The binding of nucleotides and metal ions to elongation factor Tu from Bacillus stearothermophilus as studied by equilibrium dialysis

Antonsson, B. and Kalbitzer, Hans-Robert and Wittinghofer, A. (1981) The binding of nucleotides and metal ions to elongation factor Tu from Bacillus stearothermophilus as studied by equilibrium dialysis. Hoppe-Seyler's Zeitschrift für physiologische Chemie 362 (6), pp. 735-743.

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Abstract

EF-Tu from B. stearothermophilus binds divalent metal ions even in the absence of guanine nucleotides. The association constants necessary for characterizing the multiple equilibria between EF-Tu, GDP and the divalent ions magnesium and manganese were determined by equilibrium dialysis. The constants are 4.6 X 10(4) M-1 and 5.4 X 10(5) M-1 for the binding of Mg2 and 1.0 X 10(5) M-1 and 1.1 X 10(6) M-1 for the binding of Mn2 to EF-Tu and EF-Tu . GDP, respectively. In the absence of divalent ions EF-Tu binds GMP, GDP and GTP with association constants of 3 x 10(3) M-1, 1.7 x 10(7) M-1 and 1.3 x 10(6) M-1, respectively. The binding of GDP in the presence of metal ions is an order of magnitude stronger than in the absence of metal ions.

Item Type:Article
Institutions: Biology, Preclinical Medicine > Institut für Biophysik und physikalische Biochemie > Prof. Dr. Dr. Hans Robert Kalbitzer
Identification Number:
ValueType
6268521PubMed ID
Classification:
NotationType
5'-Guanylic Acid/metabolismMESH
Bacterial Proteins/metabolismMESH
DialysisMESH
Geobacillus stearothermophilus/metabolismMESH
Guanine Nucleotides/metabolismMESH
Guanosine Diphosphate/metabolismMESH
Guanosine Triphosphate/metabolismMESH
KineticsMESH
Magnesium/metabolismMESH
Manganese/metabolismMESH
Peptide Elongation Factor TuMESH
Peptide Elongation Factors/metabolismMESH
Protein BindingMESH
Subjects:500 Science > 570 Life sciences
Status:Published
Refereed:Unknown
Created at the University of Regensburg:Unknown
Owner:Gertraud Kellers
Deposited On:03 Sep 2010 14:40
Last Modified:03 Sep 2010 14:40
Item ID:16419
Owner Only: item control page