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Bioinorganic chemistry is a field that examines the role of metals in biology. Bioinorganic chemistry includes the study of both natural phenomena such as the behavior of metalloproteins as well as artificially introduced metals, including those that are non-essential , in medicine and toxicology .
Indexed by ISI Journal of Biological Inorganic Chemistry received an impact factor of 2.538 as reported in the 2014 Journal Citation Reports by Thomson Reuters, ranking it 157 out of 289 journals in the category Biochemistry & Molecular Biology [2] and ranking it 9th out of 44 journals in the category Chemistry, Inorganic & Nuclear. [3]
The Society of Biological Inorganic Chemistry is a learned society established to advance research and education in the field of biological inorganic chemistry. It holds training courses, workshops and conferences to facilitate exchange of information between scientists involved in the research and teaching of biological inorganic chemistry.
William's work in pure inorganic chemistry led to a two-volume textbook of inorganic chemistry, written with Courtenay Phillips, [16] [17] He became increasingly interested in enzyme catalysis, and in particular the role of metal ions, as for example the role of copper in proteins. [18]
Tolman is the recipient of many awards for his research, including an ACS Award for Distinguished Service in the Advancement of Inorganic Chemistry in 2017, [25] [26] the Charles E. Bowers Teaching Award from the University of Minnesota in 2012, [27] a Alexander von Humboldt Foundation Research Award for 2004–2005, [3] a Buck-Whitney Medal ...
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Bioorganometallic chemistry is the study of biologically active molecules that contain carbon directly bonded to metals or metalloids. The importance of main-group and transition-metal centers has long been recognized as important to the function of enzymes and other biomolecules.
The 3-D structures of a number of rubredoxins have been solved. The fold belongs to the α+β class, with 2 α-helices and 2-3 β-strands. Rubredoxin active site contains an iron ion which is coordinated by the sulfurs of four conserved cysteine residues forming an almost regular tetrahedron.