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1MUX

SOLUTION NMR STRUCTURE OF CALMODULIN/W-7 COMPLEX: THE BASIS OF DIVERSITY IN MOLECULAR RECOGNITION, 30 STRUCTURES

1MUX の概要
エントリーDOI10.2210/pdb1mux/pdb
分子名称CALMODULIN, CALCIUM ION, N-(6-AMINOHEXYL)-5-CHLORO-1-NAPHTHALENESULFONAMIDE (3 entities in total)
機能のキーワードcomplex (calmodulin-inhibitor), calmodulin, w-7, naphthalenesulfonamide, calcium-binding
由来する生物種Xenopus laevis (African clawed frog)
タンパク質・核酸の鎖数1
化学式量合計17563.40
構造登録者
Osawa, M.,Swindells, M.B.,Tanikawa, J.,Tanaka, T.,Mase, T.,Furuya, T.,Ikura, M. (登録日: 1997-09-06, 公開日: 1998-10-14, 最終更新日: 2024-05-22)
主引用文献Osawa, M.,Swindells, M.B.,Tanikawa, J.,Tanaka, T.,Mase, T.,Furuya, T.,Ikura, M.
Solution structure of calmodulin-W-7 complex: the basis of diversity in molecular recognition.
J.Mol.Biol., 276:165-176, 1998
Cited by
PubMed Abstract: The solution structure of calcium-bound calmodulin (CaM) complexed with an antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7), has been determined by multidimensional NMR spectroscopy. The structure consists of one molecule of W-7 binding to each of the two domains of CaM. In each domain, the W-7 chloronaphthalene ring interacts with four methionine methyl groups and other aliphatic or aromatic side-chains in a deep hydrophobic pocket, the site responsible for CaM binding to CaM-dependent enzymes such as myosin light chain kinases (MLCKs) and CaM kinase II. This competitive binding at the same site between W-7 and CaM-dependent enzymes suggests the mechanism by which W-7 inhibits CaM to activate the enzymes. The orientation of the W-7 naphthalene ring in the N-terminal pocket is rotated approximately 40 degrees with respect to that in the C-terminal pocket. The W-7 ring orientation differs significantly from the Trp800 indole ring of smooth muscle MLCK bound to the C-terminal pocket and the phenothiazine ring of trifluoperazine bound to the N or C-terminal pocket. These comparative structural analyses demonstrate that the two hydrophobic pockets of CaM can accommodate a variety of bulky aromatic rings, which provides a plausible structural basis for the diversity in CaM-mediated molecular recognition.
PubMed: 9514729
DOI: 10.1006/jmbi.1997.1524
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 1mux
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2026-04-29に公開中

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