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1NY3

Crystal structure of ADP bound to MAP KAP kinase 2

1NY3 の概要
エントリーDOI10.2210/pdb1ny3/pdb
関連するPDBエントリー1NXK
分子名称MAP kinase-activated protein kinase 2, ADENOSINE-5'-DIPHOSPHATE (2 entities in total)
機能のキーワードmap kap kinase 2, mk2, adp, kinase, ser/thr kinase, transferase
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数1
化学式量合計46056.94
構造登録者
主引用文献Underwood, K.W.,Parris, K.D.,Federico, E.,Mosyak, L.,Czerwinski, R.M.,Shane, T.,Taylor, M.,Svenson, K.,Liu, Y.,Hsiao, C.L.,Wolfrom, S.,Maguire, M.,Malakian, K.,Telliez, J.B.,Lin, L.L.,Kriz, R.W.,Seehra, J.,Somers, W.S.,Stahl, M.L.
Catalytically active MAP KAP kinase 2 structures in complex with staurosporine and ADP reveal differences with the autoinhibited enzyme
Structure, 11:627-636, 2003
Cited by
PubMed Abstract: MAP KAP kinase 2 (MK2), a Ser/Thr kinase, plays a crucial role in the inflammatory process. We have determined the crystal structures of a catalytically active C-terminal deletion form of human MK2, residues 41-364, in complex with staurosporine at 2.7 A and with ADP at 3.2 A, revealing overall structural similarity with other Ser/Thr kinases. Kinetic analysis reveals that the K(m) for ATP is very similar for MK2 41-364 and p38-activated MK2 41-400. Conversely, the catalytic rate and binding for peptide substrate are dramatically reduced in MK2 41-364. However, phosphorylation of MK2 41-364 by p38 restores the V(max) and K(m) for peptide substrate to values comparable to those seen in p38-activated MK2 41-400, suggesting a mechanism for regulation of enzyme activity.
PubMed: 12791252
DOI: 10.1016/S0969-2126(03)00092-3
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 1ny3
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2025-12-31に公開中

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