机构:
Departments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt UniversityDepartments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt University
Benjamin A.Gilston
[1
]
Eric P.Skaar
论文数: 0引用数: 0
h-index: 0
机构:
Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical CenterDepartments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt University
Eric P.Skaar
[2
]
Walter J.Chazin
论文数: 0引用数: 0
h-index: 0
机构:
Departments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt UniversityDepartments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt University
Walter J.Chazin
[1
]
机构:
[1] Departments of Biochemistry and Chemistry, and Center for Structural Biology, Vanderbilt University
[2] Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center
The S100 proteins are a unique class of EF-hand Ca2+binding proteins distributed in a cell-specific, tissue-specific, and cell cycle-specific manner in humans and other vertebrates. These proteins are distinguished by their distinctive homodimeric structure, both intracellular and extracellular functions, and the ability to bind transition metals at the dimer interface. Here we summarize current knowledge of S100 protein binding of Zn2+, Cu2+and Mn2+ions, focusing on binding affinities, conformational changes that arise from metal binding, and the roles of transition metal binding in S100 protein function.
机构:
Univ York, Dept Chem, York Struct Biol Lab, York YO10 5DD, N Yorkshire, England
Kings Coll London, Sch Biomed & Hlth Sci, London WC2R 2LS, EnglandUniv York, Dept Chem, York Struct Biol Lab, York YO10 5DD, N Yorkshire, England