Isoenzyme-specific interaction of muscle-type creatine kinase with the sarcomeric M-line is mediated by NH2-terminal lysine charge-clamps

Journal of Cell Biology

Volumn 149, Issue 6, 2000, Pages 1225-1234

  Hornemann, Thorsten ^a   Stolz, Martin ^a,b   Wallimann, Theo ^a  

^a ETH ZURICH   (Switzerland)

^b Central Laboratory in Bern   (Switzerland)

Author keywords

Creatine kinase; Electrophoretic mobility shift; Isoenzyme specific association; Muscle energetics; Sarcomeric M line

Indexed keywords

BINDING PROTEIN; CREATINE KINASE BB; CREATINE KINASE MM; LYSINE;

AMINO TERMINAL SEQUENCE; ANIMAL TISSUE; ARTICLE; CHIMERA; CONTROLLED STUDY; ENZYME BINDING; ENZYME STRUCTURE; MUSCLE CELL; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; PSOAS MUSCLE; RABBIT; SARCOMERE; SEQUENCE HOMOLOGY; SKINNED MUSCLE FIBER; X RAY CRYSTALLOGRAPHY;

AMINO ACID SEQUENCE; ANIMALS; CREATINE KINASE; FLUORESCENT ANTIBODY TECHNIQUE; ISOENZYMES; LYSINE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; PROTEIN BINDING; PSOAS MUSCLES; RABBITS; RECOMBINANT FUSION PROTEINS; SARCOMERES; SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA; ORYCTOLAGUS CUNICULUS;

EID: 0034641108     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.149.6.1225     Document Type: Article

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