4KIO

Kinase domain mutant of human Itk in complex with a covalently-binding inhibitor

4KIO の概要

• エントリーDOI: 10.2210/pdb4kio/pdb
• 分子名称: Tyrosine-protein kinase ITK/TSK, 1-[(3S)-3-{[4-(morpholin-4-ylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)pyrimidin-2-yl]amino}pyrrolidin-1-yl]prop-2-en-1-one, 1-[(3S)-3-{[4-(morpholin-4-ylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)pyrimidin-2-yl]amino}pyrrolidin-1-yl]propan-1-one, ... (6 entities in total)
• 機能のキーワード: kinase domain, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Cytoplasm: Q08881
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 123671.14

構造登録者

Somers, D.O. (登録日: 2013-05-02, 公開日: 2013-08-21, 最終更新日: 2024-10-30)

主引用文献

Harling, J.D.,Deakin, A.M.,Campos, S.,Grimley, R.,Chaudry, L.,Nye, C.,Polyakova, O.,Bessant, C.M.,Barton, N.,Somers, D.,Barrett, J.,Graves, R.H.,Hanns, L.,Kerr, W.J.,Solari, R.
Discovery of novel irreversible inhibitors of interleukin (IL)-2-inducible tyrosine kinase (Itk) by targeting cysteine 442 in the ATP pocket.
J.Biol.Chem., 288:28195-28206, 2013

PubMed Abstract: IL-2-inducible tyrosine kinase (Itk) plays a key role in antigen receptor signaling in T cells and is considered an important target for anti-inflammatory drug discovery. In order to generate inhibitors with the necessary potency and selectivity, a compound that targeted cysteine 442 in the ATP binding pocket and with an envisaged irreversible mode of action was designed. We incorporated a high degree of molecular recognition and specific design features making the compound suitable for inhaled delivery. This study confirms the irreversible covalent binding of the inhibitor to the kinase by x-ray crystallography and enzymology while demonstrating potency, selectivity, and prolonged duration of action in in vitro biological assays. The biosynthetic turnover of the kinase was also examined as a critical factor when designing irreversible inhibitors for extended duration of action. The exemplified Itk inhibitor demonstrated inhibition of both TH1 and TH2 cytokines, was additive with fluticasone propionate, and inhibited cytokine release from human lung fragments. Finally, we describe an in vivo pharmacodynamic assay that allows rapid preclinical development without animal efficacy models.

PubMed: 23935099
DOI: 10.1074/jbc.M113.474114

実験手法

X-RAY DIFFRACTION (2.18 Å)