Literature DB >> 24242906

Distribution of separations between groups in an engineered calmodulin.

R F Steiner1, S Albaugh, M C Kilhoffer.   

Abstract

An engineered calmodulin (VU-9-CaM) has been prepared in which a tryptophan group is present at position 99 and a tyrosine at position 138. The tyrosine was converted to nitrotyrosine. Timedomain dynamic fluorescence measurements were made of energy transfer from the tryptophan donor to the nitrotyrosine acceptor. These were analyzed to yield the parameters characterizing the distribution of separations between the two groups, which are located on Ca(2+)-binding domains III and IV. Their mean separation is in reasonable agreement with the crystallographic value.

Entities:  

Year:  1991        PMID: 24242906     DOI: 10.1007/BF00865254

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  12 in total

1.  Evaluation of the distribution of distances between energy donors and acceptors by fluorescence decay.

Authors:  A Grinvald; E Haas; I Z Steinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1972-08       Impact factor: 11.205

2.  Conformation-dependent nitration of the protein activator of cyclic adenosine 3',5'-monophosphate phosphodiesterase.

Authors:  P G Richman; C B Klee
Journal:  Biochemistry       Date:  1978-03-07       Impact factor: 3.162

3.  Fluorescence anisotropy decay demonstrates calcium-dependent shape changes in photo-cross-linked calmodulin.

Authors:  E W Small; S R Anderson
Journal:  Biochemistry       Date:  1988-01-12       Impact factor: 3.162

4.  Simultaneous determination of intramolecular distance distributions and conformational dynamics by global analysis of energy transfer measurements.

Authors:  J M Beechem; E Haas
Journal:  Biophys J       Date:  1989-06       Impact factor: 4.033

5.  Time-resolved fluorescence study of VU-9 calmodulin, an engineered calmodulin possessing a single tryptophan residue.

Authors:  M Chabbert; M C Kilhoffer; D M Watterson; J Haiech; H Lami
Journal:  Biochemistry       Date:  1989-07-11       Impact factor: 3.162

6.  Frequency-domain measurements of the rotational dynamics of the tyrosine groups of calmodulin.

Authors:  I Gryczynski; J R Lakowicz; R F Steiner
Journal:  Biophys Chem       Date:  1988-05       Impact factor: 2.352

7.  The interaction of melittin with calmodulin and its tryptic fragments.

Authors:  R F Steiner; L Marshall; D Needleman
Journal:  Arch Biochem Biophys       Date:  1986-04       Impact factor: 4.013

8.  The determination of the separation of tyrosine-99 and tyrosine-138 in calmodulin: radiationless energy transfer.

Authors:  R F Steiner; M Motevalli-Alibadi
Journal:  Arch Biochem Biophys       Date:  1984-11-01       Impact factor: 4.013

9.  Effect of the orientation of donor and acceptor on the probability of energy transfer involving electronic transitions of mixed polarization.

Authors:  E Haas; E Katchalski-Katzir; I Z Steinberg
Journal:  Biochemistry       Date:  1978-11-14       Impact factor: 3.162

10.  Investigation of the mechanism of calcium binding to calmodulin. Use of an isofunctional mutant with a tryptophan introduced by site-directed mutagenesis.

Authors:  M C Kilhoffer; D M Roberts; A O Adibi; D M Watterson; J Haiech
Journal:  J Biol Chem       Date:  1988-11-15       Impact factor: 5.157

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  2 in total

1.  3-Nitrotyrosine as a spectroscopic probe for investigating protein protein interactions.

Authors:  Vincenzo De Filippis; Roberta Frasson; Angelo Fontana
Journal:  Protein Sci       Date:  2006-05       Impact factor: 6.725

2.  o-Nitrotyrosine and p-iodophenylalanine as spectroscopic probes for structural characterization of SH3 complexes.

Authors:  Vincenzo De Filippis; Annamaria Draghi; Roberta Frasson; Claudio Grandi; Valeria Musi; Angelo Fontana; Annalisa Pastore
Journal:  Protein Sci       Date:  2007-06-13       Impact factor: 6.725

  2 in total

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