8E84
Human PCNA mutant- C148S
8E84 の概要
エントリーDOI | 10.2210/pdb8e84/pdb |
分子名称 | Proliferating cell nuclear antigen (1 entity in total) |
機能のキーワード | dna binding protein, sliding clamp, human |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 86339.06 |
構造登録者 | |
主引用文献 | Magrino, J.,Munford, V.,Martins, D.J.,Homma, T.K.,Page, B.,Gaubitz, C.,Freire, B.L.,Lerario, A.M.,Vilar, J.B.,Amorin, A.,Leao, E.K.E.,Kok, F.,Menck, C.F.,Jorge, A.A.,Kelch, B.A. A thermosensitive PCNA allele underlies an ataxia-telangiectasia-like disorder. J.Biol.Chem., 299:104656-104656, 2023 Cited by PubMed Abstract: Proliferating cell nuclear antigen (PCNA) is a sliding clamp protein that coordinates DNA replication with various DNA maintenance events that are critical for human health. Recently, a hypomorphic homozygous serine to isoleucine (S228I) substitution in PCNA was described to underlie a rare DNA repair disorder known as PCNA-associated DNA repair disorder (PARD). PARD symptoms range from UV sensitivity, neurodegeneration, telangiectasia, and premature aging. We, and others, previously showed that the S228I variant changes the protein-binding pocket of PCNA to a conformation that impairs interactions with specific partners. Here, we report a second PCNA substitution (C148S) that also causes PARD. Unlike PCNA-S228I, PCNA-C148S has WT-like structure and affinity toward partners. In contrast, both disease-associated variants possess a thermostability defect. Furthermore, patient-derived cells homozygous for the C148S allele exhibit low levels of chromatin-bound PCNA and display temperature-dependent phenotypes. The stability defect of both PARD variants indicates that PCNA levels are likely an important driver of PARD disease. These results significantly advance our understanding of PARD and will likely stimulate additional work focused on clinical, diagnostic, and therapeutic aspects of this severe disease. PubMed: 36990216DOI: 10.1016/j.jbc.2023.104656 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.1 Å) |
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