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Calmodulin (CaM), short for calcium modulated protein, is a small calcium binding protein with a three dimensional structure. Calcium is the most abundant essential mineral in the human diet for proper functioning of neurons to forming strong bones and can also serve as a second messenger for enzymes and proteins. Calmodulin has been known to be involved in various Ca2+ - dependent signal transduction pathways, can act as a Ca2+ detector, and has been involved with regulated protein-kinases ^[1].

Its importance can be exemplified by the fact that the protein has been known to be highly conserved in eukaryotes. Highly conserved structures that do not undergo significant evolutionary changes imply that the structure is mandatory for cell or organism survival and that any mutations in the genetic sequence that codes for the protein would be deleterious. The function of calmodulin is typically studied using yeast as a model organism. This is done for a variety of reasons, including the fact that yeast has a fully annotated genome with human homologues for genes associated with their ion channels, yeast is fast growing and they are heat stable^[2].

^[3].

Calmodulin in the body

Calmodulin is located and used ubiquitously, but is especially prevalent in brain and muscle tissue. Calmodulin in the cell is mainly localized in organelles and binds to Calcium which then promotes the phosphorylation of protein kinases and activation of other proteins to begin signal transduction for a variety of different pathways, mainly different forms of cell signaling. The phosphorylation of these protein-kinases occurs when Ca2+ reach about 1000 nM and initiates a rapid signaling pathway^[4].

Structural Highlights

Calmodulin has a molecular mass of 16 kilodaltons (kD) and it functions along with ryanodine receptor (RyR)^[5]. CaM consists of 148 amino acid residues that is characterized by a helix-loop-helix binding motif, also known as the EF hand ^[6]. Calmodulin has one subunit with a distinct dumbbell shape in which a linker region joins two globular domains^[7]. Calmodulin is known to undergo a conformational change upon binding with a calcium ion in which each lobe transitions from a closed conformation to an open conformation^[8]. This protein has four major, high-affinity binding sites, as shown by figure 1. The calmodulin binding region has been shown to be a series of hydrophobic amino acids (such as Trp or Leu), hydrophilic amino acids (such as Glu or Asp), and basic amino acids (such as Arg or Lys)^[9]. Calmodulin typically wraps around its target, with the two globular domains gripping either side of it. NMR studies clearly show that the connector between the two calcium binding globular domains is flexible even when it is not bound to its target proteins. However, the full range of flexibility can be seen in calmodulin interactions with its target proteins.

Function

Each end of the globular domains of CaM binds to two Calcium ions, which allows CaM to bind to a total of four Calcium ions. The conformational changes which CaM undergoes allow it to be able to bind more specifically. Calmodulin elicits a pathway signal transduction by activating protein kinases which can then go on to phosphorylate other proteins, or other proteins can directly bind to Calmodulin. This would require that the other proteins have a specific binding motif or substrate binding mechanism for Calmodulin. Because there are many different types of binding motifs used by other proteins to interact with Calmodulin, there are no conserved amino acid sequences for CaM binding.