine proteinase of the papain superfamily, plays a critical role in the generation of a major histocompatibility complex (MHC) class II restricted T-cell response by antigen-presenting cells. Therefore, selective inhibition of this enzyme may be useful in modulating class II restricted T-cell responses in immune-related disorders such as rheumatoid arthritis, multiple sclerosis and extrinsic asthma. The three-dimensional structure at 2.2 A resolution of the active-site Cys25-->Ser mutant presented here in an unliganded state provides further insight useful for the design of selective enzyme inhibitors.
组织蛋白酶S(EC 3.4.22.27)是木瓜蛋白酶超家族的一种半胱氨酸蛋白酶,在抗原呈递细胞产生主要组织相容性复合体(MHC)II类限制性T细胞应答过程中发挥关键作用。因此,选择性抑制该酶可能有助于调节免疫相关疾病(如类风湿性关节炎、多发性硬化症和外源性哮喘)中的II类限制性T细胞应答。此处展示的处于未结合状态的活性位点Cys25→Ser突变体在2.2埃分辨率下的三维结构,为选择性酶抑制剂的设计提供了更有用的见解。