Protein kinases: evolution of dynamic regulatory proteins

被引:676
作者
Taylor, Susan S. [1 ,2 ,3 ]
Kornev, Alexandr P. [2 ,3 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
ACTIVATION LOOP PHOSPHORYLATION; CRYSTAL-STRUCTURE; CATALYTIC SUBUNIT; TYROSINE KINASE; SUBSTRATE RECOGNITION; STRUCTURAL BASIS; C-SRC; MECHANISM; ADENOSINE; REVEALS;
D O I
10.1016/j.tibs.2010.09.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukayotic protein kinases evolved as a family of highly dynamic molecules with strictly organized internal architecture. A single hydrophobic F-helix serves as a central scaffold for assembly of the entire molecule. Two nonconsecutive hydrophobic structures termed "spines" anchor all the elements important for catalysis to the F-helix. They make firm, but flexible, connections within the molecule, providing a high level of internal dynamics of the protein kinase. During the course of evolution, protein kinases developed a universal regulatory mechanism associated with a large activation segment that can be dynamically folded and unfolded in the course of cell functioning. Protein kinases thus represent a unique, highly dynamic, and precisely regulated set of switches that control most biological events in eukaryotic cells.
引用
收藏
页码:65 / 77
页数:13
相关论文
共 60 条
[51]  
2-I
[52]   Phosphorylation reaction in cAPK protein kinase-free energy quantum mechanical/molecular mechanics simulations [J].
Valiev, Marat ;
Yang, Jie ;
Adams, Joseph A. ;
Taylor, Susan S. ;
Weare, John H. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (47) :13455-13464
[53]  
WALSH DA, 1968, J BIOL CHEM, V243, P3763
[54]   PKA type IIa holoenzyme reveals a combinatorial strategy for isoform diversity [J].
Wu, Jian ;
Brown, Simon H. J. ;
von Daake, Sventja ;
Taylor, Susan S. .
SCIENCE, 2007, 318 (5848) :274-279
[55]   WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II [J].
Xu, BE ;
English, JM ;
Wilsbacher, JL ;
Stippec, S ;
Goldsmith, EJ ;
Cobb, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (22) :16795-16801
[56]   Crystal structures of c-Src reveal features of its autoinhibitory mechanism [J].
Xu, WQ ;
Doshi, A ;
Lei, M ;
Eck, MJ ;
Harrison, SC .
MOLECULAR CELL, 1999, 3 (05) :629-638
[57]   Allosteric network of cAMP-dependent protein kinase revealed by mutation of Tyr204 in the P+1 loop [J].
Yang, J ;
Garrod, SM ;
Deal, MS ;
Anand, GS ;
Woods, VL ;
Taylor, S .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 346 (01) :191-201
[58]   Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation [J].
Yang, J ;
Cron, P ;
Thompson, V ;
Good, VM ;
Hess, D ;
Hemmings, BA ;
Barford, D .
MOLECULAR CELL, 2002, 9 (06) :1227-1240
[59]   Structure of the LKB1-STRAD-MO25 Complex Reveals an Allosteric Mechanism of Kinase Activation [J].
Zeqiraj, Elton ;
Filippi, Beatrice Maria ;
Deak, Maria ;
Alessi, Dario R. ;
van Aalten, Daan M. F. .
SCIENCE, 2009, 326 (5960) :1707-1711
[60]   Through the "Gatekeeper Door": Exploiting the Active Kinase Conformation [J].
Zuccotto, Fabio ;
Ardini, Elena ;
Casale, Elena ;
Angiolini, Mauro .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (07) :2681-2694