Nitration of solavent-exposed tyrosine 74 on cytochrome c triggers heme iron-methionine 80 bond disruption nuclear magnetic resonance and optical spectroscopy studies

Journal of Biological Chemistry

Volumn 284, Issue 1, 2009, Pages 17-26

  Abriata, Luciano A ^a   Cassina, Adriana ^b   Tórtora, Verónica ^b   Marín, Mónica ^b,c   Souza, José M ^b   Castro, Laura ^b   Vila, Alejandro J ^a   Radi, Rafael ^b  

^a UNIVERSIDAD NACIONAL DE ROSARIO   (Argentina)

^b DEPARTAMENTO DE BIOQUÍMICA   (Uruguay)

^c UNIVERSIDAD DE LA REPÚBLICA   (Uruguay)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; AMINO ACIDS; CELL DEATH; ELECTRON SPIN RESONANCE SPECTROSCOPY; HIGH PRESSURE LIQUID CHROMATOGRAPHY; IRON; LIGANDS; MASS SPECTROMETRY; NITRATION; NITRIC OXIDE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PH; PHOSPHOLIPIDS; PHYSIOLOGY; PORPHYRINS; PROTEINS;

ALKALINE TRANSITION; ELECTRON TRANSFER PROTEINS; MICROENVIRONMENTS; OPTICAL SPECTROSCOPY; POST-TRANSLATIONAL MODIFICATIONS; PROTEIN FUNCTIONS; SPECTROSCOPIC CHARACTERIZATION; TYROSINE NITRATION;

NUCLEAR MAGNETIC RESONANCE;

CYTOCHROME C; GLYCERYL TRINITRATE; HEME; IRON; LYSINE; METHIONINE; PEROXYNITRITE; PHENYLALANINE; TYROSINE; CARDIOLIPIN; MITOCHONDRIAL PROTEIN; PEROXYNITROUS ACID;

APOPTOSIS; ARTICLE; CIRCULAR DICHROISM; ELECTRON TRANSPORT; ENZYME PURIFICATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NITRATION; PEPTIDE MAPPING; PKA; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROCESSING; PROTON NUCLEAR MAGNETIC RESONANCE; AMINO ACID SUBSTITUTION; ANIMAL; CHEMISTRY; GENETICS; HORSE; METABOLISM; NUCLEAR MAGNETIC RESONANCE; OXIDATION REDUCTION REACTION; PH; PHYSIOLOGY; POINT MUTATION;

EQUIDAE;

AMINO ACID SUBSTITUTION; ANIMALS; APOPTOSIS; CARDIOLIPINS; CYTOCHROMES C; HEME; HORSES; HYDROGEN-ION CONCENTRATION; IRON; MITOCHONDRIAL PROTEINS; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OXIDATION-REDUCTION; PEROXYNITROUS ACID; POINT MUTATION; PROTEIN PROCESSING, POST-TRANSLATIONAL; TYROSINE;

EID: 58649095733     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M807203200     Document Type: Article

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