8BD2
Calcium-bound Calmodulin variant G113R
Summary for 8BD2
Entry DOI | 10.2210/pdb8bd2/pdb |
NMR Information | BMRB: 34764 |
Descriptor | Calmodulin-3, CALCIUM ION (2 entities in total) |
Functional Keywords | calmodulin ca-binding protein ca-signalling protein, metal binding protein |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 16901.65 |
Authors | Wimmer, R.,Holler, C.V.,Petersson, N.M.,Iwai, H.,Niemelae, M.A.,Brohus, M.,Overgaard, M.T. (deposition date: 2022-10-18, release date: 2023-11-08, Last modification date: 2024-01-17) |
Primary citation | Holler, C.V.,Petersson, N.M.,Brohus, M.,Niemela, M.A.,Iversen, E.D.,Overgaard, M.T.,Iwai, H.,Wimmer, R. Allosteric changes in protein stability and dynamics as pathogenic mechanism for calmodulin variants not affecting Ca 2+ coordinating residues. Cell Calcium, 117:102831-102831, 2023 Cited by PubMed Abstract: Mutations in the small, calcium-sensing, protein calmodulin cause cardiac arrhythmia and can ultimately prove lethal. Here, we report the impact of the G113R variant on the structure and dynamics of the calmodulin molecule, both in the presence and in the absence of calcium. We show that the mutation introduces minor changes into the structure of calmodulin and that it changes the thermostability and thus the degree of foldedness at human body temperature. The mutation also severely impacts the intramolecular mobility of calmodulin, especially in the apo form. Glycine 113 acts as an alpha-helical C-capping residue in both apo/ - and Ca/calmodulin, but its exchange to arginine has very different effects on the apo and Ca forms. The majority of arrhythmogenic calmodulin variants identified affects residues in the Ca coordinating loops of the two C-domain EF-Hands, causing a 'direct impact on Ca binding'. However, G113R lies outside a Ca coordinating loop and acts differently and more similar to the previously characterized arrhythmogenic N53I. Therefore, we suggest that altered apo/CaM dynamics may be a novel general disease mechanism, defining low-calcium target affinity - or Ca binding kinetics - critical for timely coordination of essential ion-channels in the excitation-contraction cycle. PubMed: 37995470DOI: 10.1016/j.ceca.2023.102831 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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