5F6T
Structure of calexcitin-Gd3+ complex.
Summary for 5F6T
Entry DOI | 10.2210/pdb5f6t/pdb |
Related | 2ccm |
Descriptor | Calexcitin, GADOLINIUM ATOM, CALCIUM ION, ... (4 entities in total) |
Functional Keywords | ef-hand neuronal calcium signalling, calcium-binding protein |
Biological source | Doryteuthis pealeii (Longfin inshore squid) |
Total number of polymer chains | 1 |
Total formula weight | 22538.47 |
Authors | Chataigner, L.,Guo, J.,Erskine, P.T.,Coker, A.R.,Wood, S.P.,Cooper, J.B. (deposition date: 2015-12-06, release date: 2015-12-16, Last modification date: 2024-01-10) |
Primary citation | Chataigner, L.,Guo, J.,Erskine, P.T.,Coker, A.R.,Wood, S.P.,Gombos, Z.,Cooper, J.B. Binding of Gd(3+) to the neuronal signalling protein calexcitin identifies an exchangeable Ca(2+)-binding site. Acta Crystallogr.,Sect.F, 72:276-281, 2016 Cited by PubMed Abstract: Calexcitin was first identified in the marine snail Hermissenda crassicornis as a neuronal-specific protein that becomes upregulated and phosphorylated in associative learning. Calexcitin possesses four EF-hand motifs, but only the first three (EF-1 to EF-3) are involved in binding metal ions. Past work has indicated that under physiological conditions EF-1 and EF-2 bind Mg(2+) and Ca(2+), while EF-3 is likely to bind only Ca(2+). The fourth EF-hand is nonfunctional owing to a lack of key metal-binding residues. The aim of this study was to use a crystallographic approach to determine which of the three metal-binding sites of calexcitin is most readily replaced by exogenous metal ions, potentially shedding light on which of the EF-hands play a `sensory' role in neuronal calcium signalling. By co-crystallizing recombinant calexcitin with equimolar Gd(3+) in the presence of trace Ca(2+), EF-1 was shown to become fully occupied by Gd(3+) ions, while the other two sites remain fully occupied by Ca(2+). The structure of the Gd(3+)-calexcitin complex has been refined to an R factor of 21.5% and an Rfree of 30.4% at 2.2 Å resolution. These findings suggest that EF-1 of calexcitin is the Ca(2+)-binding site with the lowest selectivity for Ca(2+), and the implications of this finding for calcium sensing in neuronal signalling pathways are discussed. PubMed: 27050260DOI: 10.1107/S2053230X16003526 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.201 Å) |
Structure validation
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