Crystal structures of two intermediates in the assembly of the papillomavirus replication initiation complex

被引:61
作者
Enemark, EJ
Stenlund, A
Joshua-Tor, L
机构
[1] WM Keck Struct Biol Lab, Cold Spring Harbor, NY 11724 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
crystal structure; DNA complexes; helicase assembly; papillomavirus; replication-initiation;
D O I
10.1093/emboj/21.6.1487
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
Initiation of DNA replication of the papillomavirus genome is a multi-step process involving the sequential loading of viral E1 protein subunits onto the origin of replication. Here we have captured structural snapshots of two sequential steps in the assembly process. Initially, an E1 dimer binds to adjacent major grooves on one face of the double helix; a second dimer then binds to another face of the helix. Each E1 monomer has two DNA-binding modules: a DNA-binding loop, which binds to one DNA strand and a DNA-binding helix, which binds to the opposite strand. The nature of DNA binding suggests a mechanism for the transition between double- and single-stranded DNA binding that is implicit in the progression to a functional helicase.
引用
收藏
页码:1487 / 1496
页数:10
相关论文
共 44 条
  • [41] 3.0.CO
  • [42] 2-F
  • [43] ACTIVATION OF BPV-1 REPLICATION INVITRO BY THE TRANSCRIPTION FACTOR E2
    YANG, L
    LI, R
    MOHR, IJ
    CLARK, R
    BOTCHAN, MR
    [J]. NATURE, 1991, 353 (6345) : 628 - 632
  • [44] YANG YD, 1993, CHIN J HYPERTENS, V1, P1