4LWC
Fragment-Based Discovery of a Potent Inhibitor of Replication Protein A Protein-Protein Interactions
4LWC の概要
エントリーDOI | 10.2210/pdb4lwc/pdb |
関連するPDBエントリー | 4LUO 4LUV 4LUZ 4LWI |
分子名称 | Replication protein A 70 kDa DNA-binding subunit, 5-[3-chloro-4-({4-[1-(3,4-dichlorophenyl)-1H-pyrazol-5-yl]benzyl}carbamothioyl)phenyl]furan-2-carboxylic acid (3 entities in total) |
機能のキーワード | ob-fold, protein-protein interaction, dna binding protein-inhibitor complex, dna binding protein/inhibitor |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Nucleus : P27694 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 14080.61 |
構造登録者 | Feldkamp, M.D.,Frank, A.O.,Kennedy, J.P.,Waterson, A.G.,Olejnczak, E.O.,Pelz, N.F.,Patrone, J.D.,Vangamudi, B.,Camper, D.V.,Rossanese, O.W.,Fesik, S.W.,Chazin, W.J. (登録日: 2013-07-26, 公開日: 2013-12-11, 最終更新日: 2023-09-20) |
主引用文献 | Frank, A.O.,Feldkamp, M.D.,Kennedy, J.P.,Waterson, A.G.,Pelz, N.F.,Patrone, J.D.,Vangamudi, B.,Camper, D.V.,Rossanese, O.W.,Chazin, W.J.,Fesik, S.W. Discovery of a potent inhibitor of replication protein a protein-protein interactions using a fragment-linking approach. J.Med.Chem., 56:9242-9250, 2013 Cited by PubMed Abstract: Replication protein A (RPA), the major eukaryotic single-stranded DNA (ssDNA)-binding protein, is involved in nearly all cellular DNA transactions. The RPA N-terminal domain (RPA70N) is a recruitment site for proteins involved in DNA-damage response and repair. Selective inhibition of these protein-protein interactions has the potential to inhibit the DNA-damage response and to sensitize cancer cells to DNA-damaging agents without affecting other functions of RPA. To discover a potent, selective inhibitor of the RPA70N protein-protein interactions to test this hypothesis, we used NMR spectroscopy to identify fragment hits that bind to two adjacent sites in the basic cleft of RPA70N. High-resolution X-ray crystal structures of RPA70N-ligand complexes revealed how these fragments bind to RPA and guided the design of linked compounds that simultaneously occupy both sites. We have synthesized linked molecules that bind to RPA70N with submicromolar affinity and minimal disruption of RPA's interaction with ssDNA. PubMed: 24147804DOI: 10.1021/jm401333u 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.61 Å) |
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