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Full-Text Articles in Molecular Biology
The Role Of A Conserved Serine Residue Within Hydrogen Bonding Distance Of Fad In Redox Properties And The Modulation Of Catalysis By Ca2+/Calmodulin Of Constitutive Nitric-Oxide Synthases, Satya Prakash Panda, Ying Tong Gao, Linda J. Roman, Pavel Marta´Sek, John C. Salerno, Bettie Masters
The Role Of A Conserved Serine Residue Within Hydrogen Bonding Distance Of Fad In Redox Properties And The Modulation Of Catalysis By Ca2+/Calmodulin Of Constitutive Nitric-Oxide Synthases, Satya Prakash Panda, Ying Tong Gao, Linda J. Roman, Pavel Marta´Sek, John C. Salerno, Bettie Masters
Faculty and Research Publications
The crystal structure of the neuronal nitric-oxide synthase (nNOS) NADPH/FAD binding domain indicated that Ser-1176 is within hydrogen bonding distance of Asp-1393 and the O4 atom of FAD and is also near the N5 atom of FAD (3.7Å). This serine residue is conserved in most of the ferredoxin-NADP+ reductase family of proteins and is important in electron transfer. In the present study, the homologous serines of both nNOS (Ser-1176) and endothelial nitric-oxide synthase (eNOS) (Ser-942) were mutated to threonine and alanine. Both substitutions yielded proteins that exhibited decreased rates of electron transfer through the flavin domains, in the presence …