Bycroft M, Bateman A, Clarke J, Hamill S J, Sandford R, Thomas R L, Chothia C
MRC Centre for Protein Engineering, Lensfield Road, Cambridge CB2 1EW.
EMBO J. 1999 Jan 15;18(2):297-305. doi: 10.1093/emboj/18.2.297.
Most cases of autosomal dominant polycystic kidney disease (ADPKD) are the result of mutations in the PKD1 gene. The PKD1 gene codes for a large cell-surface glycoprotein, polycystin-1, of unknown function, which, based on its predicted domain structure, may be involved in protein-protein and protein-carbohydrate interactions. Approximately 30% of polycystin-1 consists of 16 copies of a novel protein module called the PKD domain. Here we show that this domain has a beta-sandwich fold. Although this fold is common to a number of cell-surface modules, the PKD domain represents a distinct protein family. The tenth PKD domain of human and Fugu polycystin-1 show extensive conservation of surface residues suggesting that this region could be a ligand-binding site. This structure will allow the likely effects of missense mutations in a large part of the PKD1 gene to be determined.
大多数常染色体显性多囊肾病(ADPKD)病例是PKD1基因突变的结果。PKD1基因编码一种功能未知的大型细胞表面糖蛋白——多囊蛋白-1,根据其预测的结构域结构,该蛋白可能参与蛋白质-蛋白质和蛋白质-碳水化合物相互作用。多囊蛋白-1约30%由16个名为PKD结构域的新型蛋白质模块组成。我们在此表明,该结构域具有β-折叠结构。尽管这种折叠结构在许多细胞表面模块中很常见,但PKD结构域代表一个独特的蛋白质家族。人和河豚多囊蛋白-1的第十个PKD结构域显示出表面残基的广泛保守性,这表明该区域可能是一个配体结合位点。这一结构将有助于确定PKD1基因大部分错义突变可能产生的影响。