Loading
PDBj
メニューPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

3N5E

Crystal Structure of human thymidylate synthase bound to a peptide inhibitor

3N5E の概要
エントリーDOI10.2210/pdb3n5e/pdb
関連するPDBエントリー3N5G
関連するBIRD辞書のPRD_IDPRD_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: 21795601
DOI: 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)
構造検証レポート
Validation report summary of 3n5e
検証レポート(詳細版)ダウンロードをダウンロード

226707

件を2024-10-30に公開中

PDB statisticsPDBj update infoContact PDBjnumon