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Insights into Soluble Guanylyl Cyclase Activation Derived from Improved Heme-Mimetics
21
Citations
14
References
2013
Year
Molecular BiologyChemical BiologyEnzymatic ModificationRedox BiologyBay 58-2667 BoundHeme TraffickingNucleic Acid ChemistryImproved Heme-mimeticsNostoc SpProtein X-ray CrystallographyStructure-function Enzyme KineticsGlycosylationProtein ChemistryBiochemistryBay 58-2667 DerivativesHeme SignalingMolecular ModelingStructural BiologyNatural SciencesHeme DegradationMedicineDrug Discovery
Recently, the structure of BAY 58-2667 bound to the Nostoc sp. H-NOX domain was published. On the basis of this structural information, we designed BAY 58-2667 derivatives and tested their effects on soluble guanylyl cyclase (sGC) activity. Derivative 20 activated sGC 4.8-fold more than BAY 58-2667. Co-crystallization of 20 with the Ns H-NOX domain revealed that the increased conformational distortion at the C-terminal region of αF helix containing 110-114 residues contributes to the higher activation triggered by 20.
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