Hydrophobic as well as Charged Residues in both MEK1 and ERK2 are Important for their Proper Docking

Journal of Biological Chemistry

Volumn 276, Issue 28, 2001, Pages 26509-26515

  Xu, Bing E ^b   Stippec, Steve ^b   Robinson, Fred L ^b   Cobb, Melanie H ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; CELLS; CYTOLOGY; HYDROPHOBICITY; MUTAGENESIS;

PHOSPHORYLATIONS; SIGNAL TRANSMISSIONS;

BIOCHEMISTRY;

MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE 1; MAP2K1 PROTEIN, HUMAN; MITOGEN ACTIVATED PROTEIN KINASE KINASE; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1; PROTEIN SERINE THREONINE KINASE;

ARTICLE; CELL NUCLEUS; CONTROLLED STUDY; CYTOPLASM; ENZYME ACTIVE SITE; ENZYME SUBSTRATE COMPLEX; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; HYDROPHOBICITY; IMMUNOFLUORESCENCE; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SITE DIRECTED MUTAGENESIS; AMINO ACID SEQUENCE; CELL LINE; CHEMISTRY; METABOLISM; MOLECULAR GENETICS; MUTATION; SIGNAL TRANSDUCTION; STRUCTURE ACTIVITY RELATION;

CERVUS ELAPHUS;

AMINO ACID SEQUENCE; CELL LINE; HUMANS; MAP KINASE KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN-SERINE-THREONINE KINASES; SIGNAL TRANSDUCTION; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0035854672     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M102769200     Document Type: Article

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