4TWO

Human EphA3 Kinase domain in complex with compound 164

4TWO の概要

• エントリーDOI: 10.2210/pdb4two/pdb
• 分子名称: Ephrin type-A receptor 3, 5-{[3-carbamoyl-4-(3,4-dimethylphenyl)-5-methylthiophen-2-yl]amino}-5-oxopentanoic acid (3 entities in total)
• 機能のキーワード: transferase/transferase inhibitor, transferase
• 由来する生物種: Homo sapiens (Human)
• 細胞内の位置: Isoform 1: Cell membrane; Single-pass type I membrane protein. Isoform 2: Secreted: P29320
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 40832.63

構造登録者

Dong, J.,Caflisch, A. (登録日: 2014-07-01, 公開日: 2015-05-13, 最終更新日: 2023-12-20)

主引用文献

Dong, J.,Zhao, H.,Zhou, T.,Spiliotopoulos, D.,Rajendran, C.,Li, X.D.,Huang, D.,Caflisch, A.
Structural Analysis of the Binding of Type I, I1/2, and II Inhibitors to Eph Tyrosine Kinases.
Acs Med.Chem.Lett., 6:79-83, 2015

PubMed Abstract: We have solved the crystal structures of the EphA3 tyrosine kinase in complex with nine small-molecule inhibitors, which represent five different chemotypes and three main binding modes, i.e., types I and I1/2 (DFG in) and type II (DFG out). The three structures with type I1/2 inhibitors show that the higher affinity with respect to type I is due to an additional polar group (hydroxyl or pyrazole ring of indazole) which is fully buried and is involved in the same hydrogen bonds as the (urea or amide) linker of the type II inhibitors. Overall, the type I and type II binding modes belong to the lock-and-key and induced fit mechanism, respectively. In the type II binding, the scaffold in contact with the hinge region influences the position of the Phe765 side chain of the DFG motif and the orientation of the Gly-rich loop. The binding mode of Birb796 in the EphA3 kinase does not involve any hydrogen bond with the hinge region, which is different from the Birb796/p38 MAP kinase complex. Our structural analysis emphasizes the importance of accounting for structural plasticity of the ATP binding site in the design of type II inhibitors of tyrosine kinases.

PubMed: 25589935
DOI: 10.1021/ml500355x

実験手法

X-RAY DIFFRACTION (2.047 Å)