3RNY
Crystal structure of human RSK1 C-terminal kinase domain
3RNY の概要
| エントリーDOI | 10.2210/pdb3rny/pdb |
| 分子名称 | Ribosomal protein S6 kinase alpha-1, SODIUM ION (3 entities in total) |
| 機能のキーワード | protein kinase, autoinhibition, transferase |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Nucleus: Q15418 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 77690.69 |
| 構造登録者 | |
| 主引用文献 | Li, D.,Fu, T.M.,Nan, J.,Liu, C.,Li, L.F.,Su, X.D. Structural basis for the autoinhibition of the C-terminal kinase domain of human RSK1. Acta Crystallogr.,Sect.D, 68:680-685, 2012 Cited by PubMed Abstract: p90 ribosomal S6 kinases (RSKs) respond to various mitogen stimuli and comprise two distinct protein kinase domains. The C-terminal kinase domain (CTKD) receives signal from ERK1/2 and adopts an autoinhibitory mechanism. Here, the crystal structure of human RSK1 CTKD is reported at 2.7 Å resolution. The structure shows a standard kinase fold, with the catalytic residues in the ATP-binding cleft orientated in optimal conformations for phosphotransfer. The inactivation of the CTKD is conferred by an extra α-helix (αL), which occupies the substrate-binding groove. In combination with previous knowledge, this structure indicates that activation of RSK1 involves the removal of αL from the substrate-binding groove induced by ERK1/2 phosphorylation. PubMed: 22683790DOI: 10.1107/S0907444912007457 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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