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  • *Genes, ras  (1)
  • American Association for the Advancement of Science (AAAS)  (1)
  • American Chemical Society
  • American Chemical Society (ACS)
  • Periodicals Archive Online (PAO)
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  • American Association for the Advancement of Science (AAAS)  (1)
  • American Chemical Society
  • American Chemical Society (ACS)
  • Periodicals Archive Online (PAO)
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1993-02-05
    Beschreibung: Mutations in Ras protein at positions Gly12 and Gly13 (phosphate-binding loop L1) and at positions Ala59, Gly60, and Gln61 (loop L4) are commonly associated with oncogenic activation. The structural and catalytic roles of these residues were probed with a series of unnatural amino acids that have unusual main chain conformations, hydrogen bonding abilities, and steric features. The properties of wild-type and transforming Ras proteins previously thought to be uniquely associated with the structure of a single amino acid at these positions were retained by mutants that contained a variety of unnatural amino acids. This expanded set of functional mutants provides new insight into the role of loop L4 residues in switch function and suggests that loop L1 may participate in the activation of Ras protein by effector molecules.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chung, H H -- Benson, D R -- Schultz, P G -- F32 GM14165/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1993 Feb 5;259(5096):806-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, University of California, Berkeley 94720.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8430333" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Animals ; Cloning, Molecular/methods ; Escherichia coli/genetics/metabolism ; GTP Phosphohydrolases/metabolism ; GTPase-Activating Proteins ; *Genes, ras ; Hydrogen Bonding ; Methionine/genetics ; Models, Molecular ; Molecular Sequence Data ; Mutagenesis, Site-Directed ; Phosphorylation ; Plasmids ; Promoter Regions, Genetic ; *Protein Conformation ; *Protein Structure, Secondary ; Proteins/metabolism ; Proto-Oncogene Proteins p21(ras)/*chemistry/*genetics/metabolism ; Recombinant Proteins/chemistry/metabolism ; ras GTPase-Activating Proteins
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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