Creatine kinase: Essential arginine residues at the nucleotide binding site identified by chemical modification and high-resolution tandem mass spectrometry

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

Volumn 95, Issue 7, 1998, Pages 3362-3365

  Wood, Troy D ^a,b   Guan, Ziqiang ^c   Borders Jr , Charles L ^d   Chen, Lorenzo H ^e   Kenyon, George L ^e   Mclafferty, Fred W ^c  

^a UNIVERSITY AT BUFFALO   (United States)

^b ROSWELL PARK CANCER INSTITUTE   (United States)

^c Department of Molecular Biology and Genetics   (United States)

^d 931 College Mall   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Electrospray ionization; Fourier transform mass spectrometry; Protein sequencing

Indexed keywords

ARGININE; CREATINE KINASE; PHENYLGLYOXAL;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BINDING SITE; CONTROLLED STUDY; CRYSTAL STRUCTURE; ENZYME MODIFICATION; ENZYME STRUCTURE; FOURIER TRANSFORMATION; NONHUMAN; NUCLEOTIDE METABOLISM; PRIORITY JOURNAL; RABBIT; STOICHIOMETRY; TANDEM MASS SPECTROMETRY;

ANIMALS; ARGININE; BINDING SITES; CREATINE KINASE; ENERGY METABOLISM; MASS SPECTROMETRY; MUSCLE, SKELETAL; NUCLEOTIDES; RABBITS;

ANIMALIA; GALLUS GALLUS; ORYCTOLAGUS CUNICULUS;

EID: 0032584106     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.7.3362     Document Type: Article

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