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5MU8

HUMAN TNF-ALPHA IN COMPLEX WITH JNJ525

5MU8 の概要
エントリーDOI10.2210/pdb5mu8/pdb
分子名称Tumor necrosis factor, ~{N}4-(phenylmethyl)-~{N}4-[2-[3-(2-piperazin-1-ylpyrimidin-5-yl)phenyl]phenyl]pyrimidine-2,4-diamine (2 entities in total)
機能のキーワードtumor necrosis factor alpha, proteros biostructures gmbh, cytokine
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数48
化学式量合計867173.44
構造登録者
主引用文献Blevitt, J.M.,Hack, M.D.,Herman, K.L.,Jackson, P.F.,Krawczuk, P.J.,Lebsack, A.D.,Liu, A.X.,Mirzadegan, T.,Nelen, M.I.,Patrick, A.N.,Steinbacher, S.,Milla, M.E.,Lumb, K.J.
Structural Basis of Small-Molecule Aggregate Induced Inhibition of a Protein-Protein Interaction.
J. Med. Chem., 60:3511-3517, 2017
Cited by
PubMed Abstract: A prevalent observation in high-throughput screening and drug discovery programs is the inhibition of protein function by small-molecule compound aggregation. Here, we present the X-ray structural description of aggregation-based inhibition of a protein-protein interaction involving tumor necrosis factor α (TNFα). An ordered conglomerate of an aggregating small-molecule inhibitor (JNJ525) induces a quaternary structure switch of TNFα that inhibits the protein-protein interaction between TNFα and TNFα receptors. SPD-304 may employ a similar mechanism of inhibition.
PubMed: 28300404
DOI: 10.1021/acs.jmedchem.6b01836
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 5mu8
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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