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1C1N

RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES

1C1N の概要
エントリーDOI10.2210/pdb1c1n/pdb
関連するPDBエントリー1C1O 1C1P 1C1Q 1C1R 1C1S 1C1T 1C1U 1C1V 1C1W 1C2D 1C2E 1C2F 1C2G 1C2H 1C2I 1C2J 1C2L 1C2M
分子名称TRYPSIN, CALCIUM ION, ZINC ION, ... (6 entities in total)
機能のキーワードzn(ii)-mediated serine protease inhibitors, ph dependence, zn(ii) affinity stucture-based drug design, serine protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Bos taurus (cattle)
細胞内の位置Secreted, extracellular space: P00760
タンパク質・核酸の鎖数1
化学式量合計23645.99
構造登録者
Katz, B.A.,Luong, C. (登録日: 1999-07-21, 公開日: 2000-07-26, 最終更新日: 2024-11-06)
主引用文献Katz, B.A.,Clark, J.M.,Finer-Moore, J.S.,Jenkins, T.E.,Johnson, C.R.,Ross, M.J.,Luong, C.,Moore, W.R.,Stroud, R.M.
Design of potent selective zinc-mediated serine protease inhibitors.
Nature, 391:608-612, 1998
Cited by
PubMed Abstract: Many serine proteases are targets for therapeutic intervention because they often play key roles in disease. Small molecule inhibitors of serine proteases with high affinity are especially interesting as they could be used as scaffolds from which to develop drugs selective for protease targets. One such inhibitor is bis(5-amidino-2-benzimidazolyl)methane (BABIM), standing out as the best inhibitor of trypsin (by a factor of over 100) in a series of over 60 relatively closely related analogues. By probing the structural basis of inhibition, we discovered, using crystallographic methods, a new mode of high-affinity binding in which a Zn2+ ion is tetrahedrally coordinated between two chelating nitrogens of BABIM and two active site residues, His57 and Ser 195. Zn2+, at subphysiological levels, enhances inhibition by over 10(3)-fold. The distinct Zn2+ coordination geometry implies a strong dependence of affinity on substituents. This unique structural paradigm has enabled development of potent, highly selective, Zn2+-dependent inhibitors of several therapeutically important serine proteases, using a physiologically ubiquitous metal ion.
PubMed: 9468142
DOI: 10.1038/35422
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.4 Å)
構造検証レポート
Validation report summary of 1c1n
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2025-04-02に公開中

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