Phosphoryl group transfer: evolution of a catalytic scaffold

被引:225
作者
Allen, KN
Dunaway-Mariano, D
机构
[1] Boston Univ, Sch Med, Dept Physiol, Boston, MA 02118 USA
[2] Univ New Mexico, Dept Chem, Albuquerque, NM 87131 USA
关键词
D O I
10.1016/j.tibs.2004.07.008
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
It is proposed that enzymic phosphoryl-transfer reactions occur by concerted, step-wise, associative (phosphorane-intermediate) or dissociative (metaphosphate-intermediate) mechanisms, as dictated by the catalytic scaffold and the reactants. During the evolution of a phosphotransferase family, the mechanism of the phosphoryl-transfer reaction is in constant flux, potentially changing with each adaptation of the catalytic scaffold to a new phosphoryl-donor-acceptor pair. Phosphotransferases of the recently discovered haloacid dehalogenase superfamily of enzymes, one of the largest and most ubiquitous of the phosphotransferase families characterized to date, are described in the context of the co-evolution of the catalytic scaffold and mechanism.
引用
收藏
页码:495 / 503
页数:9
相关论文
共 67 条
  • [1] Nucleophilic activation by positioning in phosphoryl transfer catalyzed by nucleoside diphosphate kinase
    Admiraal, SJ
    Schneider, B
    Meyer, P
    Janin, J
    Véron, M
    Deville-Bonne, D
    Herschlag, D
    [J]. BIOCHEMISTRY, 1999, 38 (15) : 4701 - 4711
  • [2] Allen KN, 2003, SCIENCE, V301
  • [3] Hydrolysis of phosphotriesters: Determination of transition states in parallel reactions by heavy-atom isotope effects
    Anderson, MA
    Shim, H
    Raushel, FM
    Cleland, WW
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (38) : 9246 - 9253
  • [4] The catalytic domain of the P-type ATPase has the haloacid dehalogenase fold
    Aravind, L
    Galperin, MY
    Koonin, EV
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (04) : 127 - 129
  • [5] The HD domain defines a new superfamily of metal-dependent phosphohydrolases
    Aravind, L
    Koonin, EV
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (12) : 469 - 472
  • [6] Babbitt PC, 2001, ADV PROTEIN CHEM, V55, P1, DOI 10.1016/S0065-3233(01)55001-9
  • [7] Insights into the mechanism of catalysis by the P-C bond-cleaving enzyme phosphonoacetaldehyde hydrolase derived from gene sequence analysis and mutagenesis
    Baker, AS
    Ciocci, MJ
    Metcalf, WW
    Kim, J
    Babbitt, PC
    Wanner, BL
    Martin, BM
    Dunaway-Mariano, D
    [J]. BIOCHEMISTRY, 1998, 37 (26) : 9305 - 9315
  • [8] Blackburn GM, 2003, SCIENCE, V301
  • [9] The first structure of a bacterial class B acid phosphatase reveals further structural heterogeneity among phosphatases of the haloacid dehalogenase fold
    Calderone, V
    Forleo, C
    Benvenuti, M
    Thaller, MC
    Rossolini, GM
    Mangani, S
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2004, 335 (03) : 761 - 773
  • [10] Comparisons of phosphorothioate with phosphate transfer reactions for a monoester, diester, and triester: Isotope effect studies
    Catrina, IE
    Hengge, AC
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (25) : 7546 - 7552