Title of article :
Crystal Structure of Viral Macrophage Inflammatory Protein I Encoded by Kaposiʹs Sarcoma-associated Herpesvirus at 1.7 Å
Author/Authors :
John G. Luz، نويسنده , , Minmin Yu، نويسنده , , Ying Su، نويسنده , , Zining Wu، نويسنده , , Guang-Zhou Zhou، نويسنده , , Ren Sun and Allen T. Chwang ، نويسنده , , Ian A. Wilson، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Abstract :
Viral macrophage inflammatory protein I (vMIP-I) is a chemokine encoded by the Kaposiʹs sarcoma-associated herpesvirus (KSHV) that selectively activates the CC chemokine receptor 8 (CCR8), for which the endogenous ligand is CCL1. The crystal structure of vMIP-I was determined at 1.7 Å for comparison with other chemokines, especially those that bind CCR8, such as vMIP-II from KSHV, a CCR8 antagonist and the closest homolog (40% identical). vMIP-I has a typical chemokine fold consisting of an extended N-terminal loop, followed by a three-stranded antiparallel β-sheet and a C-terminal α-helix. The four molecules in the asymmetric unit comprise two MIP-1β-like dimers. Electrostatic surface representations of CCR8-binding chemokines reveal only minor areas of correlating surface potential, which must be reconciled with promiscuity in receptor and glycosaminoglycan (GAG) binding. In addition, the biological relevance of chemokine oligomerization is examined by comparing the oligomeric states of all chemokine structures deposited to date in the RCSB PDB.
Keywords :
Herpesvirus , chemotaxis , Chemokine , HIV
Journal title :
Journal of Molecular Biology
Journal title :
Journal of Molecular Biology