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DOI | 10.2210/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: 9514729DOI: 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 |
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