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The adaptors Grb10 and Grb14 are calmodulin-binding proteins.
- Source :
-
FEBS letters [FEBS Lett] 2017 Apr; Vol. 591 (8), pp. 1176-1186. Date of Electronic Publication: 2017 Mar 26. - Publication Year :
- 2017
-
Abstract
- We identified the Grb7 family members, Grb10 and Grb14, as Ca <superscript>2+</superscript> -dependent CaM-binding proteins using Ca <superscript>2+</superscript> -dependent CaM-affinity chromatography as we previously did with Grb7. The potential CaM-binding sites were identified and experimentally tested using fluorescent-labeled peptides corresponding to these sites. The apparent affinity constant of these peptides for CaM, and the minimum number of calcium ions bound to CaM that are required for effective binding to these peptides were also determined. We prepared deletion mutants of the three adaptor proteins lacking the identified sites and determined that they lost or strongly diminished their CaM-binding capacity following the sequence Grb7 > > Grb14 > Grb10. More than one CaM-binding site and/or accessory CaM-binding sites appear to exist in Grb10 and Grb14, as compared to a single one present in Grb7.<br /> (© 2017 Federation of European Biochemical Societies.)
- Subjects :
- Adaptor Proteins, Signal Transducing chemistry
Adaptor Proteins, Signal Transducing genetics
Amino Acid Sequence
Binding Sites
Calmodulin chemistry
Chromatography, Affinity
Conserved Sequence
GRB10 Adaptor Protein chemistry
GRB10 Adaptor Protein genetics
GRB7 Adaptor Protein chemistry
GRB7 Adaptor Protein genetics
GRB7 Adaptor Protein metabolism
Gene Deletion
HEK293 Cells
Humans
Kinetics
Mutagenesis, Site-Directed
Peptide Fragments chemistry
Peptide Fragments genetics
Peptide Fragments metabolism
Protein Conformation
Protein Interaction Domains and Motifs
Recombinant Fusion Proteins chemistry
Recombinant Fusion Proteins metabolism
Sequence Homology, Amino Acid
Structural Homology, Protein
Adaptor Proteins, Signal Transducing metabolism
Calcium Signaling
Calmodulin metabolism
GRB10 Adaptor Protein metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3468
- Volume :
- 591
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 28295264
- Full Text :
- https://doi.org/10.1002/1873-3468.12623