Structural profiling of endogenous S-nitrosocysteine residues reveals unique features that accommodate diverse mechanisms for protein S-nitrosylation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 107, Issue 39, 2010, Pages 16958-16963

  Doulias, Paschalis Thomas ^a   Greene, Jennifer L ^a   Greco, Todd M ^a   Tenopoulou, Margarita ^a   Seeholzer, Steve H ^a   Dunbrack, Roland L ^b   Ischiropoulos, Harry ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b FOX CHASE CANCER CENTER   (United States)

Author keywords

Cysteine modification; Nitric oxide; Posttranslational modification; Proteomics; S nitrosation

Indexed keywords

CYSTEINE; METAL; METALLOPROTEIN; S NITROSOCYSTEINE; PROTEIN; PROTEOME; S NITROSOTHIOL; S-NITROSOCYSTEINE;

ALPHA HELIX; AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; BETA SHEET; CATALYSIS; HYDROPHILICITY; HYDROPHOBICITY; MOUSE; NITROSYLATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN METABOLISM; PROTEIN MODIFICATION; PROTEIN MOTIF; PROTEIN NITROSYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN SECONDARY STRUCTURE; PROTEIN STRUCTURE; PROTEOMICS; ANALOGS AND DERIVATIVES; ANIMAL; CHEMICAL PHENOMENA; CHEMISTRY; LIVER; METABOLISM; MOLECULAR GENETICS; PROTEIN PROCESSING;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; ANIMALS; CYSTEINE; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; LIVER; MICE; MOLECULAR SEQUENCE DATA; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEINS; PROTEOME; PROTEOMICS; S-NITROSOTHIOLS;

EID: 78049288138     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1008036107     Document Type: Article

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