3N5E
Crystal Structure of human thymidylate synthase bound to a peptide inhibitor
3N5E の概要
エントリーDOI | 10.2210/pdb3n5e/pdb |
関連するPDBエントリー | 3N5G |
関連するBIRD辞書のPRD_ID | PRD_000970 |
分子名称 | Thymidylate synthase, Synthetic peptide LR, SULFATE ION, ... (5 entities in total) |
機能のキーワード | peptide inhibitor, protein-peptide complex, interface inhibitor, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
由来する生物種 | Homo sapiens (human) 詳細 |
細胞内の位置 | Nucleus: P04818 P04818 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 75962.80 |
構造登録者 | Pozzi, C.,Cardinale, D.,Guaitoli, G.,Tondi, D.,Luciani, R.,Myllykallio, H.,Ferrari, S.,Costi, M.P.,Mangani, S. (登録日: 2010-05-25, 公開日: 2011-06-08, 最終更新日: 2023-09-06) |
主引用文献 | Cardinale, D.,Guaitoli, G.,Tondi, D.,Luciani, R.,Henrich, S.,Salo-Ahen, O.M.,Ferrari, S.,Marverti, G.,Guerrieri, D.,Ligabue, A.,Frassineti, C.,Pozzi, C.,Mangani, S.,Fessas, D.,Guerrini, R.,Ponterini, G.,Wade, R.C.,Costi, M.P. Protein-protein interface-binding peptides inhibit the cancer therapy target human thymidylate synthase. Proc.Natl.Acad.Sci.USA, 108:E542-E549, 2011 Cited by PubMed Abstract: Human thymidylate synthase is a homodimeric enzyme that plays a key role in DNA synthesis and is a target for several clinically important anticancer drugs that bind to its active site. We have designed peptides to specifically target its dimer interface. Here we show through X-ray diffraction, spectroscopic, kinetic, and calorimetric evidence that the peptides do indeed bind at the interface of the dimeric protein and stabilize its di-inactive form. The "LR" peptide binds at a previously unknown binding site and shows a previously undescribed mechanism for the allosteric inhibition of a homodimeric enzyme. It inhibits the intracellular enzyme in ovarian cancer cells and reduces cellular growth at low micromolar concentrations in both cisplatin-sensitive and -resistant cells without causing protein overexpression. This peptide demonstrates the potential of allosteric inhibition of hTS for overcoming platinum drug resistance in ovarian cancer. PubMed: 21795601DOI: 10.1073/pnas.1104829108 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.26 Å) |
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