摘要Background: Acquired immune deficiency syndrome (AIDS) has caused catastrophic consequences to human society.During the infection process, the HIV-1 gpl20 glycoprotein undergoes a series of conformational changes while sequentially interacting with its receptor and co-receptor located on the host cell surface.Although the gpl20 crystal structural cores bound and pre-bound by the CD4 are currently available, the details of dynamics involved in conformational equilibrium and transition in relation to its function have remained elusive.
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