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
[1]   Kinetic and catalytic mechanisms of protein kinases [J].
Adams, JA .
CHEMICAL REVIEWS, 2001, 101 (08) :2271-2290
[2]   Activation loop phosphorylation and catalysis in protein kinases: Is there functional evidence for the autoinhibitor model? [J].
Adams, JA .
BIOCHEMISTRY, 2003, 42 (03) :601-607
[3]   Dynamic features of cAMP-dependent protein kinase revealed by apoenzyme crystal structure [J].
Akamine, P ;
Madhusudan ;
Wu, J ;
Xuong, NH ;
Ten Eyck, LF ;
Taylor, SS .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 327 (01) :159-171
[4]   The RSK family of kinases: emerging roles in cellular signalling [J].
Anjum, Rana ;
Blenis, John .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (10) :747-758
[5]   A novel mode of Gleevec binding is revealed by the structure of spleen tyrosine kinase [J].
Atwell, S ;
Adams, JM ;
Badger, J ;
Buchanan, MD ;
Feil, IK ;
Froning, KJ ;
Gao, X ;
Hendle, J ;
Keegan, K ;
Leon, BC ;
Müller-Dieckmann, HJ ;
Nienaber, VL ;
Noland, BW ;
Post, K ;
Rajashankar, KR ;
Ramos, A ;
Russell, M ;
Burley, SK ;
Buchanan, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (53) :55827-55832
[6]   Activation of tyrosine kinases by mutation of the gatekeeper threonine [J].
Azam, Mohammad ;
Seeliger, Markus A. ;
Gray, Nathanael S. ;
Kuriyan, John ;
Daley, George Q. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (10) :1109-1118
[7]   VIRAL SRC GENE-PRODUCTS ARE RELATED TO THE CATALYTIC CHAIN OF MAMMALIAN CAMP-DEPENDENT PROTEIN-KINASE [J].
BARKER, WC ;
DAYHOFF, MO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (09) :2836-2839
[8]   Effects of phosphorylation of threonine 160 on cyclin-dependent kinase 2 structure and activity [J].
Brown, NR ;
Noble, MEM ;
Lawrie, AM ;
Morris, MC ;
Tunnah, P ;
Divita, G ;
Johnson, LN ;
Endicott, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8746-8756
[9]   Higher-order substrate recognition of elF2α by the RNA-dependent protein kinase PKR [J].
Dar, AC ;
Dever, TE ;
Sicheri, F .
CELL, 2005, 122 (06) :887-900
[10]   Strategies to overcome resistance to targeted protein kinase inhibitors [J].
Daub, H ;
Specht, K ;
Ullrich, A .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (12) :1001-1010