Structural biology of the purine biosynthetic pathway

被引:167
|
作者
Zhang, Y. [1 ]
Morar, M. [1 ]
Ealick, S. E. [1 ]
机构
[1] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
关键词
Purine biosynthesis; protein evolution; ATP-grasp superfamily; PurM superfamily; amidotransferases;
D O I
10.1007/s00018-008-8295-8
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
Purine biosynthesis requires ten enzymatic transformations to generate inosine monophosphate. PurF, PurD, PurL, PurM, PurC, and PurB are common to all pathways, while PurN or PurT, PurK/PurE-I or PurE-II, PurH or PurP, and PurJ or PurO catalyze the same steps in different organisms. X-ray crystal structures are available for all 15 purine biosynthetic enzymes, including 7 ATP-dependent enzymes, 2 amidotransferases and 2 tetrahydrofolate-dependent enzymes. Here we summarize the structures of the purine biosynthetic enzymes, discuss similarities and differences, and present arguments for pathway evolution. Four of the ATP-dependent enzymes belong to the ATP-grasp superfamily and 2 to the PurM superfamily. The amidotransferases are unrelated, with one utilizing an N-terminal nucleophileglutaminase and the other utilizing a triad glutaminase. Likewise the tetrahydrofolate-dependent enzymes are unrelated. Ancestral proteins may have included a broad specificity enzyme instead of PurD, PurT, PurK, PurC, and PurP, and a separate enzyme instead of PurM and PurL.
引用
收藏
页码:3699 / 3724
页数:26
相关论文
共 50 条
  • [1] Structural biology of the purine biosynthetic pathway
    Y. Zhang
    M. Morar
    S. E. Ealick
    [J]. Cellular and Molecular Life Sciences, 2008, 65 : 3699 - 3724
  • [2] Structural genomics on the purine nucleotides biosynthetic pathway
    Sampei, Gen-ichi
    Baba, Seiki
    Kanagawa, Mayumi
    Nakagawa, Noriko
    Ebihara, Akio
    Kuramitsu, Seiki
    Kawai, Gota
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2008, 64 : C264 - C264
  • [3] Kinetic and structural investigations of channeling in the purine biosynthetic pathway
    Kappock, TJ
    Qiao, A
    Stubbe, J
    Wang, WR
    Ealick, S
    [J]. ENZYMATIC MECHANISMS, 1999, 27 : 139 - 149
  • [4] Structural biology of the nogalamycine biosynthetic pathway.
    Claesson, Magnus
    Schneider, Gunter
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2010, 66 : S119 - S119
  • [5] Structural and functional modularity of proteins in the de novo purine biosynthetic pathway
    Li, Hui
    Fast, Walter
    Benkovic, Stephen J.
    [J]. PROTEIN SCIENCE, 2009, 18 (05) : 881 - 892
  • [6] Modular evolution of the purine biosynthetic pathway
    Kappock, TJ
    Ealick, SE
    Stubbe, J
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (05) : 567 - 572
  • [7] A NEW INTERMEDIATE IN THE PURINE BIOSYNTHETIC-PATHWAY
    MUELLER, E
    MEYER, E
    RUDOLPH, J
    STUBBE, J
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 206 : 155 - ORGN
  • [8] The structural biology of biosynthetic megaenzymes
    Weissman, Kira J.
    [J]. NATURE CHEMICAL BIOLOGY, 2015, 11 (09) : 660 - 670
  • [9] The structural biology of biosynthetic megaenzymes
    Weissman K.J.
    [J]. Nature Chemical Biology, 2015, 11 (9) : 660 - 670
  • [10] A simple screening method for defects in purine biosynthetic pathway
    Schneiderka, P
    Vyskocilová, P
    Hornik, R
    Friedecky, D
    Adam, T
    [J]. CLINICA CHIMICA ACTA, 2005, 355 : S240 - S241