1YOM
Crystal structure of Src kinase domain in complex with Purvalanol A
1YOM の概要
エントリーDOI | 10.2210/pdb1yom/pdb |
関連するPDBエントリー | 1YOJ 1YOL |
分子名称 | Proto-oncogene tyrosine-protein kinase Src, 2-({6-[(3-CHLOROPHENYL)AMINO]-9-ISOPROPYL-9H-PURIN-2-YL}AMINO)-3-METHYLBUTAN-1-OL (3 entities in total) |
機能のキーワード | protein tyrosine kinase, transferase |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Cell membrane: P12931 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 65678.28 |
構造登録者 | Breitenlechner, C.B.,Kairies, N.A.,Honold, K.,Scheiblich, S.,Koll, H.,Greiter, E.,Koch, S.,Schaefer, W.,Huber, R.,Engh, R.A. (登録日: 2005-01-27, 公開日: 2006-01-27, 最終更新日: 2024-05-29) |
主引用文献 | Breitenlechner, C.B.,Kairies, N.A.,Honold, K.,Scheiblich, S.,Koll, H.,Greiter, E.,Koch, S.,Schaefer, W.,Huber, R.,Engh, R.A. Crystal structures of active SRC kinase domain complexes J.Mol.Biol., 353:222-231, 2005 Cited by PubMed Abstract: c-Src was the first proto-oncoprotein to be identified, and has become the focus of many drug discovery programs. Src structures of a major inactive form have shown how the protein kinase is rigidified by several interdomain interactions; active configurations of Src are generated by release from this "assembled" or "bundled" form. Despite the importance of Src as a drug target, there is relatively little structural information available regarding the presumably more flexible active forms. Here we report three crystal structures of a dimeric active c-Src kinase domain, in an apo and two ligand complexed forms, with resolutions ranging from 2.9A to 1.95A. The structures show how the kinase domain, in the absence of the rigidifying interdomain interactions of the inactivation state, adopts a more open and flexible conformation. The ATP site inhibitor CGP77675 binds to the protein kinase with canonical hinge hydrogen bonds and also to the c-Src specific threonine 340. In contrast to purvalanol B binding in CDK2, purvalanol A binds in c-Src with a conformational change in a more open ATP pocket. PubMed: 16168436DOI: 10.1016/j.jmb.2005.08.023 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.9 Å) |
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