1984
Electron spin relaxation of CuA and cytochrome a in cytochrome c oxidase. Comparison to heme, copper, and sulfur radical complexes.
Brudvig G, Blair D, Chan S. Electron spin relaxation of CuA and cytochrome a in cytochrome c oxidase. Comparison to heme, copper, and sulfur radical complexes. Journal Of Biological Chemistry 1984, 259: 11001-11009. PMID: 6088526, DOI: 10.1016/s0021-9258(18)90613-7.Peer-Reviewed Original ResearchConceptsType 1 copperType 2 copperSulfur radicalsBlue copper proteinsMetal centerCopper complexesRadical complexesCopper centerCO complexCopper proteinsProtein environmentLow-spin heme proteinsParamagnetic sitesSpin centersHeme proteinsInorganic copperMagnetic dipolar interactionElectron spin relaxationCopperComplexesSpin-lattice relaxationDipolar interactionsCytochrome c oxidaseRadicalsCuA
1979
Resonance Raman spectra of cytochrome c oxidase. Excitation in the 600-nm region.
Bocian D, Lemley A, Petersen N, Brudvig G, Chan S. Resonance Raman spectra of cytochrome c oxidase. Excitation in the 600-nm region. Biochemistry 1979, 18: 4396-402. PMID: 226125, DOI: 10.1021/bi00587a020.Peer-Reviewed Original ResearchStructure of cytochrome a3-Cua3 couple in cytochrome c oxidase as revealed by nitric oxide binding studies.
Stevens T, Brudvig G, Bocian D, Chan S. Structure of cytochrome a3-Cua3 couple in cytochrome c oxidase as revealed by nitric oxide binding studies. Proceedings Of The National Academy Of Sciences Of The United States Of America 1979, 76: 3320-3324. PMID: 226967, PMCID: PMC383817, DOI: 10.1073/pnas.76.7.3320.Peer-Reviewed Original Research