An in cellulo-derived structure of PAK4 in complex with its inhibitor Inka1

被引:55
作者
Baskaran, Yohendran [1 ]
Ang, Khay C. [1 ,2 ]
Anekal, Praju V. [1 ]
Chan, Wee L. [1 ]
Grimes, Jonathan M. [3 ,4 ]
Manser, Ed [1 ,5 ,6 ]
Robinson, Robert C. [1 ,2 ]
机构
[1] ASTAR, Inst Mol & Cell Biol, Singapore 138673, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
[3] Univ Oxford, Div Struct Biol, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[4] Diamond Light Source Ltd, Didcot OX11 0DE, Oxon, England
[5] ASTAR, Inst Med Biol, Singapore 138648, Singapore
[6] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore 117597, Singapore
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
基金
英国惠康基金;
关键词
CRYSTAL-STRUCTURE; P21-ACTIVATED KINASES; CATALYTIC SUBUNIT; PROTEIN; IDENTIFICATION; ACTIVATION; EXPRESSION; MECHANISM; REVEALS; PEPTIDE;
D O I
10.1038/ncomms9681
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
PAK4 is a metazoan-specific kinase acting downstream of Cdc42. Here we describe the structure of human PAK4 in complex with Inka1, a potent endogenous kinase inhibitor. Using single mammalian cells containing crystals 50 mm in length, we have determined the in cellulo crystal structure at 2.95 angstrom resolution, which reveals the details of how the PAK4 catalytic domain binds cellular ATP and the Inka1 inhibitor. The crystal lattice consists only of PAK4-PAK4 contacts, which form a hexagonal array with channels of 80 angstrom in diameter that run the length of the crystal. The crystal accommodates a variety of other proteins when fused to the kinase inhibitor. Inka1-GFP was used to monitor the process crystal formation in living cells. Similar derivatives of Inka1 will allow us to study the effects of PAK4 inhibition in cells and model organisms, to allow better validation of therapeutic agents targeting PAK4.
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页数:11
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