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作者:

Ke, Guo-Tao (Ke, Guo-Tao.) | Hu, Jian-Ping (Hu, Jian-Ping.) | Chen, Wei-Zu (Chen, Wei-Zu.) | Wang, Cun-Xin (Wang, Cun-Xin.)

收录:

CPCI-S

摘要:

HIV-1 integrase (IN) is an essential enzyme for viral replication cycle and a widely held assumption is that functional IN acts as a tetramer. The association of the IN tetramer with eight different length segments of viral end DNA were investigated by using DOT package. Based on the eight bindings, the DNA binding regions of IN tetramer and the influence of the length of viral DNA to the association were explored. The results indicate that there are three DNA binding regions of IN tetramer for viral DNA. Further, two regions are the viral DNA binding regions, and the rest are the host DNA binding region. All of the above simulation results agree well with experimental data, which provide us a more complete structural basis for guiding drug discovery and reveling integration mechanism.

关键词:

drug discovery HIV-1IN molecular docking tetramer

作者机构:

  • [ 1 ] [Ke, Guo-Tao]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China
  • [ 2 ] [Hu, Jian-Ping]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China
  • [ 3 ] [Chen, Wei-Zu]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China
  • [ 4 ] [Wang, Cun-Xin]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China

通讯作者信息:

  • [Wang, Cun-Xin]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China

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来源 :

PROGRESS ON POST-GENOME TECHNOLOGIES

年份: 2007

页码: 292-294

语种: 英文

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