Lawrence M C, Pilling P A, Epa V C, Berry A M, Ogunniyi A D, Paton J C
Biomolecular Research Institute 343 Royal Parade Parkville Victoria 3052 Australia.
Structure. 1998 Dec 15;6(12):1553-61. doi: 10.1016/s0969-2126(98)00153-1.
. The surface protein PsaA of the pathogenic bacterium Streptococcus pneumoniae plays an essential role in its virulence. PsaA is a putative ATP-binding cassette-type (ABC-type) binding protein involved in the uptake of Mn2+ and possibly Zn2+ and is considered to be both a potential drug target and and a candidate vaccine component.
. The structure of PsaA has been determined to 2.0 A resolution using X-ray crystallography and is the first structure obtained for an ABC-type binding protein from a Gram-positive organism. The protein consists of two (beta/alpha)4 domains linked together by a single helix. A metal-binding site is formed in the domain interface by the sidechains of His67, His139, Glu205 and Asp280 and is occupied in the structure.
. The structural topology of PsaA is fundamentally different from that of other ABC-type binding proteins determined thus far in that PsaA lacks the characteristic 'hinge peptides' involved in conformational change upon solute uptake and release. In our structure, the metal-binding site is probably occupied by Zn2+. The site seems to be well conserved amongst related receptors from both Gram-positive and Gram-negative bacteria.
致病细菌肺炎链球菌的表面蛋白PsaA在其毒力中起关键作用。PsaA是一种假定的ATP结合盒式(ABC型)结合蛋白,参与锰离子(可能还有锌离子)的摄取,被认为既是潜在的药物靶点又是候选疫苗成分。
利用X射线晶体学已将PsaA的结构解析到2.0埃分辨率,这是从革兰氏阳性菌获得的ABC型结合蛋白的首个结构。该蛋白由两个(β/α)4结构域通过单个螺旋连接在一起组成。在结构域界面由His67、His139、Glu205和Asp280的侧链形成一个金属结合位点,且该位点在结构中被占据。
PsaA的结构拓扑与迄今已确定的其他ABC型结合蛋白根本不同,因为PsaA缺乏在溶质摄取和释放时参与构象变化的特征性“铰链肽”。在我们的结构中,金属结合位点可能被锌离子占据。该位点在革兰氏阳性菌和革兰氏阴性菌的相关受体中似乎高度保守。