3JAA
HUMAN DNA POLYMERASE ETA in COMPLEX WITH NORMAL DNA AND INCO NUCLEOTIDE (NRM)
3JAA の概要
| エントリーDOI | 10.2210/pdb3jaa/pdb |
| 関連するPDBエントリー | 3JA9 |
| EMDBエントリー | 6339 |
| 分子名称 | DNA polymerase eta, DNA (5'-D(*T*CP*AP*TP*TP*AP*TP*GP*AP*CP*GP*CP*T)-3, DNA (5'-D(*TP*AP*GP*CP*GP*TP*CP*AP*T)-3'), ... (7 entities in total) |
| 機能のキーワード | pol eta, polymerase, thymine dimer, cpd, xpv, xeroderma pigm variant, dna damage, transferase-dna complex, transferase/dna |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 56871.67 |
| 構造登録者 | |
| 主引用文献 | Lau, W.C.,Li, Y.,Zhang, Q.,Huen, M.S. Molecular architecture of the Ub-PCNA/Pol eta complex bound to DNA Sci Rep, 5:15759-15759, 2015 Cited by PubMed Abstract: Translesion synthesis (TLS) is the mechanism by which DNA polymerases replicate through unrepaired DNA lesions. TLS is activated by monoubiquitination of the homotrimeric proliferating cell nuclear antigen (PCNA) at lysine-164, followed by the switch from replicative to specialized polymerases at DNA damage sites. Pol η belongs to the Y-Family of specialized polymerases that can efficiently bypass UV-induced lesions. Like other members of the Y-Family polymerases, its recruitment to the damaged sites is mediated by the interaction with monoubiquitinated PCNA (Ub-PCNA) via its ubiquitin-binding domain and non-canonical PCNA-interacting motif in the C-terminal region. The structural determinants underlying the direct recognition of Ub-PCNA by Pol η, or Y-Family polymerases in general, remain largely unknown. Here we report a structure of the Ub-PCNA/Pol η complex bound to DNA determined by single-particle electron microscopy (EM). The overall obtained structure resembles that of the editing PCNA/PolB complex. Analysis of the map revealed the conformation of ubiquitin that binds the C-terminal domain of Pol η. Our present study suggests that the Ub-PCNA/Pol η interaction requires the formation of a structured binding interface, which is dictated by the inherent flexibility of Ub-PCNA. PubMed: 26503230DOI: 10.1038/srep15759 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (22 Å) |
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