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1XTN

crystal structure of CISK-PX domain with sulfates

1XTN の概要
エントリーDOI10.2210/pdb1xtn/pdb
関連するPDBエントリー1XTE
分子名称Serine/threonine-protein kinase Sgk3, SULFATE ION (3 entities in total)
機能のキーワードcisk, px domain, transferase
由来する生物種Mus musculus (house mouse)
細胞内の位置Cytoplasmic vesicle : Q9ERE3
タンパク質・核酸の鎖数2
化学式量合計29109.17
構造登録者
Xing, Y.,Liu, D.,Zhang, R.,Joachimiak, A.,Songyang, Z.,Xu, W. (登録日: 2004-10-22, 公開日: 2004-11-02, 最終更新日: 2023-08-23)
主引用文献Xing, Y.,Liu, D.,Zhang, R.,Joachimiak, A.,Songyang, Z.,Xu, W.
Structural basis of membrane targeting by the Phox homology domain of cytokine-independent survival kinase (CISK-PX)
J.Biol.Chem., 279:30662-30669, 2004
Cited by
PubMed Abstract: The cytokine-independent survival kinase (CISK) in the serum and glucocorticoid-regulated kinase family plays an important role in mediating cell growth and survival. N-terminal to its catalytic kinase domain, CISK contains a phox homology (PX) domain, a phosphoinositide-binding motif that directs the membrane localization of CISK and regulates CISK activity. We have determined the crystal structures of the mouse CISK-PX domain to unravel the structural basis of membrane targeting of CISK. In addition to the specific interactions conferred by the phosphoinositide-binding pocket, the structure suggests that a hydrophobic loop region and a hydrophilic beta-turn contribute to the interactions with the membrane. Furthermore, biochemical studies reveal that CISK-PX dimerizes in the presence of the linker between the PX domain and kinase domain, suggesting a multivalent mechanism in membrane localization of CISK.
PubMed: 15126499
DOI: 10.1074/jbc.M404107200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 1xtn
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2026-02-04に公開中

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