5ETA

Structure of MAPK14 with bound the KIM domain of the Toxoplasma protein GRA24

5ETA の概要

• エントリーDOI: 10.2210/pdb5eta/pdb
• 分子名称: Mitogen-activated protein kinase 14, Putative transmembrane protein (3 entities in total)
• 機能のキーワード: mapk14, gra24, kim domain, peptide-protein complex, transferase
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 86314.66

構造登録者

Pellegrini, E.,Palencia, A.,Braun, L.,Kapp, U.,Bougdour, A.,Belrhali, H.,Bowler, M.W.,Hakimi, M. (登録日: 2015-11-17, 公開日: 2016-10-26, 最終更新日: 2024-11-13)

主引用文献

Pellegrini, E.,Palencia, A.,Braun, L.,Kapp, U.,Bougdour, A.,Belrhali, H.,Bowler, M.W.,Hakimi, M.A.
Structural Basis for the Subversion of MAP Kinase Signaling by an Intrinsically Disordered Parasite Secreted Agonist.
Structure, 25:16-26, 2017

PubMed Abstract: The causative agent of toxoplasmosis, the intracellular parasite Toxoplasma gondii, delivers a protein, GRA24, into the cells it infects that interacts with the mitogen-activated protein (MAP) kinase p38α (MAPK14), leading to activation and nuclear translocation of the host kinase and a subsequent inflammatory response that controls the progress of the parasite. The purification of a recombinant complex of GRA24 and human p38α has allowed the molecular basis of this activation to be determined. GRA24 is shown to be intrinsically disordered, binding two kinases that act independently, and is the only factor required to bypass the canonical mitogen-activated protein kinase activation pathway. An adapted kinase interaction motif (KIM) forms a highly stable complex that competes with cytoplasmic regulatory partners. In addition, the recombinant complex forms a powerful in vitro tool to evaluate the specificity and effectiveness of p38α inhibitors that have advanced to clinical trials, as it provides a hitherto unavailable stable and highly active form of p38α.

PubMed: 27889209
DOI: 10.1016/j.str.2016.10.011

実験手法

X-RAY DIFFRACTION (2.8 Å)